<![CDATA[Kaztronix: jobboards]]>

<![CDATA[Kaztronix: jobboards]]> https://JOBS.KAZTRONIX.COM/ en-us <![CDATA[Manager, Medical Operations]]> Job Summary (Primary function):
This position is responsible for the operational oversight and coordination of multiple US Medical Affairs (USMA) projects and research initiatives, including Investigator-Initiated Research (IIR) studies. The role leads study budget management activities, including Fair Market Value (FMV) assessments and budget negotiations, while supporting project planning and execution, stakeholder and vendor management, performance tracking, and the development and maintenance of project timelines, priorities, and operational metrics to support successful study execution and organizational objectives.

Essential Functions of the Job: Study Budget Management
Investigator Initiated Research (IIR) Budget Management:

Serve as the primary contact for completing IIR study budget Fair Market Value (FMV) assessment
Review, evaluate, and negotiate IIR study budgets and line-item requests with study sites to ensure alignment with FMV guidelines and organizational standards.
Partner with IIR Project Managers to review budget requests, resolve outstanding questions, and provide timely feedback to study sites.
Maintain internal budget benchmarking data and recommend updates based on market trends, historical experience, and current rates.
Prepare and distribute quarterly reports and summaries of finalized IIR study budgets.

Company Sponsored Study Budget Management:

Develop site budget templates and negotiation parameters, or review and approve CRO-developed budget templates to ensure consistency and alignment with organizational standards.
Review and provide guidance on site budget escalation requests submitted by CROs.

Additional Job Functions and Responsibilities IIR Program Submission and Review:
Supports the operational management of the US Oncology Investigator-Initiated Research (IIR) program by partnering with cross-functional stakeholders across US Medical Affairs, Clinical Development, and Alliance organizations. Facilitates communication, coordinates meetings, and maintains documentation to ensure alignment and efficient execution of program activities.
Maintains IIR tracking tools and performance metrics to provide portfolio visibility and support risk management. Additionally, supports vendor oversight activities, delivers training on IIR systems and processes, and serves as a point of contact for user support and issue resolution.
Preclinical IIR Project Management:
Provide operational support for early-stage research initiatives by coordinating study startup, activation, execution, and closeout activities. Responsibilities include contract coordination, FMV budget assessments, drug supply oversight, and related financial processes in collaboration with investigators, study sites, Legal, and other internal stakeholders.
IIR and Research Project Management:
Support the management of Investigator-Initiated Research (IIR) and studies by partnering with cross-functional team members to facilitate concept and protocol reviews and coordinate study execution, maintenance, and closeout. Ensure study activities are completed within established timelines and budgets and in accordance with policies, SOPs, and work instructions.
Monitor study progress, milestones, and deliverables, proactively identifying, escalating, and helping mitigate risks that may affect timelines, budgets, quality, or study objectives. Develop and maintain project plans, priorities, budgets, and performance metrics, while coordinating activities across internal stakeholders, CROs, vendors, and study sites. Provide operational and vendor oversight to support timely, compliant, and high-quality study execution.
Qualifications (Minimal acceptable level of education, work experience, and competency):

Bachelor s degree (B.A. Or B.S.) required.
Minimum of five years of relevant experience in pharmaceutical, biotechnology, clinical research, or related industry.
Demonstrated experience in study budget evaluation, FMV assessment, and site budget negotiation.
Demonstrated project management experience supporting clinical or Medical Affairs research.
Advanced proficiency with Microsoft Office applications, project management tools, and document management systems.
Demonstrated success in building productive relationships with diverse internal and external stakeholders through strong communication, collaboration, and interpersonal skills.
Dependable self-starter with strong organizational skills and the ability to manage competing priorities and meet strict deadlines in a highly metrics-driven environment.

Lead all clinical data management activities across Phase I III clinical trials in rare disease therapeutic areas.
Provide strategic oversight of CROs responsible for data management execution, ensuring quality, compliance, budget adherence, and on-time deliverables.
Develop, monitor, and proactively manage CRO project plans, timelines, milestones, and key performance indicators.
Serve as the primary internal data management expert and collaborate with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Medical Monitoring, Pharmacovigilance, Regulatory Affairs, Quality, and Clinical Supply teams.
Oversee study start-up activities including database design, CRF development, edit check specifications, data transfer agreements, and vendor integration.
Ensure timely review and resolution of data queries, protocol deviations, reconciliation activities, and database lock deliverables.
Review and approve key data management documentation, including Data Management Plans, CRF Completion Guidelines, Data Validation Plans, and Database Lock Checklists.
Drive continuous process improvements and implement best practices to enhance data quality, operational efficiency, and inspection readiness.
Support regulatory submissions by ensuring high-quality, inspection-ready clinical datasets and documentation.
Assess vendor performance and provide ongoing oversight to ensure contractual obligations and study timelines are met.
Partner with functional leaders to identify risks, develop mitigation strategies, and communicate project status to senior leadership.
Stay current on industry trends, regulatory expectations, and evolving data management technologies.

Qualifications Required

Bachelor's degree in Life Sciences, Computer Science, Health Sciences, or a related field;advanced degree preferred.
Minimum of 8 years of progressive clinical data management experience within the biotechnology or pharmaceutical industry.
Experience supporting clinical trials in rare disease therapeutic areas.
Strong hands-on experience with Medidata Rave, including database development, study conduct, and database lock activities.
Demonstrated success managing and overseeing CROs, including project management, timeline oversight, vendor performance, and issue escalation.
Experience managing multiple concurrent clinical studies in a fast-paced environment.
Thorough understanding of ICH-GCP, CDISC standards, FDA regulations, and global clinical data management best practices.
Strong knowledge of EDC systems, data cleaning processes, coding dictionaries, and external data reconciliation.
Excellent project management, organizational, and problem-solving skills.
Outstanding written and verbal communication skills with the ability to influence cross-functional stakeholders.

Preferred

Experience supporting early-phase and late-phase clinical development programs.
Experience with central laboratory, ePRO/eCOA, imaging, and other external clinical data sources.
Familiarity with RBQM principles and risk-based data review methodologies.
Previous experience in a small or emerging biotechnology company where collaboration across multiple functional areas is essential.

Success Profile
The successful candidate is a collaborative leader who is comfortable operating in a lean organization, balancing strategic leadership with hands-on execution. They are highly organized, proactive, and capable of building strong partnerships with internal stakeholders and external vendors to ensure clinical data are accurate, complete, and delivered on schedule.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 04 Aug 2026 00:00:00 EDT 0 <![CDATA[Clinical Outsourcing Lead]]> We are looking for a Clinical Outsourcing Lead who is collaborative, commercially minded, and quality focused to join our Strategic Clinical Partnering team in Global Clinical Sciences and Operations, based in our Raleigh (US) office.

About the role

You will help shape how this company works with external partners for clinical studies and development services. You will guide vendor selection, lead contract discussions, support budget planning, and help teams keep outsourced activities on track. You will bring clear thinking, strong partnership skills, and a practical focus on quality, value, compliance, and timelines.

Who you will work with

You will work with Clinical Outsourcing Managers, study teams, Strategic Clinical Partnering colleagues, finance, legal, procurement, quality, and external vendors. You will also connect with teams across Patient Evidence, Patient Solutions, Patient Impact, and wider development groups to support strong vendor partnerships and smooth study delivery.

What you will do

You will lead outsourcing activities for assigned clinical studies, programs, and development services.
You will manage RFI and RFP steps, vendor selection, study awards, work orders, service agreements, amendments, and confidentiality agreements.
You will lead vendor contract discussions to support quality, timelines, value, and clear accountability.
You will support budget forecasts, cost estimates, financial reviews, and annual financial planning with study and finance teams.
You will track vendor performance, spot risks early, and share clear updates with internal stakeholders.
You will coach and support Clinical Outsourcing Managers or Strategic Clinical Partnering colleagues on complex work.

For this role, we are looking for the following education, experience, and skills:

You have a bachelor s degree in science, finance, legal, business, or a related field;a master s degree is a plus.
You bring strong experience in pharma, biotech, CRO, clinical outsourcing, vendor management, or clinical development.
You have managed vendor negotiations, contracts, budgets, forecasts, and financial assessments with good results.
You understand clinical development, ICH/GCP, vendor qualification, and outsourced clinical study delivery.
You communicate clearly in English and can guide discussions, manage conflicts, and build agreement across global teams.
You are organised, adaptable, and able to manage several priorities while keeping quality, compliance, and timelines in focus.

Lead all PhV Project start-up, maintenance and closeout activities, including, but not limited to, Safety Reporting Plan review, safety database configuration/updates, regulatory/submission impact analysis, training, MedDRA upgrade, unblinding needs and EDC access request, as applicable, for clinical trials, IST/IIRs, post-marketing programs, Market Access/Research programs.
Act as Global PhV point person for key departments (e.G. Dev.Ops, Med. Affairs, Data Management, Reg. Affairs, Commercial).
Departmental support for Portfolio oversight, including during Audits and Inspections.
Assist with CAPA/audit or inspection finding investigations and compilation of data to support quality and compliance processes.
Coordinate GPRM efforts for new NDA/MAA regulatory tasks, as required.
Organize GPRM cross-department training and brainstorming sessions for new programs and/or new products.
Act as Subject Matter Expert (SME) with Business partners, PhV service providers and other CROs.
Assist with Pharmacovigilance reconciliation of databases and listings (post marketing and clinical trial sources), as required.
Assist with creating procedures (e.G. SOPs, Working Instructions, Job Aids), forms and templates in support of efficient Project Management processes.
Ensure compliance with internal procedures, regulatory requirements, and business partner agreements to ensure inspection readiness at all times.
Other responsibilities, as required and assigned by Senior management.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Master s degree in a Science or Healthcare related discipline, or equivalent.
Minimum of 6 years Pharmacovigilance experience or other equivalent clinical or pharmaceutical experience.
Minimum of 2 years Project Management experience or equivalent relevant experience .
Proficiency using safety database systems (Argus experience preferred).
Advanced knowledge of global Pharmacovigilance regulations (CFR/GVP), ICH Guidelines and Good Clinical Practices.
Excellent computer skills (i.E. Microsoft Word, Excel, Outlook, and Power Point).
Excellent ability to work effectively within a team environment.
Advanced organizational, time management, and problem-solving skills.
Ability to create and deliver presentations.
Excellent verbal and written communication skills.
Fluency in written and verbal English.

Build and maintain orchestrated ingestion pipelines for external genomics, proteomics, and other assay data sources, including source IO, table-format writers, and row-level reconciliation.
Develop and harden layered transformation models (staging, intermediate, and mart) with real-data test coverage, data-quality guardrails, and reusable, consolidated logic.
Implement clinical data ingestion and reconciliation paths against recognized standards (e.G., SDTM, ADaM), including subject and entity resolution.
Deliver supporting platform infrastructure: service APIs, CI/CD pipelines, containerized deployments, observability instrumentation, and data-warehouse performance tuning.
Extract transformation logic and business rules from legacy analytical code (e.G., R, PySpark) and reconcile them against new platform implementations.
Translate scientific and biomarker requirements from research and bioinformatics partners into durable data models and published data contracts.
Identify repetitive processes and convert them into automated workflows, guardrails, or reusable tooling including AI-assisted workflows that make future work faster.
Participate in adversarial design and code reviews, identifying edge cases and pushing back on suboptimal patterns.
Collaborate with the lead engineer on design decisions and support delivery velocity through paired working sessions and PR reviews.
Ensure all work meets reproducibility standards: CI on every PR, automated tests, and no ad-hoc notebook-based production processes.

Minimum Qualifications

AI-native engineering practice: demonstrated experience building systems and workflows around AI coding agents (Claude Code, Cursor, Codex, or equivalent) not just prompting them. You recognize when a repeated process should become an automated pipeline, when agent output needs guardrails, and when to build infrastructure that makes future work faster. Surface-level tool usage is insufficient.
Education: Bachelor's or master's degree in Computer Science, Data Engineering, Bioinformatics, or a related field.
Experience: 4+ years of professional experience in data engineering with shipped production pipelines on AWS (S3, ECS/Fargate, Redshift or equivalent MPP).
Strong proficiency in Python and SQL with working knowledge of modern data engineering libraries.
Solid, hands-on experience with dbt and a workflow orchestration tool (Dagster, Airflow, or Prefect).
Data quality instinct: track record of catching silent failures, questioning data correctness assumptions, and noticing lossy joins or incomplete deliveries.
Working understanding of lakehouse architecture patterns, ETL processes, and schema design for complex multi-modal datasets.
Comfort working with scientific, biomarker, or other complex domain data or a demonstrated ability to ramp on unfamiliar scientific domains quickly.
Ability to handle PHI-adjacent clinical data under contractor policy (background check, compliance training, VPN access).
Willingness to work within legacy codebases (R, PySpark) to extract business rules and validate new implementations.
Excellent communication skills and ability to work in an embedded pair model with tight feedback loops.

Preferred Qualifications

Experience building or maintaining tooling around AI coding agents (custom commands, subagents, evals, or guardrails) rather than only consuming them.
Direct experience with Apache Iceberg, AWS Glue Catalog, or lakehouse table formats.
Preferred fluency reading genomic data (VAF, HGVS nomenclature, VCFs, CNV/fusion semantics).
Familiarity with clinical data standards including SDTM, ADaM, and CDISC.
Pharma, clinical research, or life sciences background.
Experience with containerization (Docker/ECS) and infrastructure-as-code (CloudFormation).
Proficiency in R for interoperability with bioinformatics teams.

Conduct weekly discovery stage screening high throughput in vitro ADME assays, such as intrinsic clearance, protein and tissue binding, CYP450 inhibition, CYP450 reaction phenotyping and whole blood stability
Perform routine laboratory tasks, including reagent preparation, equipment maintenance, and supply management
With appropriate supervision, analyze, record, and archive data, prepare summary documents, and report data as needed

Minimum Requirements

Bachelor s degree in a relevant scientific discipline with up to 3 years of experience or an M.S. (industry experience preferred)
Strong preference given to candidates with hands-on experience with in vitro ADME assays
High-throughput screening and LC/MS/MS experience preferred
Hamilton robotic liquid handler experience preferred
Ability to independently manage assigned tasks while meeting timelines and quality expectations in a fast-paced work environment
Attention to detail, and effective oral and written communication skills

Gas chromatography, liquid chromatography, ion chromatography, gel permeation chromatography
Titration: Karl Fisher water, amine number, acid number, hydroxyl number, pH, sodium sulfite, ethylene glycol
Viscosity: Brookfield, Ubbelohde
UV-Vis Spectrophotomer
Total Organic Carbon Analyzer
Cloud Point
Spectrocolorimeter
Batch Record
Hydration

-GC, HPLC, IC, Titration, pH, KF Testing Preferred

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 27 Jul 2026 00:00:00 EDT 0 <![CDATA[Biospecimen Operations Manager]]> Essential Functions of the Job (Key responsibilities)

Play a key role in the communication and integration of translational medicine objectives with clinical study team members during protocol development and execution.
Serve as a member of the Translational Medicine clinical study start team;support the tactical execution of biospecimen collection and analysis during clinical protocol development, study start-up and amendments, including contribution to and review of protocols, lab manuals, and clinical laboratory documents and communicate information as required to other departments and CROs (if appropriate);take part in program meetings with central lab, clinical, operations and data management.
Contribute to activities involving the Data Management team, including eCRF set-up, database build for sites and sample tracking/reconciliation.
Particpiate in efforts to standardize nomenclature, pictograms, sample handling instructions, and resources for all central labs to ensure consistency across studies, welcoming diverse perspectives, and inclusive practices.
Coordinate with others within Translational Medicine group and external to the group to track and manage samples, projects, and deliverables.
Aid in the process development and coordination of informed consent form tracking and clinical program sample storage/tracking using in-house and commercial systems.
Participate in vendor meetings to stay informed of current and upcoming projects, innovative technologies, and vendor offerings.
Solve problems independently, contacting internal or external clients as needed, while fostering a collaborative and inclusive environment.
Must be able to prioritize workload in response to the specific needs of numerous protocols and department.
Maintain awareness of local and international regulations as pertains to protecting the privacy of personal information that may be associated with clinical samples.
Participate in process improvement initiatives. Plan and implement procedures and systems to maximize operating efficiency.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Scientific background (BS, RN, Med Tech) with a minimum of 2 years experience in clinical drug development, clinical trial execution, central lab study setup with exposure to biomarkers, pharmacokinetics or immunogenicity sample activities including sample collection procedures and logistics considerations, and exposure to informed consent language specific to the handling of human tissue specimens
An understanding of the drug development process and familiarity with clinical labs and clinical trial sites
Experience working with Contract Research Organizations (CRO)
Demonstrated knowledge of ICH and GCP
Advanced skills in Microsoft Office programs as well as good working knowledge of electronic data systems and controlled sample management systems
Detailed and precise record keeping skills are essential as well as the ability to track and resolve issues.
Excellent teamwork and ability to collaborate with cross functional teams.
Strong interpersonal, written, and verbal communication skills

Develop and execute the global clinical operations strategy aligned with corporate development objectives.
Provide leadership and oversight for all aspects of clinical trial execution, including planning, feasibility, site activation, enrollment, monitoring, vendor oversight, and study closeout.
Build, mentor, and lead a high-performing clinical operations team while fostering a culture of accountability, collaboration, and continuous improvement.
Oversee CROs and strategic vendors, establishing performance metrics and ensuring delivery against timelines, quality standards, and budgets.
Partner closely with Clinical Development, Medical Affairs, Regulatory Affairs, Biometrics, Clinical Supply, Quality Assurance, Translational Medicine, and Program Management to ensure seamless execution of clinical programs.
Lead operational planning for global, multicenter oncology studies, proactively identifying risks and implementing mitigation strategies.
Ensure compliance with ICH-GCP guidelines, applicable regulatory requirements, SOPs, and quality standards.
Develop and manage clinical operations budgets, resource planning, forecasting, and financial oversight.
Support clinical development strategy through operational input on protocol design, country selection, feasibility assessments, and study execution plans.
Contribute to due diligence activities, portfolio planning, and business development evaluations as needed.
Represent Clinical Operations in governance committees, leadership meetings, and interactions with external partners.

Qualifications

Bachelor's degree in a scientific discipline required;advanced degree (MS, PharmD, PhD, RN, or equivalent) preferred.
15+ years of progressive clinical operations experience within biotechnology and/or pharmaceutical organizations.
Significant leadership experience managing global oncology clinical trials, including Phase I III studies.
Demonstrated success leading clinical operations teams in a fast-paced biotechnology environment.
Deep understanding of oncology drug development, clinical trial regulations, ICH-GCP, FDA, EMA, and international regulatory requirements.
Strong expertise in CRO selection, vendor management, and strategic outsourcing models.
Experience managing complex clinical trial budgets and resource planning.
Excellent leadership, communication, organizational, and cross-functional collaboration skills.
Proven ability to influence executive leadership and drive operational excellence across multiple development programs.

Preferred Experience

Experience supporting first-in-human and early clinical oncology programs.
Prior experience in a clinical-stage biotechnology company.
Experience supporting regulatory inspections and clinical quality initiatives.
Familiarity with precision medicine, biomarker-driven trials, and innovative oncology study designs is highly desirable.

Leadership Competencies

Strategic thinker with strong execution capabilities.
Collaborative and transparent leadership style.
Exceptional organizational and project management skills.
Strong decision-making and problem-solving abilities.
Ability to thrive in a dynamic, entrepreneurial biotechnology environment.
Passion for improving outcomes for patients with cancer.

This is a highly visible leadership position reporting directly to the Chief Development Officer and will play a critical role in advancing the organization's oncology pipeline through operational excellence and effective cross-functional leadership.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Thu, 23 Jul 2026 00:00:00 EDT 0 <![CDATA[Business Data Analyst]]> (Primary function) We are seeking a highly analytical and proactive Business Data Analyst / PM to join our Program and Portfolio Management team (PMO) in support of reporting and analytics. This hybrid role is weighted toward business analysis (70 75% of responsibilities) with supporting project management responsibilities in an Agile environment.

The position plays a critical role in delivering business-focused reporting and analytics initiatives that enable enterprise-wide dashboards to monitor portfolio execution, study delivery, operational performance, and milestones, cross-functional dependencies, and emerging risks across the R&D portfolio.

An emphasis of this role is on clinical operations reporting and analytics ensuring that robust, actionable insights are defined and prioritized at project initiation, with solutions deliberately designed to meet both general business requirements and clearly articulated analytics/reporting needs, KPI governance, data quality expectations, and decision-making requirements from the outset. Essential Functions of the Job ( Key responsibilities) Primary Responsibilities:
Business Analysis:

Lead requirements elicitation and analysis for Development Operations and Clinical Operations reporting and analytics initiatives, with particular emphasis on defining operational metrics, KPI definitions, data sources, and reporting requirements upfront.
Partner closely with Development Operations, Clinical Operations, portfolio management, and functional stakeholders to understand strategic objectives, key performance indicators (KPIs), operational decision-making needs, and insight gaps then translate these into clear, prioritized reporting/analytics requirements.
Initiate projects with a strong analytics-first mindset: identify the critical portfolio, study, site, study participant, milestone, resourcing, and risk questions the business needs answered, define target dashboards, reports, metrics, and data flows before detailed solutioning begins.
Drive solution design that intentionally delivers both core business functionality and high-value, reliable reporting/analytics capabilities.
Create detailed business requirements, user stories, process flows, data models, metric definitions, and analytics specifications that guide system configuration, data engineering, and PowerBI development work for Development Operations and Clinical Operations use cases.

Reporting & Analytics Leadership:

Serve as the primary advocate for analytics and reporting excellence within projects.
Work with stakeholders to establish success criteria that include measurable improvements in insight availability, data accuracy, timeliness, usability, and adoption of clinical operations reports and dashboards.
Collaborate closely with data engineering and PowerBI teams to ensure end-to-end data flows support the agreed analytics vision.
Facilitate validation of reporting outputs during user acceptance testing (UAT) to confirm business and analytical requirements are fully met.

Stakeholder Engagement & Change Enablement:

Build strong partnerships with business leaders, portfolio managers, study teams, and functional teams to align priorities and ensure analytics/reporting needs are understood and championed.
Develop and deliver training, user guides, and communication plans to drive adoption of new/enhanced reporting capabilities and system functionality.

General Project Management & Business Analysis Duties:

Support change management, UAT coordination, and post-implementation reviews focused on both operational success and realization of reporting/analytics benefits.
Contribute to continuous improvement of Agile practices, portfolio management utilization, and overall analytics maturity within the Strategic Portfolio and Project Management team.

Skills Required:

Demonstrated experience defining and driving analytics/reporting requirements from project inception through delivery.
Solid understanding of Agile methodologies and proficiency with Azure DevOps.
Experience working with data engineering teams, clinical operations data sources, data lakes, and visualization tools (PowerBI highly preferred).
Excellent requirements elicitation, analytical thinking, stakeholder management, and communication skills.

Other Skills:

Strong business acumen with a natural orientation toward data-driven insights and measurable business outcomes.
Proactive, organized, and able to manage complexity across multiple stakeholders and technical teams.
Excellent communicator who can translate complex analytics/reporting needs into clear requirements and vice versa.

Additional Skills Preferred:

Certifications: CBAP, PMI-PBA, PMP, Agile/Scrum (CSM/PSM), or BI-related certifications (e.G., Microsoft Certified: Data Analyst Associate).
Prior experience in pharmaceutical, biotech, or regulated R&D environments, with emphasis on Development Operations, Clinical Operations, clinical trial execution, or study delivery reporting.
Familiarity with data modeling, ETL concepts, and dashboard/report design principles.

Qualifications (Minimal acceptable level of education, work experience, and competency)

Bachelor s degree in mathematics, Statistics, Computer Science, Social/Physical/Life Science, Information Systems, Analytics, Project Management, Business, or related field and Minimum three (3) years experience in data analytics
4 6+ years of experience in business analysis, with at least 2 years in a role with significant focus on Development Operations, Clinical Operations, R&D portfolio reporting, analytics, and/or business intelligence

Provide medical leadership for global oncology clinical development programs across Phase I, II, III, and IV clinical trials.
Lead the medical strategy, design, and execution of clinical trial protocols supporting early and late-stage development programs.
Serve as the Medical Monitor for assigned clinical studies, providing oversight of patient safety, protocol adherence, eligibility assessments, and emerging safety signals.
Collaborate with Clinical Operations, Regulatory Affairs, Biometrics, Translational Medicine, Pharmacovigilance, Medical Affairs, and other cross-functional stakeholders to ensure successful study execution.
Contribute to clinical development plans, target product profiles, and overall program strategy.
Analyze and interpret clinical efficacy, safety, pharmacokinetic/pharmacodynamic, and biomarker data to support key development decisions.
Prepare and review clinical study reports, investigator brochures, regulatory submissions, scientific publications, abstracts, and presentations.
Support interactions with global regulatory agencies and contribute to regulatory submissions and responses.
Develop and maintain relationships with key opinion leaders, investigators, and academic collaborators.
Represent clinical programs at investigator meetings, advisory boards, and scientific congresses.
Ensure all clinical activities comply with ICH-GCP guidelines, applicable regulatory requirements, and company SOPs.

Required Qualifications

MD or DO required.
Board certification in Medical Oncology or Hematology/Oncology.
Minimum of 10 years of pharmaceutical, biotechnology, or clinical drug development experience in oncology.
Demonstrated expertise in either:
- Hematologic malignancies, or
- Solid tumor oncology.
Extensive experience leading global Phase I, II, III, and IV oncology clinical trials.
Proven experience serving as a Medical Monitor for oncology studies.
Strong understanding of oncology drug development, clinical trial methodology, regulatory requirements, and Good Clinical Practice (GCP).
Experience collaborating with global regulatory agencies, including FDA and EMA.
Ability to interpret complex clinical and scientific data and translate findings into development strategy.
Outstanding communication, leadership, and cross-functional collaboration skills.
Ability to work independently in a fast-paced, matrixed global environment.

Preferred Qualifications

Fifteen or more years of clinical and/or biopharmaceutical industry experience.
Experience in Early Clinical Development, including first-in-human, dose-escalation, and proof-of-concept studies.
Experience in immuno-oncology, targeted therapies, antibody-based therapeutics, cell therapy, or precision medicine.
Previous experience supporting regulatory filings, including NDA and/or BLA submissions.
Established relationships with global oncology investigators and key opinion leaders.

Contract Details

Position: Senior Medical Director Consultant
Duration: 6 12 months
Therapeutic Area: Oncology
Function: Early Clinical Development
Clinical Trial Scope: Global Phase I, II, III, and IV studies
Work Arrangement: Remote or hybrid (based on project needs)
Travel: Approximately 15 25% for investigator meetings, scientific congresses, and internal team meetings.

Ideal Candidate
The successful consultant is a seasoned physician leader with extensive experience in global oncology drug development and a passion for advancing innovative therapies. This individual is a strategic thinker who thrives in a collaborative, cross-functional environment and brings the clinical expertise necessary to lead complex global development programs from early clinical research through late-stage development.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 20 Jul 2026 00:00:00 EDT 0 <![CDATA[Laboratory Technician (entry level)]]> Description:
As a Formulation Laboratory Technician, you will play a crucial role in the development of various consumer products. Working in our state-of-the-art laboratory facility, you will be responsible for formulating small batches of products and conducting rigorous testing to ensure their quality and efficacy.

Key Responsibilities:
- Formulate small batches of various consumer products, including but not limited to personal care items, household products, and cosmetics.
- Conduct comprehensive testing of formulated batches to assess their performance and stability. This includes testing for viscosity, pH levels, stability under various conditions, and overall product performance evaluation.
- Collaborate closely with cross-functional teams, including Research & Development, Quality Assurance, and Manufacturing, to ensure seamless product development processes.
- Maintain detailed records of formulations, testing procedures, and results, adhering to strict documentation standards.
- Stay updated on industry trends, scientific advancements, and regulatory requirements relevant to product formulation.

Requirements:
- Bachelor's degree in a Scientific Discipline, such as Chemistry, Chemical Engineering, or related field.
- Demonstrated experience in academic or industrial settings with pH and viscosity testing techniques.
- Previous experience in personal care or consumer product formulation is preferred but not required.
- Strong attention to detail and analytical skills, with the ability to troubleshoot and problem-solve independently.
- Excellent communication and collaboration skills, with the ability to work effectively in a team environment.
- Flexibility and adaptability to work in a fast-paced, dynamic environment, prioritizing multiple tasks effectively

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Fri, 17 Jul 2026 00:00:00 EDT 0 <![CDATA[Communications Network Engineer]]> Evaluate communication hardware and software, as well as troubleshoot Local Area Networks/Base Area Networks/Wide Area Networks (LAN/BAN/WAN), and other network related problems. Administer LAN/BAN/WANs. Schedule conversions and cutovers. Coordinate with all responsible users and sites. Specialized experience in the performance and configuration of networks as well as the integration and testing of complex large-scale computer integrated networks. Must possess an Original Equipment Manufacturer (OEM) network support certification such as a Cisco Certified Network Associate (CCNA).

Required:
Sec+ (Day 1)
CCNA (w/ in 6 months of being hired)
Active ability to work in closed spaces.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Fri, 17 Jul 2026 00:00:00 EDT 0 <![CDATA[Senior Non-Clinical Editor]]> Job Summary
This position is responsible for overall quality control (QC) review and submission-ready publishing of nonclinical documents. The Senior Nonclinical Editor will copyedit/proofread, format, and perform internal consistency review of document content in accordance with company SOPs and processes to ensure documents meet required standards. This role will support all documents written by authors from Drug Metabolism and Biopharmaceutics (DMB), Chemistry Manufacturing and Controls (CMC), Toxicology (Tox), and Translational Sciences. This position may also assist in clinical document QC and publishing tasks when appropriate to meet submission timelines. The Senior Nonclinical Editor performs the activities with minimal oversight needed.

Summary of the Essential Functions of the Job

Perform internal document QC review of nonclinical documents (eg, DMB, CMC, TOX, TRS, PRECLIN) to ensure compliance with the Style Guide, template formatting, and submission ready standards.
Copyedit/proofread for grammar, style, and formatting according to AMA and style guides.
Ensure internal consistency and confirm that data are reported correctly, statements accurately reflect a common message and text to tables, figures, and appendices are accurate and consistently presented.
Check the reference list in documents, including verifying citation information via PubMed, ordering copies of references, and adding to the electronic document management system (EDMS), and ensuring each reference is cross-referenced in the document.
Proofread documents against the standard templates to ensure compliance with required sections and text.
Perform publishing of PDF documents to submission-ready standards. May involve multiple document compilation of PDF files to include appendices.
Assist Medical Writing Operations staff with clinical document QC and publishing, as appropriate.
Participate in process improvement initiatives and support Medical Writing staff with other tasks, as appropriate.
May interact cross-functionally to support clinical and nonclinical processes and template updates.

Minimum Requirements

Bachelor s degree in English, Basic Science, Business, or other analytical field with 4 years related experience in the pharmaceutical industry OR 8+ years of experience in a discipline directly related to document production (eg, medical writing, QC, editing, publishing).
Strong working knowledge of the editorial and publishing activities within Clinical Development.
Proficient in Microsoft Word, including the ability to format tables, insert cross-references, apply styles, and use templates. Experience with PowerPoint, Excel, Visio, Adobe.
Strong working knowledge of Adobe PDF bookmarking and internal/external hyperlinking to meet submission-ready standards.
Experience in the use of an EDMS (eg, Veeva Vault or SharePoint).
Ability to effectively communicate with vendors and manage outsourced editorial work.
Keen attention to detail.
Ability to manage multiple activities, prioritize effectively, and work in a fast-paced, deadline-driven environment.
Strong organizational and time management skills.
Strong verbal, written, and interpersonal communication skills.

Author, edit, and manage clinical documents supporting Phase 2 and Phase 3 oncology clinical trials, including:
- Clinical Study Protocols and protocol amendments
- Investigator Brochures (updates)
- Clinical Study Reports (CSRs)
- Informed Consent Forms
- Clinical sections of briefing books and meeting packages
- Safety narratives and integrated clinical summaries, as needed
Contribute to regulatory documents including:
- IND submissions and amendments
- Responses to Health Authority information requests
- Annual reports
- Other regulatory documents as required
Manage writing activities for 2 3 concurrent clinical studies while balancing competing priorities and timelines.
Lead document planning, timelines, and cross-functional review cycles from document kickoff through finalization.
Collaborate with subject matter experts to translate complex scientific and clinical information into clear, accurate, and submission-ready documents.
Ensure documents comply with ICH, GCP, company SOPs, and applicable regulatory guidance.
Incorporate statistical outputs, clinical data, and safety information into clear scientific narratives.
Coordinate document reviews, reconcile comments, and maintain version control throughout document development.
Support preparation for regulatory interactions and major clinical milestones.
Contribute to process improvements, document templates, and writing standards appropriate for a growing biotechnology organization.

Qualifications

Advanced degree (PharmD, PhD, MD, MS, MPH, or equivalent scientific discipline) preferred;Bachelor's degree with significant relevant experience will be considered.
5 8+ years of medical writing experience in biotechnology, pharmaceutical industry, or CRO.
Demonstrated experience authoring clinical documents for Phase 2 and Phase 3 clinical trials.
Oncology clinical development experience required.
Experience preparing Clinical Study Reports and clinical study protocols required.
Working knowledge of regulatory submission documents (INDs, briefing documents, annual reports, responses to health authorities).
Strong understanding of ICH E3, ICH E6, GCP, and FDA/EMA regulatory expectations.
Ability to independently manage multiple writing projects with minimal supervision.
Excellent project management, organization, and communication skills.
Experience working within cross-functional clinical development teams.
Proficiency with Microsoft Office and document management systems;familiarity with electronic document review platforms preferred.

Preferred Qualifications

Experience supporting late-stage oncology development programs.
Experience with immuno-oncology, virology, or targeted therapies is a plus.
Experience supporting global clinical studies.
Familiarity with submission publishing processes and electronic Common Technical Document (eCTD) structure.

Success in This Role
The successful candidate will:

Produce high-quality clinical and regulatory documents that meet aggressive development timelines.
Effectively manage writing activities across 2 3 active clinical studies simultaneously.
Build strong partnerships with cross-functional stakeholders while driving documents to completion.
Adapt comfortably within a collaborative, fast-moving biotech environment where flexibility and initiative are highly valued.
Maintain scientific rigor, attention to detail, and regulatory compliance across all deliverables.

This position offers the opportunity to make a meaningful impact within a growing clinical-stage biotechnology company, contributing directly to the advancement of innovative oncology therapies through pivotal stages of clinical development.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Wed, 08 Jul 2026 00:00:00 EDT 0 <![CDATA[Cyber Operations Specialist]]>
This role is 100% on site in the Herndon, VA area and requires a full scope poly.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 07 Jul 2026 00:00:00 EDT 0 <![CDATA[Staff Engineer Medical Devices]]> Staff Engineer, Additive Manufacturing , to support spine-focused medical device R&D through end-to-end titanium laser powder bed fusion (LPBF) prototyping and product development.
This position is hybrid 3 Days on Site based out of our Raynham, MA office location.

The Staff Engineer will support the development and optimization of Additive Manufacturing processes and products for R&D. Specifically, this role will own the additive manufacturing loop from defining and creating the build files, identifying ideal print slicing specifications, some printer operation activities, and structured feedback into subsequent design iterations.
This position is best suited for an engineer who is comfortable operating metal AM equipment, applying DfAM principles, and working within a regulated medical device development environment.
A key focus of the position is expanding the team s AM capabilities, with the Staff Engineer collaborating closely with cross functional teams including Manufacturing Innovation, Quality, Validation, and Maintenance. The role involves developing and supporting value stream projects, ensuring alignment, standardization, and best practice implementation across the network.

You will be responsible for:

Lead end to end Additive Manufacturing process development and industrialization for complex processes and New Product Introductions (NPI), ensuring scalable, robust, and validated manufacturing processes.
- Create, modify, and optimize LPBF build files for titanium medical implants including: Part orientation and nesting strategy
- Support generation and optimization to balance surface quality and removability
- Thermal management considerations for distortion-sensitive implant geometries.
- Review CAD models for printability, manufacturability, and risk, providing DfAM feedback tailored to spine implants (e.G., lattice development, fixation features, anatomical surfaces).
- Maintain build documentation consistent with R&D and design control expectations.
- Be familiar with LPBF Printer Operations including Machine setup, calibration, and pre-build checks
- Titanium powder handling, recycling, and traceability
- Build execution, monitoring, and first-level troubleshooting
- Part Removal, Post-Processing & Inspection
- Identify print anomalies relevant to implant manufacturing (distortion, support failure, surface defects).
- Support continuous improvement of AM processes, SOPs, and internal best practices for medical titanium printing.
- Perform preliminary inspection and documentation: Visual inspection and defect classification
- Basic dimensional verification
- Identification of risks impacting downstream testing (mechanical, fatigue, coating, etc.)
- Prototype Feedback & R&D Iteration
- Provide clear, structured feedback from each build to inform: Design revisions
- Build orientation and support changes
- Parameter and layout refinements
- Partner closely with Spine R&D engineers, Designers, and manufacturing teams to accelerate prototype learning cycles.
- Lead cost reduction and productivity initiatives (scrap/rework reduction, throughput improvements, consumables optimization) with measurable savings and sustainability impacts.
- Provide technical mentorship to engineers and technicians, champion continuous improvement culture, and support capability development across the organization.

Qualifications:

Bachelor s degree or equivalent experience in Engineering (or equivalent).
Demonstrated 4-6 years of experience in a relevant engineering role
Demonstrated ability in additive manufacturing/process engineering
3+ years of hands-on experience with metal additive manufacturing, preferably LPBF.
Demonstrated experience creating metal AM build files (support design, part orientation, part slicing specifications, part layout).
Experience operating industrial LPBF printers, from build file setup to completed build.
Strong experience in structured problem solving and root cause analysis.
Excellent technical content skills (specifications, validation protocols, change control).
Experience leading multi-functional teams and influencing collaborators at multiple levels.
Proven experience supporting NPI, scale-up and transfer activities.

Preferred Qualifications & Experience (Nice to Haves)
Experience specifically with titanium spinal implants or orthopedic medical devices.
Familiarity with LPBF printing platforms, experience with 3DS printing platforms preferred
Experience with build prep software such as 3Dxpert, Materialise Magics, EOSPRINT, Netfabb, nTopology, or similar.
Exposure to post-processing steps commonly used in medical devices (heat treatment, HIP, surface finishing).
Familiarity with calibration, maintenance practices and working closely with in-house maintenance teams.
Knowledge of regulatory requirements and submissions applicable to medical device manufacturing.
Prior experience mentoring/leading emerging engineers or small technical teams.]]> Tue, 07 Jul 2026 00:00:00 EDT 0 <![CDATA[Director, HR Operations]]>
Let s talk about some of the key responsibilities of the role:
People Systems (HRIS)

Own the strategy, roadmap, and governance of HR systems, ensuring alignment with business needs and future growth.
Lead implementation, optimization, and integration of HR technologies, partnering closely with IT and external vendors.
Ensure data integrity, system security, and compliance across all platforms.
Develop and enhance reporting and analytics capabilities to support data-driven decision making.
Evaluate and recommend new technologies to improve scalability, automation, and employee experience .

People Operations & Onboarding

Oversee core People Operations processes including onboarding, offboarding, employee data management, and lifecycle transactions.
Design and implement scalable, efficient, and compliant processes that enhance the employee experience.
Ensure adherence to federal, state, and local employment laws and regulatory requirements

Establish and maintain standard operating procedures and documentation across People Operations.
Lead the design and delivery of a best-in-class onboarding experience that drives early engagement and productivity.
Partner with Talent Acquisition, HR Business Partners, and hiring managers to ensure seamless new hire integration.
Partner with Finance and Total Rewards to support processing of new hire and employee stock grants, ensuring accurate data entry, timely approvals, and compliance with company equity plan guidelines.
Owns employee safety programs and compliance tracking, including WVPP and behavioral risk management activities, training, investigations, and documentation under the IIPP.

Process Optimization & Automation

Identify opportunities to streamline and automate HR processes through systems and technology.
Drive continuous improvement initiatives to increase operational efficiency and reduce manual work.
Implement scalable solutions that support organizational growth and evolving business needs.

Data, Reporting, AI & Compliance

Develop and maintain HR dashboards, metrics, and reporting frameworks.
Leverage advanced analytics and emerging AI capabilities to generate predictive insights (e.G., attrition risk, workforce planning, hiring efficiency) and enhance decision-making.
Partner with IT and Data teams to evaluate, implement, and govern AI-enabled tools within HR systems, ensuring ethical use, data privacy, and compliance.
Identify opportunities to automate reporting, workflows, and employee interactions through AI and intelligent automation.
Ensure accuracy, accessibility, and governance of people data.
Support audits, compliance reporting, and regulatory requirements in partnership with Legal and Finance.

Project Management & Cross-Functional Partnership

Lead cross-functional projects involving HR systems, processes, and transformation initiatives.
Apply strong project management and change management methodologies to ensure successful execution.
Partner with IT, Finance, Legal, and business leaders to align priorities, timelines, and deliverables.
Develop and implement change initiatives that drive organizational effectiveness and adoption.

People Leadership

Lead, coach, and develop a high-performing People Systems and Operations team, fostering a culture of accountability, innovation, and continuous improvement.
Set clear goals and priorities, providing regular feedback, development opportunities, and performance management.
Build organizational capability by attracting, developing, and retaining top talent within the function.
Establish team operating rhythms, KPIs, and success metrics aligned to business objectives.
Promote a best-in-class service-oriented mindset focused on delivering exceptional employee and stakeholder experiences.
May perform other related duties as required and/or assigned.

Factors for Success:

Bachelor s degree in Human Resources, Business Administration, Information Systems, or related discipline required;Master s degree preferred.
15+ years of progressive HR experience with a strong focus on HRIS and People Operations.
Strong understanding of HR compliance, data governance, and employee lifecycle processes.
Strong technical proficiency across HR systems and tools (e.G., HRIS, reporting tools, Excel, and related technologies).
Demonstrates business acumen, connecting People Systems and Operations priorities to broader organizational goals and compliance requirements.

Competencies

Decision Making: Makes timely, well-informed decisions using data and stakeholder input;communicates rationale clearly and navigates ambiguity with sound judgment.
Collaboration & Team Building: Builds strong cross-functional relationships, fosters trust and open dialogue, and enables effective collaboration across teams.
Outcome Driven: Translates organizational goals into clear priorities and delivers results despite changing business needs, balancing execution with team development.
Innovative Mindset and Action: Encourages experimentation and continuous improvement, applying sound judgment to scale solutions that enhance team and organizational performance.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Fri, 26 Jun 2026 00:00:00 EDT 0 <![CDATA[SQL Database Administrator]]> A Global Defense Contractor is seeking a SQL Database Administrator to provide expertise to a federal client in support of their mission critical systems in defense of our Homeland. Your role will involve overseeing database administration, performance tuning, troubleshooting, and ensuring the availability, integrity, and security of our SQL databases.

This role is onsite in Colorado Springs, CO and requires an active Secret security clearance.

Job-Essential Duties and Responsibilities: - Administer and maintain SQL Server database environments, including installation, configuration, and patch management.
- Administer and maintain database operational status and performance monitoring.
- Administer and maintain database replication monitoring and fault correction.
- Monitor database performance, identify bottlenecks, and implement optimization strategies to ensure optimal throughput and responsiveness.
- Perform database design, data modeling, and schema management to support application requirements and performance goals.
- Implement and maintain database security measures, including user access controls, data encryption, and auditing mechanisms.
- Conduct database capacity planning and forecasting to accommodate future growth and changing business requirements.
- Develop and maintain database backup and recovery strategies to ensure data availability and integrity.
- Collaborate with development teams to optimize SQL queries, database code, and stored procedures for improved performance.
- Create and maintain documentation related to database configurations, procedures, and troubleshooting guides.
- Other tasks as assigned

Job-Specific Minimum Requirements:
- An active Secret Clearance is required
- Due to contract requirements, only US Citizens can be considered. Candidates with dual citizenship cannot be considered.
- 7+ years of experience with database administration or related technologies.
- 5+ years of experience with SQL.
- Candidates must reside within a commutable distance for daily onsite work and on-call requirements.
- This contract supports systems that require 24x7x365 uptime. Candidates must be willing and able to meet recall requirements, including participation in a rotational on-call schedule.
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 23 Jun 2026 00:00:00 EDT 0 <![CDATA[Senior Manager/Associate Director, Regulatory CMC Consultant (REMOTE)]]>
Regulatory Strategy & Execution

Lead Global Strategy: Formulate innovative, accelerated CMC regulatory strategies for Client advanced therapy medicinal products (ATMPs), focusing on AAV-mediated gene therapies, antisense oligonucleotides (ASOs), and alternative CNS platforms.

Lifecycle Filings: Lead the authoring, technical review, and global submission of high-quality CMC sections (Module 2 and Module 3) for INDs, IMPDs, CTAs, and future BLAs/MAAs.

Agency Interactions: Direct or support formal interactions, briefing document preparation, and Type B/C meetings with the FDA, EMA, and other major health authorities on complex gene therapy manufacturing topics.

Regulatory Intelligence: Track evolving global regulations impacting cell and gene therapies, including FDA tissue-specific guidance, GMO applications in Europe, and expedited designations (e.G., RMAT, PRIME).

Technical Operations & Quality Collaboration

Matrix Leadership: Serve as the core regulatory CMC expert on cross-functional project teams, closely partnering with internal Quality Assurance, Process Development, and Analytical Development teams.

CDMO Oversight: Provide regulatory guidance to external Contract Development and Manufacturing Organizations (CDMOs) regarding vector manufacturing, analytical comparability protocols, stability testing, and validation protocols.

Risk Management: Conduct critical regulatory risk assessments for technical changes in manufacturing processes, scale-up protocols, or analytical method transfers, offering robust mitigation strategies.

Job Requirements & Qualifications

Experience Levels

Senior Manager: 6 to 9+ years of experience in biotech/pharma Regulatory Affairs CMC or related technical roles.

Associate Director: 10 to 12+ years of relevant experience, with a proven track record of leading regulatory submissions independently.

Technical & Scientific Profile

Advanced Biologics Expertise: Deep, hands-on regulatory experience with advanced modalities. Direct experience with viral vectors (AAV, Lentivirus), cell/gene therapies, or complex biologics is strictly required .

CNS Familiarity: Prior experience navigating the specific CMC challenges of CNS therapies (e.G., low volume/high potency fill-finish parameters, intrathecal delivery specifications) is highly preferred.

Global Regulatory Proficiency: Comprehensive fluency with FDA, EMA, and ICH requirements regarding GMP, analytical validation, and eCTD structure.

Agile Mindset: Thrives in a lean organizational structure backed by external networks;must possess excellent written communication skills and the autonomy to manage diverse external consultants.

Education

Minimum Required: Bachelor s degree in molecular biology, biochemistry, chemical engineering, or a related life sciences discipline.

Preferred: Advanced degree (Ph.D., PharmD, or MS) with focused research or industry experience in gene transfer technology.

Core Competencies & Culture Fit

Mission Alignment: Passionate about bringing transformative therapeutics to patients with neurogenetic conditions and rare diseases.

Agility & Ownership: Willing to move seamlessly between writing technical summaries and setting high-level strategic alignment with global venture partners.

Strategic Communication: The ability to explain intricate, highly technical manufacturing data to regulatory reviewers, non-profit foundations, and executive board members.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Thu, 18 Jun 2026 00:00:00 EDT 0 <![CDATA[Supply Demand Planner]]> Demand Planner is responsible for developing and maintaining accurate demand forecasts for all our brands. This role sits at the center of Sales, Supply Chain and Operations, acting as the bridge between commercial ambition and operational reality. While forecasting remains a core responsibility, success in this role will come from influencing stakeholders, driving planning discipline, and turning data into actionable business insights. In collaboration with cross-functional teams, the demand planner will gather information on factors that may impact demand, monitor actual sales performance against forecast and refine forecasts based on changing customer promotional need.

Demand Forecast Accuracy
- Improve and maintain statistical forecast models to create accurate demand forecasts for all product categories
- Manage outlier detection, maintain base and promotional forecasts coming from TPM system into GIB
- Evaluate the results of the statistical forecast at customer, warehouse, package, material level and make the necessary adjustment to reflect the most appropriate demand forecast results
- Flag significant variances between statistical forecasts and RSM-entered demand plans to improve accuracy
- Proactively use trend analysis, forecast vs actual results and data input of volume by utilizing customer promotional calendars, history and current information
Internal Processes
- Lead the demand planning meetings, prepare and present analysis This role will partner with the Sales VP, Sales Strategy team and Regional Sales Managers to gather data and transfer information into the demand plan
- Work with the sales and supply team to ensure that they ve reached consensus upon a demand plan.
- Challenge assumptions and provide data-driven recommendations
- Prepare and lead the monthly demand alignment meetings between Sales, Finance and Supply Leadership
- Navigate through complex business processes with understanding of upstream (commercial) and downstream (supply planning, manufacturing and logistics) implications
- Collaborate closely with Supply Planners to maintain up-to-date information on capacity, capability, supplier constraints in the supply network
Product Lifecycle Management
- Own product lifecycle management and distribution tracker to ensure that any add/delete items are promptly updated in the system to avoid impacting forecast accuracy
- Ensure changes in Supply Chain (SKU/Material Intro and deletion, Distribution/Network changes) are managed end-to-end including forecast needs, re-alignment requirements of sales history, maintenance of planning tables and other master data fields in SAP
- Ensure the flow of customer specific demand plans through the planning process and enterprise software tools (TPM, GIB, Clearview etc.) and provide item specific input into the monthly S&OP process
Innovation and Learning
- Contribute to continuous enhancement in the long-term demand planning process
- Continuously look for opportunities to improve processes, identify issues and provide recommendations for improvement
- Propose and implement solutions to improve demand forecast accuracy

Experience Needed:
- Bachelor's degree preferred, preferably in Supply Chain Management, Finance, Operations Management or Engineering
- 5 years experience in demand planning within FMCG business
- Strong forecast, supply planning experience
- Project management experience preferred
- Experience with MS Office Suite
- Strong understanding of supply chain management, logistics, and inventory
- Proficiency in using demand planning and forecasting software such as SAP/S4Hana, IBP, O9, Blue Planner, Blue Yonder, Kinaxis is highly preferred
- Proficiency in analyzing large sets of data and using data visualization tools to identify trends, patterns, and insight Power BI, Tableau is beneficial
- Self-starter mentality with the ability to work independently
- Excellent oral and written communication
- Prior Client experience
- Detail orientated]]> Sun, 14 Jun 2026 00:00:00 EDT 0 <![CDATA[Deployed Support Specialist Mid]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Fri, 12 Jun 2026 00:00:00 EDT 0 <![CDATA[Deployed Support Specialist Mid]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Fri, 12 Jun 2026 00:00:00 EDT 0 <![CDATA[Sr. Director, HCP Strategy - Immunology]]> Job Description
Key Responsibilities

Lead TA/indication-level HCP strategy for all approved and emerging indications. Define clear indication positioning, customer segmentation, and messaging frameworks that align to clinical data and access realities.

Translate clinical and market insights into actionable commercial strategies balancing brand-level cohesion with TA/indication-level differentiation.

Own the HCP strategic engagement roadmap from positioning to call-to-action ensuring clarity, focus, and differentiation in every HCP touchpoint.

Partner with Field Leadership to strengthen executional excellence, including message flow, call quality, and account-level customization.

Drive insight-to-action cycles using call data, CRM analytics, and field feedback loops.

Ensure the HCP experience connects seamlessly with the patient journey for unified storytelling.

Lead effective MLR/PRC engagement and pre-alignment strategies to translate complex clinical data into compelling, compliant promotional narratives.

Collaborate with Medical Affairs to integrate new data, evolving science, and emerging insights into educational content.

Drive cross-functional alignment across cross functional teams including Medical, Access, Field, and Analytics

Act as the HCP strategic counterpart to the Omnichannel (HCP + Patient) Marketing Lead, ensuring brand strategy informs journey design and content orchestration.

Qualifications

Bachelor s degree required;advanced degree or MBA preferred.

12+ years in pharmaceutical or biotech marketing, with leadership experience across HCP strategy, field promotion, and digital innovation.

Demonstrated success leading multi-indication or lifecycle brands, preferably in immunology, specialty, or rare disease.

Deep understanding of HCP engagement models, market access landscape and distribution channels

Has experience leading teams and managing direct reports

Proven experience collaborating with Omnichannel or Integrated Marketing functions to align strategy and execution.

Strong track record in peer-to-peer programming and field readiness.

Excellent communication, influence, and executive presence skills.

Cultural Attributes

Leads with tact and influence demonstrates judgment, composure, and balance under pressure;communicates with clarity and respect even amid differing viewpoints.

Acts with scientific integrity and patient-first focus in every decision.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 08 Jun 2026 00:00:00 EDT 0 <![CDATA[Director, Omnichannel Strategy & Execution]]> Key Responsibilities
Strategy & Experience Design

Define and lead the omnichannel engagement strategy across HCP and patient segments, ensuring all campaigns ladder up to unified customer journeys.

Partner with HCP and Patient marketers to translate brand strategy into personalized experiences across digital and non-digital channels (email, field, social, search, media, portals, events).

Architect end-to-end journey frameworks from audience segmentation to message sequencing and touchpoint orchestration.

Build channel-specific playbooks and frameworks for both patient and HCP engagement, rooted in behavioral insights and customer data.

Align with sales, TLL and commercial effectiveness teams to ensure coordinated experiences across all interaction points.

Data-Driven Personalization & Next Best Action (NBA)

Champion data-driven marketing through actionable insights, audience triggers, and dynamic segmentation.

Lead design and rollout of NBA and journey orchestration frameworks across brands ensuring relevance, timing, and consistency across touchpoints.

Partner with analytics and data science to define how insights, predictive models, and experimentation (A/B testing, multivariate) inform customer experiences.

Leverage data/insights to optimize message cadence, content selection, and channel prioritization.

Channel Leadership & Performance

Own the channel strategy ensuring optimal mix, budget allocation, and performance measurement across HCP and patient programs.

Continuously assess channel effectiveness and evolve the engagement mix using real-time insights.

Collaborate with paid media, CRM, content, and field teams to ensure orchestration and consistency.

Evaluate and introduce new channels and technologies to drive reach, engagement, and personalization at scale.

Cross-Functional Leadership

Serve as the key bridge between marketing, data, analytics, and digital innovation functions.

Partner with HCP and patient leads to embed omnichannel thinking into annual and tactical brand plans.

Represent omnichannel marketing on enterprise digital councils and innovation forums.

Qualifications

10+ years in pharmaceutical or healthcare marketing, with 4+ years in omnichannel or digital strategy leadership roles.

Proven expertise in channel strategy, journey design, and data-driven marketing.

Experience operationalizing NBA, customer segmentation, or personalization programs.

Strong understanding of HCP and patient engagement dynamics, content strategy, and compliance in a regulated environment.

Excellent leadership, storytelling, and cross-functional collaboration skills.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 08 Jun 2026 00:00:00 EDT 0 <![CDATA[Deputy Chief Compliance Officer]]>
Responsibilities

Leverage knowledge of industry guidance, laws, codes and best practices to direct the design, implementation, and evolution of a comprehensive US Compliance Program, ensuring alignment with the OIG and DOJ guidelines

Proactively plan for emerging trends in compliance, anticipating the impact of these trends on Company processes and controls

Serve as a strategic advisor to Commercial, Medical Affairs, Patient Advocacy, R&D and other teams to enable innovation while proactively addressing compliance risks

Partner with cross functional stakeholders to understand changing business practices, identify risks and adapt Compliance program elements to address emerging risks

Chair the US Compliance Committee and provide regular updates to the Chief Compliance Officer, Oncology on program effectiveness, risk profiles, and mitigation strategies

Lead the strategic development and implementation of a practical and business-oriented compliance training and communication program to empower Company personnel to manage risk with clarity, integrity and sound judgement

Lead the development and maintenance of a US policy framework designed to establish clear, comprehensive and effective policies and procedures to aid the business in efficient decision making. Oversee initiatives to enhance policy accessibility

Establish effective business processes and controls to ensure the Company is complying with its legal and regulatory obligations and undertake a continuous improvement process to timely identify and remediate any program gaps

Set an appropriate tone of integrity and raise awareness of compliance as a collective responsibility of all Company personnel through effective engagement, training, auditing, and monitoring

Partner with Head of Compliance Risk and Assurance to (i) identify monitoring needs, provide support for live monitoring and pull through monitoring results/analytics to business stakeholders;(ii) conduct planning and inputs for risk assessments;(iii) support annual transparency reporting;and (iv) support internal investigations

Partner with business stakeholders in connection with the preparation of an annual compliance work plan

Support various enterprise-wide initiatives led by Global Compliance function

Manage, coach and develop assigned staff and third party resources

Qualifications

Bachelor degree is required (a JD or other advanced degree or course of study strongly preferred)

Minimum of 12 years of broad compliance experience in the pharmaceutical or biotechnology industry with at least 5 years in a senior leadership position.

Exceptional working knowledge of laws, regulations, and industry guidance that affect the pharmaceutical industry

Ability to mentor and retain a high-performing team of compliance professionals, fostering a culture of continuous learning and professional accountability.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 01 Jun 2026 00:00:00 EDT 0 <![CDATA[Director/Senior Director, Biostatistical Programming]]> The Director/Senior Director, Biostatistical Programming will provide strategic and operational leadership for statistical programming across clinical development programs. This individual will serve as the senior-most programming leader within Biometrics, reporting directly to the Head of Biometrics, and will oversee a high-performing team of approximately 12 15 statistical programmers supporting multiple studies and regulatory submissions.

The successful candidate will drive programming standards, processes, innovation, and execution excellence across all phases of development while partnering closely with Biostatistics, Data Management, Clinical Development, Regulatory, and external vendors. This role requires a strong leader with deep technical expertise, global regulatory submission experience, and the ability to build scalable programming capabilities in a fast-paced biotechnology environment.
Key Responsibilities

Lead, mentor, and develop a team of approximately 12 15 statistical programmers, including managers, senior programmers, and contractors.

Serve as the functional head of Statistical Programming and primary programming representative within Biometrics leadership.

Provide strategic oversight for programming activities supporting clinical trials, integrated analyses, regulatory submissions, publications, and health authority interactions.

Establish and maintain programming standards, SOPs, processes, and best practices aligned with industry and regulatory expectations.

Ensure high-quality and timely delivery of SDTM, ADaM, TLFs, datasets, and submission packages across development programs.

Drive consistency and efficiency through automation, innovation, and implementation of modern programming technologies and workflows.

Collaborate closely with Biostatistics leadership on study design, analysis planning, resource forecasting, and submission strategy.

Oversee CRO and vendor programming activities, including governance, quality oversight, timelines, and deliverables.

Provide strategic input into regulatory submissions, inspections, and responses to health authority questions.

Partner cross-functionally with Clinical Development, Data Management, Medical Writing, Regulatory Affairs, and Clinical Operations to ensure alignment across programs.

Build and maintain a scalable organizational structure to support portfolio growth and evolving business needs.

Contribute to departmental strategy, budget planning, hiring, and long-term capability development.

Foster a culture of quality, accountability, collaboration, and continuous improvement.

Qualifications

Advanced degree in Statistics, Biostatistics, Computer Science, Mathematics, or related scientific discipline preferred.

12+ years of statistical programming experience within the biotechnology, pharmaceutical, or CRO industry, including leadership experience.

Prior experience leading global programming teams and managing direct reports.

Extensive hands-on expertise with SAS and CDISC standards (SDTM, ADaM).

Strong knowledge of regulatory requirements and submission standards for FDA, EMA, and other global health authorities.

Proven experience supporting NDA/BLA/MAA submissions and regulatory inspections.

Demonstrated ability to lead programming strategy across multiple concurrent clinical development programs.

Strong project management, communication, and stakeholder management skills.

Experience working in a fast-paced, matrixed, and highly collaborative environment.

Knowledge of R, automation platforms, or modern data science/programming approaches is a plus.

Leadership Competencies

Strategic and enterprise-minded leadership approach

Strong people development and coaching capabilities

Ability to influence across functions and organizational levels

Operational excellence with attention to quality and execution

Collaborative, solution-oriented mindset

Ability to balance strategic thinking with hands-on leadership

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 26 May 2026 00:00:00 EDT 0 <![CDATA[MQ Senior Engineer]]> This role is on-site in Annapolis Junction, MD and requires an active Secret Clearance.
Job-Specific Essential Duties and Requirements:
- Design, implement, and maintain the IBM MQ infrastructure, including queue managers, channels, queues, and other MQ objects.
- Configure and manage MQ clustering, multi-instance queue managers, and high availability solutions to ensure message reliability and fault tolerance.
- Monitor and analyze MQ performance metrics, identify bottlenecks, optimizing configurations, and tuning MQ settings to enhance system efficiency.
- Provide technical guidance and support to application developers, assisting in the integration of applications with MQ messaging.
- Ensure the security and integrity of MQ infrastructure, implementing appropriate access controls, encryption, and auditing mechanisms.
- Perform capacity planning and forecasting to ensure scalability and performance of MQ infrastructure.
- Stay updated on the latest IBM MQ versions, patches, and industry best practices, making recommendations for upgrades and improvements.
- Document technical configurations, procedures, and troubleshooting steps for the MQ environment.
- Other tasks as assigned.

Job-Specific Minimum Requirements:
- Active Secret security clearance.
- Due to contract requirements, only US Citizens can be considered. Candidates with dual citizenship cannot be considered.
- 12+ years of relevant work experience required - At least 5+ years Unix experience required
- At least 5+ years DevOps/ Infrastructure as Code (IaC) experience required - Candidates must reside within a commutable distance for daily onsite work and on-call requirements.
- This contract supports systems that require 24x7x365 uptime. Candidates must be willing and able to meet on-call requirements, including participation in a rotational on-call schedule, if required.

Preferred Skills and Qualifications:
- Bachelor's degree in relevant field or equivalent experience preferred
- Certified in IBM System Admin for MQ
- Team player, fast learner with ability to work proactively and independently to support mission critical operations supporting geographically diverse locations.
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 26 May 2026 00:00:00 EDT 0 <![CDATA[Director, Regulatory Medical Writing Consultant]]> Remote | Oncology | NDA Submissions | FDA-Facing Leadership

A growing oncology-focused biopharmaceutical organization is seeking an experienced Director of Regulatory Medical Writing to support late-stage regulatory submission activities for its endometrial cancer program. This is a highly visible, strategic role with the opportunity to evolve into a submission lead position for a critical oncology asset.

The ideal candidate will possess a strong blend of deep clinical foundational knowledge, advanced regulatory writing expertise, and meaningful experience interacting directly with the FDA. This individual will initially partner closely with Regulatory Affairs leadership and will have the opportunity to become the lead writer on the program once they demonstrate strong clinical understanding and effectiveness in regulatory and FDA-facing activities.
Key Responsibilities

Lead the planning, development, and authoring of regulatory submission documents in support of NDA filings

Drive preparation and ownership of key Module 2 documents and summaries

Support regulatory strategy and document integration for oncology programs

Collaborate cross-functionally with Regulatory Affairs, Clinical Development, Biostatistics, Clinical Operations, and related teams

Participate in FDA interactions, regulatory responses, and submission-related communications

Ensure all documents are scientifically accurate, strategically aligned, and compliant with FDA and ICH requirements

Mentor and provide guidance to junior medical writers and CSR-focused writing teams

Contribute to regulatory writing process improvements and best practices

Qualifications

Advanced scientific degree required (PhD, PharmD, MD, or equivalent)

Significant regulatory medical writing experience within biotech, pharma, or CRO environments

Oncology experience required

Strong hands-on experience authoring and leading NDA submissions, particularly Module 2 documentation

Deep clinical foundational experience required

Demonstrated experience with heavy FDA interaction, including submission support, regulatory communications, and agency-facing activities

Ability to independently manage complex writing projects and timelines in a fast-paced environment

Excellent communication, collaboration, and leadership skills

Preferred Experience

Experience mentoring or overseeing junior writers or vendors

Familiarity with oncology indications

Proven ability to operate strategically within cross-functional regulatory teams

Additional Information

Fully remote opportunity

Primarily focused on US regulatory submissions

European submission experience is not required

Open to candidates from CRO environments

Opportunity to grow into a lead regulatory writing role with increased submission ownership and FDA visibility

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Fri, 22 May 2026 00:00:00 EDT 0 <![CDATA[Medical Director, Rheumatology - Clinical Development]]> An innovative biotechnology organization focused on immune-mediated and inflammatory diseases is seeking an experienced Rheumatologist to serve as Medical Director within Clinical Development. This physician leader will play a critical role in advancing therapeutic programs from early development through late-stage clinical studies by providing strategic medical leadership, scientific expertise, and cross-functional collaboration.

The position requires deep knowledge of rheumatologic and autoimmune diseases, strong clinical judgment, and experience contributing to drug development programs in biotechnology or pharmaceutical settings.

Key Responsibilities

Provide medical leadership for rheumatology and immunology clinical development programs.

Lead the clinical strategy and execution of Phase I IV clinical trials in autoimmune and inflammatory diseases.

Author and review clinical protocols, investigator brochures, clinical study reports, safety narratives, and regulatory documents.

Collaborate with translational medicine and biomarker teams to integrate precision medicine strategies into development programs.

Serve as the medical monitor for clinical studies, including safety review and adverse event assessment.

Interpret and communicate clinical data to internal stakeholders, investigators, regulatory agencies, and external partners.

Support interactions with regulatory authorities, ethics committees, and institutional review boards.

Develop relationships with key opinion leaders, investigators, academic collaborators, and advocacy organizations in rheumatology.

Contribute to publication strategy, scientific presentations, and congress activities.

Partner closely with clinical operations, biostatistics, regulatory affairs, pharmacovigilance, medical affairs, and research teams.

Monitor competitive landscape, emerging therapies, and scientific advancements relevant to autoimmune and inflammatory diseases.

Provide strategic input for indication selection, lifecycle planning, and portfolio development.

Qualifications

MD or DO with board certification in Rheumatology.

Active medical license preferred.

Minimum of 5 8 years of clinical experience in rheumatology and/or biotechnology or pharmaceutical industry experience.

Prior experience in clinical development, medical monitoring, or translational medicine strongly preferred.

Strong understanding of autoimmune disease biology, immunology, and inflammatory pathways.

Experience designing and managing clinical trials in rheumatologic or immunologic diseases.

Familiarity with FDA, EMA, ICH-GCP, and global regulatory requirements.

Demonstrated ability to analyze complex clinical and scientific data.

Excellent communication, leadership, and cross-functional collaboration skills.

Ability to thrive in a fast-paced, innovation-driven environment.

Preferred Experience

Rheumatoid arthritis

Lupus and systemic autoimmune diseases

Fibrotic and inflammatory disorders

Biologic therapies and immune-targeted treatments

Biomarker and translational research integration

Early-stage biotechnology or emerging therapeutic platforms

Leadership Competencies

Strategic scientific thinking

Collaborative leadership

Strong medical and ethical judgment

Data-driven decision making

Effective stakeholder engagement

Adaptability and innovation mindset

Work Environment

Highly collaborative and mission-driven culture

Opportunity to shape Client therapies in immunology and inflammation

Cross-functional engagement with research and executive leadership

Hybrid or remote work flexibility based on organizational needs

Compensation & Benefits

Competitive executive-level compensation

Annual performance bonus eligibility

Equity participation or long-term incentive plans

Comprehensive health and wellness benefits

Retirement savings options

Generous paid time off and continuing education support

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Wed, 20 May 2026 00:00:00 EDT 0 <![CDATA[Sr. Process Engineer]]> In this role, you will serve as a technical leader in pharmaceutical manufacturing by driving process development, optimization, and scale-up efforts that support the reliable production of clinical and commercial drug products. You will ensure processes meet regulatory standards and contribute to cross-functional initiatives that enhance operational performance, product quality, and compliance in a highly regulated environment.

The Senior Process Engineer will also:

Lead and execute scale-up, optimization, and technology transfer projects, collaborating with Research and Development (R&D) to implement processes into large-scale manufacturing.

Serve as a subject matter expert on key unit operations and equipment, including, blending, dry granulation, wet granulation, fluid bed drying, Wurster/fluid bed coating, tableting, film coating, spray drying.

Design and execute experiments to optimize pharmaceutical formulations and processes, using design of experiments (DoE), one-factor-at-a-time approaches, and risk-based planning.

Develop and manage documentation including Performance Qualification (PQ) protocols, risk assessments, Standard Operating Procedures (SOPs), and Manufacturing Batch Records for developmental and clinical use and development reports.

Conduct process validation, cleaning validation, and perform gap analyses, Failure Modes and Effects Analyses (FMEAs), and risk assessments to ensure compliance with current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) guidelines, United States Pharmacopeia (USP), International Society for Pharmaceutical Engineering (ISPE), and International Organization for Standardization (ISO) standards.

Analyze process data, perform capability studies, and design experiments to support new product implementation and continuous improvement.

Investigate and implement workflow and equipment improvements to enhance accuracy, efficiency, and reliability across departments.

Provide technical support and troubleshooting expertise to maintenance and operations teams for equipment and process issues.

Author manufacturing deviations and Corrective and Preventive Actions (CAPAs), and lead technical risk assessments to support quality and regulatory compliance.

Train process engineers and manufacturing personnel on equipment, procedures, and safety practices.

Apply Lean Manufacturing principles and manage projects to deliver results on time and within budget.

Professional Conduct and Workplace Culture: Ensure full-time attendance, exhibit professionalism with business associates, and align daily actions with organizational values.

Perform all other duties as assigned.

Education and Experience

Bachelors in engineering, science or related field

Minimum Required: 10 plus years in regulated pharmaceutical organization that includes solid dose formulations OR Masters in an engineering discipline and 5 years of related experience

Preferred: Process engineering and validation background.

Knowledge, Skills, and Abilities

Demonstrates initiative and reliability by independently completing tasks that support team objectives and operational goals.

Communicates clearly, respectfully, and effectively across departments to relay technical information, responsibilities, and policies.

Apply critical thinking and problem-solving skills to evaluate complex issues from multiple perspectives and implement practical solutions.

Collaborate effectively in cross-functional teams to support manufacturing operations and process development activities.

Utilizes electronic management systems for equipment tracking and quality documentation, with working knowledge of current Good Manufacturing Practices (cGMP) and United States Food and Drug Administration (FDA) regulations.

Apply engineering principles to support the operation, troubleshooting, and optimization of production equipment, contributing to process reliability and efficiency.

Maintains adaptability and accountability in a regulated environment, ensuring compliance and continuous improvement in support of clinical and commercial manufacturing.

Proficiency in Microsoft Suite including Word, Excel, PowerPoint, and role related software.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 12 May 2026 00:00:00 EDT 0 <![CDATA[Senior Systems Engineer (DoD Cleared Integration & Technical Leadership)]]> We are supporting a DoD program seeking a Senior Systems Engineer to lead and support the design, integration, and implementation of complex IT solutions across a multi-technology environment. This role will help drive technical direction, support system improvements, and ensure alignment with mission and operational requirements.

This is a strong fit for someone with a deep engineering background who has taken on technical leadership responsibilities and contributed to system design efforts, while remaining hands-on.
Responsibilities

Lead and support the design, integration, and implementation of IT systems across multiple platforms and technologies

Coordinate technical efforts across teams to ensure alignment with system requirements and project goals

Contribute to system design discussions and long-term technical planning

Evaluate and recommend technologies, tools, and solutions to improve system performance and scalability

Develop and maintain system documentation, technical plans, and design artifacts

Support project planning efforts including scope, timelines, and implementation approaches

Review system designs to ensure efficiency, scalability, and proper integration

Troubleshoot and help resolve complex system and performance issues

Interface with cross-functional teams to address production and technical challenges

Mentor junior engineers and provide guidance on engineering best practices

Required Qualifications

Active Secret clearance

IAT Level II certification (Security+ or equivalent)

5-8+ years of experience in systems engineering, infrastructure engineering, or related field

Experience supporting DoD or federal IT environments

Strong experience with system integration and enterprise environments

Experience contributing to system design or technical direction

Preferred Qualifications

Experience leading technical teams or serving as a senior/lead engineer

Familiarity with system architecture concepts and enterprise design principles

Exposure to security, information assurance, or compliance frameworks

Experience supporting complex or mission-critical environments

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Thu, 30 Apr 2026 00:00:00 EDT 0 <![CDATA[Systems Engineer II (DoD Cleared Infrastructure & Integration Support)]]> We are supporting a DoD program seeking a cleared Systems Engineer to support system integration, infrastructure environments, and ongoing design efforts. This role will work alongside senior engineers to support system improvements, documentation, and operational alignment across a multi-technology environment.

This is a strong fit for someone with a solid engineering foundation who has had exposure to system design or architecture and is looking to continue building in that area.
Responsibilities

Support system integration across network, hardware, and software environments

Assist in developing and maintaining system design documentation and diagrams

Work with senior engineers to evaluate and implement technical solutions

Support system upgrades, enhancements, and overall environment stability

Ensure systems align with operational and interoperability requirements

Analyze workflows and assist in identifying areas for improvement

Support compliance with security and DoD standards

Required Qualifications

Active Secret clearance

IAT Level II certification (Security+ or equivalent)

3-5+ years of experience in systems, network, or infrastructure engineering

Experience supporting DoD or federal IT environments

Exposure to system integration, documentation, or design efforts

Strong understanding of enterprise IT environments

Preferred Qualifications

Experience supporting design discussions or architecture efforts

Familiarity with OSI model or system interoperability concepts

Exposure to security practices or system hardening

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Thu, 30 Apr 2026 00:00:00 EDT 0 <![CDATA[System Administrator]]> Location: Ashburn, VA Onsite 3 days a week
Employment Type: Full-Time

Summary

A Global Media and Technology company is seeking a System Administrator to join their team in Ashburn, VA.

This multifaceted role combines systems engineering, systems administration, and performance testing to design, deploy, and optimize large-scale virtualized and distributed platforms, including VPIM, and VCEM.

The ideal candidate is an experienced engineer with strong expertise in Linux system administration and Kubernetes

Key Responsibilities

Systems Engineering & Administration

Configure, monitor, and maintain complex Linux-based platforms and infrastructure.

Design, deploy, and support distributed architectures in Kubernetes, Docker, and Red Hat environments

Manage and optimize infrastructure including Cisco switches, F5 load balancers

Develop, document, and maintain Methods of Procedure (MOPs) and system configuration standards.

Performance & Integration- Device Testing

Perform performance, functional, regression, scalability, and security testing for each release for environments a devices

Develop automated test frameworks using Python, Ansible, and Terraform.

Validate DHCP, DNS, IPsec, IPv4/IPv6, and address management features.

Execute system integration testing across VPIM, VCEM, and Eview platforms to ensure stability and interoperability.

Utilize Wireshark, Ixia IxLoad, Spirent, and CDrouter for packet-level network analysis and load testing.

Create detailed test plans, scripts, and validation reports to support release readiness.

Conduct root cause analysis on failed test cases and collaborate with engineering teams to resolve issues.

Automation & DevOps

Automate system deployment, testing, and monitoring using Python, Ansible, and Terraform.

Integrate automation pipelines within Jenkins or similar CI/CD environments.

Maintain lab automation frameworks for rapid provisioning and teardown of test environments.

Operations & Support

Support production and staging environments, providing expert-level troubleshooting.

Coordinate with development, QA, and operations teams to ensure system uptime and reliability.

Maintain detailed system documentation and architecture diagrams in Confluence.

Qualifications

Bachelor s degree in Computer Science, Engineering, or related field (or equivalent experience).

5+ years of experience in systems engineering, systems administration, or performance testing.

Expertise in Linux server administration, configuration, monitoring, and troubleshooting.

Proficiency in Python (preferred coding language) and Linux shell scripting.

Hands-on experience with Kubernetes, Docker, Cisco networking, and F5 load balancers.

Strong understanding of DHCP, DNS, IPsec, IPv6, and network troubleshooting.

Experience in load, performance, and regression testing of distributed or virtualized systems.

Familiarity with Wireshark, Ixia IxLoad, Spirent, CDrouter, or other performance analysis tools.

Experience with CI/CD, Jenkins, Ansible, Terraform, and Jira.

Excellent written and verbal communication skills with strong documentation discipline.

Preferred Certifications / Nice-to-Haves

Linux System Administration (RHCSA/RHCE) or equivalent certification.

Cisco (CCNA, CCNP/CCIE), Juniper (JNCIA, JNCIP/JNCIE), or Arista Certified Engineering (ACE) certifications.

Certifications in Network Virtualization or Automation

Experience with secure coding, vulnerability scanning, and automated monitoring.

Demonstrated expertise in automated test development, network performance analysis, and reliability engineering.

]]> Wed, 15 Apr 2026 00:00:00 EDT 0 <![CDATA[Quality Assurance Auditor]]> We are seeking an experienced and knowledgeable Quality Assurance (QA) Auditor to support our cGMP Supplier Quality operations and external audit program, as needed.
Reporting to the Vice President of Quality, the QA Auditor will support the execution of Suppler Quality Management (SQM) and Audit Programs for late-stage clinical operations. This role will ensure supplier qualifications and external audits are performed in a timely manner to meet quality and business objectives.
The ideal candidate will have three to five years of supplier quality experience in GMP-regulated environments, with demonstrated expertise in supplier qualification, audit execution, and quality oversight.

Key Responsibilities

Collaborate with QA leadership to enhance and maintain procedures related to the selection, qualification and ongoing management of GMP suppliers, as well as the execution of the external audit program.

Maintain GMP vendor files and the Approved Supplier List (ASL), and perform periodic assessment to ensure all vendor certifications, licenses, and required documentation remain current and compliant.

Support the drafting, review, and maintenance of Quality Technical Agreements, as required.

Apply auditing expertise to support the supplier and external audit schedule, including developing audit plans and conducting routine quality audits of GMP suppliers and service providers.

Maintain accurate and up-to-date audit reports, audit responses, and associated corrective and preventive actions (CAPAs).

Conduct follow-ups on supplier audit corrective actions to ensure timely and effective closure.

Support the QA Operations team in the investigation of product quality complaints, quality events, incidents and CAPAs related to materials or supplier-provided services.

Write, revise, and review Standard Operating Procedures (SOPs) and other GMP documentation in support of continuous improvement initiatives to enhance Supplier Quality efficiency and compliance.

Qualifications, Experience & Competencies

Bachelor s degree in a Life Sciences discipline preferred.
Minimum of three (3) years of Supplier Quality experience working within a cGMP-regulated Quality Assurance environment;cell therapy experience preferred
Current auditor certification (i.E., ASQ Certified Quality Auditor) strongly preferred
Demonstrated knowledge and practical application of GMP principles, including 21 CFR parts 210 and 211, as they relate to supplier quality oversight.
Ability to work independently with minimal supervision while managing multiple priorities effectively.
Strong interpersonal and collaboration skills, with a demonstrated ability to work in a team-based environment.
Ability to apply a risk-based approach to supplier qualification, auditing, and quality decision-making.
Willingness and ability to travel up to one week per month to support on-site supplier and external audits.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Thu, 02 Apr 2026 00:00:00 EDT 0 <![CDATA[NetOps Lead Mid]]> Network Operations Lead (NOC) DoD Environment | Cisco | Cherry Point, NC
We are seeking a hands-on Network Operations Lead to support a high-impact DoD environment in Cherry Point, NC.

This is a technical leadership role within a 24/7 NOC. You will serve as the escalation point for complex network issues, guide operations staff, and help maintain stability across enterprise WAN/LAN infrastructure. This position requires someone who leads from the front staying hands-on while driving performance and accountability across the team.

Responsibilities

Lead daily operations within a mission-critical NOC environment

Act as the primary escalation point for routing, switching, and network outages

Support and mentor network operations staff while remaining technically engaged

Drive incident management, change management, and root cause analysis

Develop and refine SOPs, processes, and operational standards

Support network architecture, topology planning, and technology refresh initiatives

Ensure compliance with DoD security policies, STIGs, and cybersecurity requirements

Analyze monitoring tools and logs to proactively identify and resolve issues

Collaborate with engineers, administrators, and stakeholders on integrated solutions

Produce clear documentation, reporting, and operational updates

Qualifications

Strong hands-on experience with Cisco routing and switching

Experience with BGP, OSPF, VLANs, ACLs, and WAN/LAN troubleshooting

Background in a NOC or network operations environment (Tier 2 or higher)

Ability to manage escalations in a 24/7 operational setting

Experience with network monitoring tools, ticketing systems, and incident response

Strong communication skills with the ability to translate technical issues to leadership

Requirements

5+ years of network operations or engineering experience

DoD 8570 compliance:

Security+ (IAT Level II) required

IAT Level III preferred depending on environment

Cisco certification:

CCNA required

CCNP preferred

High School Diploma or GED (higher education is a plus)

(Active Secret Clearance or greater is a MUST have)
Preferred Experience

Experience supporting DoD or cleared environments

Familiarity with Cisco Catalyst (9000 series), DNA Center

Experience with ServiceNow or similar platforms

Background supporting enterprise or government-scale networks

Why This Role

Combination of leadership responsibility and hands-on technical work

Direct impact on mission-critical network operations

Opportunity to influence processes and operational standards

High-visibility role with long-term growth potential

Fit
This role is best suited for someone who is already acting as an escalation point within their team, is comfortable owning issues end-to-end, and can lead others without stepping away from the technical work.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Thu, 26 Mar 2026 00:00:00 EDT 0 <![CDATA[Software Engineering DBA Consultant]]> Full-stack developers will be required to see out a project from conception to the final product, requiring good organizational skills and attention to detail. Full Stack Developer Responsibilities:

Developing front end website architecture.

Designing user interactions on web pages.

Developing back-end website applications.

Creating servers and databases for functionality.

Ensuring cross-platform optimization for mobile phones.

Ensuring responsiveness of applications.

Working alongside graphic designers for web design features.

Seeing through a project from conception to finished product.

Designing and developing APIs.

Meeting both technical and consumer needs.

Staying abreast of developments in web applications and programming languages.

Full Stack Developer Requirements:

Degree in computer science.

Strong organizational and project management skills.

Proficiency with fundamental front-end languages such as HTML, CSS, and JavaScript.

Familiarity with JavaScript frameworks such as Angular JS, React, and Amber.

Proficiency with server-side languages such as Python, Java, PHP, and .Net.

Familiarity with database technology such as MySQL, Oracle, and MongoDB.

Excellent verbal communication skills.

Good problem-solving skills.

Attention to detail.

DBA Requirements:

Proficiency in MySQL/MariaDB database installation, management and production support.

Experience with Database monitoring and troubleshooting.

Experience in data modeling, database logical and physical design.

Understanding of MySQL/MariaDB underlying storage engines.

Understanding of MySQL/MariaDB partitioning.

Ability to plan resource requirements from high-level specifications.

Proficient analyzing and optimizing SQL statements.

Understanding of Sharding, Master-Master, Master-Slave replication.

Experience with MySQL/MariaDB containers for Docker/Kubernetes.

Experience with Data migrations, Export/Imports.

Shell scripting proficiency.

Linux/Unix proficiency.

Knowledge of MySQL/MariaDB features, such as its event scheduler, functions, stored procedures, triggers, etc.

Knowledge of standards and best practices in MySQL/MariaDB.

Additional Required Experience:

Home App
Mobile App
VPIM
VCEM

Location: Onsite 3 days a week in Ashburn, VA or Dallas, TX

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Tue, 24 Mar 2026 00:00:00 EDT 0 <![CDATA[Director, Biostatistics]]>
Job Summary:
We are seeking an experienced Director of Biostatistics to provide scientific and technical leadership for our clinical development programs. In this role, you will lead all biostatistical activities and serve as a biostatistical expert across all assigned projects, ensuring the highest standards of scientific rigor and regulatory compliance.
Key Responsibilities:
Provide statistical leadership and support across all clinical development functions and lead all assigned projects within the Biometrics department.
Participate and interact with clinical and cross-functional teams in the development of protocols, study design, and endpoints discussions.
Develop and review statistical sections of protocols, SAPs, study reports, and regulatory documents.
Apply advanced statistical methodologies, such as survival analysis, Bayesian analysis, handling missing data and adaptive designs.
Provide statistical support to Clinical Operations, Regulatory Affairs, Medical Affairs, Translational science, and RWE functions.
Support regulatory submissions work and generation of ISS/Client.
Ensure consistency within Biometrics functions, including Programming and Data Management, for all deliverables to enhance efficiency and quality.
Represent Biostatistics in meetings with regulatory authorities.
Develop and implement departmental SOPs for statistical activities in accordance with ICH, GCP, guidelines, and CDISC standards (SDTM/ADaM).
Manage and oversee the work of CROs and other external vendors to ensure the quality and timeliness of deliverables.
Qualifications, Experience, & Competencies:
A master s or PhD degree in biostatistics or a related field is required.
At least 10 years of experience in the pharmaceutical, biotechnology, or contract research organization (CRO) industry is essential.
Proficiency in SAS and/or R. Familiarity with CDISC standards (SDTM, ADaM) is essential.
Page 2 of 2
In-depth experience and expertise in applying biostatistical methodologies to clinical development are highly desirable.
Understanding of FDA, EMA and ICH regulations and guidelines. Experience working on regulatory submissions is preferred.
Excellent verbal and written communication skills are essential, along with the ability to work effectively as part of a team.
Must be able to work independently with minimal supervision.
Additionally, the ability to travel up to 5% of the time, depending on the business s needs, is required.

]]> Fri, 13 Mar 2026 00:00:00 EDT 0 <![CDATA[NOC T2 Network-Tech Lead]]> NOC T2 Network-Tech Lead :

Your primary responsibility is to provide Change Management and escalated Incident Management functions to GNOSC (Government Network Operations and Security Center) customers in a 24x7 environment. You will be part of a team that will support a Tier 1-2 organization through incident handling, training, creation of documentation and working technical project. This position is the most senior level of the Operations Support Staff.

Requirements

· In depth networking troubleshooting knowledge
· Test and repair software/hardware/routing issues in the customer WAN/LAN environment
· Excellent working and troubleshooting knowledge of Routing Protocols and Multiple CPE vendors: Cisco, Juniper, Aruba, etc.

Minimum Qualifications:

In depth network troubleshooting experience on a Layer 2-3 network. 5 years+ of Tier 3 experience in a Network Operations Center as network engineer. Extensive Experience with network management tools and solving complex networking problems. Must have the ability to work in highly closed spaces.
SEC+, CCNA &/ or CCNP REQUIRED

( Active TS Clearance Required)

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Thu, 12 Mar 2026 00:00:00 EDT 0 <![CDATA[CNO Developer (iOS/Android/Harmony)]]>
CNO Developer - Android/Harmony and/or iOS
CNO Developer (Android and/or iOS focus)

TS/SCI clearance required (will provide upgrade to FS Poly!)

Description:

On the job you will support development activities across a wide range of technologies and functional areas;foster customer collaboration throughout the entire development life-cycle;aid with mission-critical work. The CNO Developer will be expected to work with the team in determining and developing innovative approaches to research problems

Basic Qualifications:

3+ years experience with Android or or Harmony or iOS operating systems

3+ years experience with C and Python

TS/SCI with the ability to get an FSP while on contract (it is not required to start)

Full time on site with sponsor in northern VA

Required Skills:

3+ years experience with Android or Harmony or iOS operating systems

3+ years experience with C and Python

TS/SCI with the ability to get an FSP while on contract (it is not required to start)

Full time on site with sponsor in northern VA

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Mon, 23 Feb 2026 00:00:00 EST 0 <![CDATA[Deployed Support Specialist Mid]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Mon, 02 Feb 2026 00:00:00 EST 0 <![CDATA[Testing Data Analyst]]>
Advanced analysis of network traffic TCP/UDP frames using analysis tools such as Wireshark, airpcap ng and more.

Troubleshooting Speed test related issues on gig bit speeds and higher on 10BaseT and NBaseT network configurations.

Configure, test and deploy applications on Linux Operating systems.

Develop, integrate, and test automation scripts for installation and deployment of the applications on Linux base OS.

Develop, integrate and troubleshoot third party applications on different Linux OS.

Troubleshoot any network/system/service related issues with involved testing teams.

Test server application for remote and client speed test application in Lab environment.

Test DNS, DHCP, static and dynamic address allocations with BHR devices.

Develop test plans and user stories for Performance testing of the BHRs.

Develop automated test scripts for performance testing of the BHRs in a singular and multi-node fashion.

Use statistical methods to analyze data and generate useful reports.

Use data to create models that depict trends based on the devices/user generated data programmatically.

Working with HDFS, Spark, Hive and Hue to collect and represent data.

Knowledge of R, Python, RappidMinner and other programming languages for data analysis and visualization.

Advance understanding of data normalization and representation.

Understanding of computer architecture, networking and communication tools such as Broadband Home Routers, Set-Top boxes and WiFi AP/extenders.

Youâll need to have:

Bachelorâs degree or 5 or more years of experience in Linux administration.

Proven experience with In Home architecture including Wi-Fi technologies and performance measurements.

Ability to work with Linux-friendly applications and able to troubleshoot it when issue arise.

Able to script in shell as well as Python, Perl or ruby.

Basic Networking Knowledge.

Know how to setup, configure and use complex Linux servers and Linux base applications.

Extensive experience of working on Linux/Unix systems.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Wed, 28 Jan 2026 00:00:00 EST 0 <![CDATA[Communications Network Engineer]]> Evaluate communication hardware and software, as well as troubleshoot Local Area Networks/Base Area Networks/Wide Area Networks (LAN/BAN/WAN), and other network related problems. Administer LAN/BAN/WANs. Schedule conversions and cutovers. Coordinate with all responsible users and sites. Specialized experience in the performance and configuration of networks as well as the integration and testing of complex large-scale computer integrated networks. Must possess an Original Equipment Manufacturer (OEM) network support certification such as a Cisco Certified Network Associate (CCNA).

Required:
Sec+ (Day 1)
CCNA (w/ in 6 months of being hired)
Active DOD Secret Clearance Required
Active ability to work in closed spaces.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Wed, 07 Jan 2026 00:00:00 EST 0 <![CDATA[Virtual Server Administrator Mid]]> Virtual Server Administrator Mid-Level
Location: Quantico, VA
Clearance Required: Active DoD Secret Clearance
Education: High School Diploma or equivalent
Experience: 5+ years of IT systems administration
Certifications Required:
VMware Certified Associate (VCA) required at start
VMware Certified Professional (VCP) must be obtained within 6 months
IAT Level II (e.G., Security+ CE, SSCP, GSEC) must be valid for 3+ years
Your Mission:
As a Virtual Server Administrator, you ll support the integrity and performance of a secure, virtualized Microsoft server environment critical to national defense. You ll perform hands-on administration, patching, monitoring, and issue resolution in a fast-paced DoD environment at Quantico. This role is ideal for a cleared IT professional with VMware experience looking to deepen their skillset in a mission-driven setting.
What You ll Do:
Manage and maintain Microsoft-based virtual server environments
Perform daily system health checks, apply patches, and maintain uptime
Troubleshoot and resolve infrastructure issues (VMware, AD, DNS, DHCP)
Work with cross-functional teams and government reps to resolve incidents
Utilize remote server management tools and follow change control procedures
Maintain accurate system documentation and compliance with DoD standards
What You Bring:
5+ years of hands-on IT systems administration experience
Strong knowledge of Active Directory, DNS, DHCP, and virtualization
Working experience with VMware (vSphere, vCenter) and clustering
Ability to manage patching, system audits, and infrastructure troubleshooting
A collaborative mindset and strong communication skills
Active DoD Secret Clearance and required certifications
Why You ll Want This Role:
Work in a secure, high-impact DoD environment at Quantico
Gain experience managing enterprise virtualization tools in a production environment
Be part of a mission-focused team supporting national security
Opportunity to grow toward senior-level virtualization or cybersecurity roles

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Fri, 01 Aug 2025 00:00:00 EDT 0 <![CDATA[Network Enterprise Management Design Engineer Senior]]> We re seeking an experienced Network Enterprise Management Design Engineer Senior to support daily engineering operations for a mission-critical Department of the Navy (DON) program at Camp Pendleton. This is a highly technical role supporting NetOps visibility, infrastructure control, and cybersecurity across Navy/Marine Corps enterprise environments.

Key Responsibilities:

Support and assist the Government Lead with daily systems engineering operations.

Evaluate and troubleshoot LAN, BAN, and WAN communication hardware and software.

Provide technical leadership on large-scale system integration and testing.

Design solutions for full-spectrum, near real-time IT service monitoring and vulnerability analysis.

Enable Navy/Marine Corps NetOps through network management systems and C2 facilities.

Facilitate operational control over network services and infrastructure for DON.

Install and integrate server systems, perform schema extensions for directory services.

Support disaster recovery, security patching, and integration with Host-Based Security System (HBSS).

Implement Active Directory (AD), LDAP, and PKI for two-factor authentication and access control.

Conduct network analysis and deep packet inspection (Wireshark, Sniffer, etc.).

Build and manage system dashboards and status monitoring tools.

Install, configure, and maintain NetScout systems (nGenius One, Performance Manager, Infinistream).

Design and support RedHat Enterprise Linux solutions and Rights Management for users and admins.

Operate and manage a range of systems including Cisco, Juniper, Fortinet, Brocade, McAfee, Client OMi/NNMi, Client Server/Network Automation, and more.

Ensure compliance with IA and Comply-to-Connect standards.

Required Qualifications:

Active SECRET clearance

ITIL v3 Foundation Certification (mandatory)

5+ years of experience with:

Network engineering (LAN/WAN, routing, protocols)

Directory services (Active Directory, LDAP)

Security tools (PKI, two-factor authentication, HBSS)

Packet analysis tools (Wireshark, Sniffer)

NetScout system setup and support

RedHat Enterprise Linux platforms

Enterprise consoles (Cisco, Fortinet, Juniper, McAfee, Client suite)

Familiarity with DoD IT infrastructure and compliance standards

Preferred:

Experience in Navy/Marine Corps environments

Knowledge of Comply to Connect and DoN network policies

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 09 Jun 2025 00:00:00 EDT 0 <![CDATA[Communications Network Engineer Senior]]> Evaluate communication hardware and software, as well as troubleshoot Local Area Networks/Base Area Networks/Wide Area Networks (LAN/BAN/WAN), and other network related problems. Administer LAN/BAN/WANs. Schedule conversions and cutovers. Coordinate with all responsible users and sites. Specialized experience in the performance and configuration of networks as well as the integration and test of complex large-scale computer integrated networks. Must possess an Original Equipment Manufacturer (OEM) network support certification such as a Cisco Certified Network Associate (CCNA).

Required:
Sec+ (Day 1)
CCNA (w/ in 6 months of being hired)
Active DOD Secret Clearance
Bachelors Degree

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Tue, 18 Mar 2025 00:00:00 EDT 0 <![CDATA[Cyber Security Specialist Mid]]> Cybersecurity Specialist Mid Quantico, VA (MCCOG)

Position Overview:
We are seeking a skilled Cybersecurity Specialist Mid to oversee and enhance the security of Information Systems (IS) in a high-impact DoD environment. The role involves ensuring data availability, integrity, authentication, confidentiality, and non-repudiation while implementing and maintaining robust security measures across communication systems and networks.
Key Responsibilities:

Information Security & Compliance:

Implement and monitor security controls to align with governmental security standards.

Develop and enforce approved security policies, plans, and procedures.

Ensure compliance with DoD security frameworks and industry best practices.

Network & Cyber Defense:

Operate and maintain firewalls, IDS/IPS, VPNs, and endpoint security solutions to safeguard networks.

Utilize Host-Based Security Systems (HBSS) and Intrusion Detection & Prevention Systems (IDS/IPS) to detect and mitigate threats.

Conduct network security monitoring, forensics, and incident handling.

Perform certification and accreditation of IS and networks.

Cybersecurity Incident Response:

Identify and analyze cybersecurity incidents using tools such as Tenable SecurityCenter, RedSeal, McAfee SIEM, and Imperva Web Application & Database Firewalls.

Perform forensic investigations and execute remedial actions.

Maintain and report cyber defense operational metrics.

Continuity & Key Management:

Support Continuity of Operations Plan (COOP) / Disaster Recovery (DR) strategies.

Operate and manage Electronic Key Management Systems (EKMS) and Public Key Infrastructure (PKI).

Desired Tool Experience:

Security & Compliance: HBSS, Tenable SecurityCenter, RedSeal, McAfee SIEM, PKI, IPS

Defensive Cyber Operations: Imperva Web Application & Database Firewalls

Requirements:

Education: High school diploma required

Clearance: Active DoD Secret Clearance required

Certification: Security+ (CompTIA) or higher required

Location: Quantico, VA

This is a highly technical and mission-critical role, ideal for professionals looking to apply their cybersecurity expertise in a dynamic Department of Defense (DoD) environment. If you meet the requirements and are ready for a challenge, apply today!

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Wed, 29 Jan 2025 00:00:00 EST 0 <![CDATA[NETWORK ROUTING DESIGN ENGINEER SENIOR]]> Position Overview
We are seeking an experienced Network Routing Design Engineer Senior to join our team in support of our DOD/Government Client. The ideal candidate will design, implement, and optimize complex routing solutions to ensure high performance, reliability, and scalability of our network infrastructure. This role requires advanced technical expertise in routing protocols, hands-on problem-solving, and a collaborative mindset to drive strategic initiatives.
Key Responsibilities

Design and Implementation : Develop and deploy advanced routing architectures utilizing protocols such as BGP, OSPF, EIGRP, and MPLS to support business operations and growth.

Optimization and Troubleshooting : Analyze and enhance network routing for performance, scalability, and redundancy. Diagnose and resolve complex routing and connectivity issues in a timely manner.

Automation and Innovation : Leverage automation tools (Python, Ansible, Terraform) to streamline routing configurations and improve efficiency. Stay updated on emerging technologies to integrate innovative solutions.

Documentation and Reporting : Maintain accurate and up-to-date network diagrams, configurations, and technical documentation. Generate performance reports and provide strategic insights to leadership.

Collaboration and Leadership : Partner with cross-functional teams to align network design with organizational goals. Mentor and guide junior engineers to elevate team capabilities.

Qualifications

Education : Bachelor s degree in Computer Science, Information Technology, or a related field (Master s degree preferred).

Experience : Minimum 7+ years in network engineering, with substantial expertise in routing and network design for enterprise or service provider environments. (10+ preferred)

Required Skills

Advanced knowledge of routing protocols: BGP, OSPF, EIGRP, and MPLS.

Experience with WAN, SD-WAN, and MPLS technologies.

Proficiency in network monitoring and analysis tools (e.G., SolarWinds, Cisco Prime, NetFlow).

Familiarity with network security principles and best practices.

Scripting and automation skills with tools like Python, Ansible, or Terraform (preferred).

Certifications such as CCNP, CCIE, or JNCIE (highly preferred).

Strong communication, documentation, and problem-solving abilities.

Active DOD Secret Clearance

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Thu, 02 Jan 2025 00:00:00 EST 0 <![CDATA[Enterprise Service Desk Specialist Senior]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Mon, 22 Apr 2024 00:00:00 EDT 0 <![CDATA[Deployed Support Specialist Mid]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Tue, 20 Feb 2024 00:00:00 EST 0 <![CDATA[IT Specialist Senior]]> Perform advanced systems installation, operation, integration, and troubleshooting in order to maintain optimum Information Technology (IT) system operations. Design and oversee upgrades and new installs of IT systems and services ensuring coordination with Cyber Security Specialist. Perform Tier III upgrades of networking systems, IT systems, and storage networking. Perform Tier III troubleshooting, optimization, and performance management of Internet Protocol (IP), Domain Name System (DNS), Dynamic Host Configuration Protocol (DHCP), and routing protocols. Integrate enterprise, regional, and local IT systems ensuring current network operations are sustained or oversee their recovery. Ten plus (10+) years of IT experience including Internet Protocol version 6 (IPv6), Enhanced Interior Gateway Routing Protocol (EIGRP), Border Gateway Protocol (BGP), Virtual Local Area Networks (VLANs), Virtual Private Networks (VPNs), and Network Address Translation (NAT). Must possess a Cisco Certified Network Professional (CCNP), Cisco Certified Design Professional (CCDP), Microsoft Technology Associate (MTA), Microsoft Certified Solutions Associate (MCSA) or a Microsoft Certified Technology Specialist (MCTS) certification.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Tue, 30 Jan 2024 00:00:00 EST 0 <![CDATA[Full Stack Engineer ( Mid level)]]> Our Customer is on a mission to develop products and services for our customers around the world to maximize their data. We believe enabling data starts with foundational data strategy, data architecture, data science and engineering and the practice and discipline to scale and to drive meaningful customer and business impact.

Full-Stack Engineer (Mid-Level)
Are you a passionate full-stack engineer seeking an opportunity to contribute to cutting-edge applications and make a real impact? Do you possess a deep understanding of both front-end and back-end technologies, and thrive in collaborative environments?

As a full-stack engineer, you'll play a pivotal role in the development and deployment of our next-generation web applications. You'll leverage your expertise in front-end technologies like HTML, CSS, JavaScript, and React to craft intuitive and user-centric interfaces. On the back-end, you'll utilize your knowledge of Python, Node.Js, and Express to build robust and scalable systems that ensure seamless application performance.

This role offers more than just technical challenges;it's an opportunity to:
Shape the future: Be at the forefront of innovation, designing and developing applications that push the boundaries of our industry.
Collaborate with the best: Join a team of talented and passionate engineers who are dedicated to achieving excellence together.
Make a real difference: Contribute to products that positively impact the lives of our users, leaving a lasting legacy.
Thrive in a stimulating environment: Enjoy a culture of continuous learning, open communication, and professional growth opportunities.

To excel in this role, you should possess:
3+ years of experience as a full-stack engineer
Bachelor's Degree in Computer Science or related field
Proficient in front-end technologies (i.E. HTML, CSS, JavaScript, React, NodeJS, Angular, Express)
Strong understanding of back-end technologies (i.E.Python, Java, Go)
Familiarity with databases (i.E. MySQL, MongoDB)
Practical experience working in Cloud environments (i.E. AWS or GCP)
A passion for building high-quality, user-friendly applications
Excellent problem-solving and debugging skills
The ability to work effectively both independently and as part of a team
A positive attitude and a strong desire to learn and grow

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.]]> Fri, 26 Jan 2024 00:00:00 EST 0 <![CDATA[Senior Software Developer]]>
**Senior Software Engineer Opportunity**
We're seeking a Senior Software Engineer with 10-15 years of experience, ready for a leadership role. The ideal candidate will have an extensive understanding of the software development lifecycle, from design to architecture. This role is perfect for those passionate about innovation, collaboration, and creating high-impact solutions.

As a Senior Software Engineer, you will significantly influence our software direction. Your responsibilities include designing, developing, and implementing complex systems and features, as well as mentoring junior engineers. This role is not just technically challenging;it offers the chance to lead technology initiatives, mentor technically, make a real-world impact, and foster a culture of excellence and continuous learning.

**Key Qualifications:**
- 10-15 years in software engineering
- Bachelor's in Computer Science or similar
- Proficiency in multiple programming languages and technologies
- Expertise in at least one language (e.G., Python, C++, Java)
- Strong experience with SQL, NoSQL (e.G., MySQL, MongoDB)
- Experience in front-end technologies (HTML, CSS, JavaScript, React)
- Familiarity with Client, data environments, and cloud platforms (AWS, GCP)
- Knowledge of container orchestration (Kubernetes, Docker) and automation stacks (Terraform)
- Proven capability in software system design and implementation
- Exceptional problem-solving and analytical skills
- Excellent communication and leadership abilities.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Fri, 26 Jan 2024 00:00:00 EST 0 <![CDATA[Communications Network Engineer]]> Evaluate communication hardware and software, as well as troubleshoot Local Area Networks/Base Area Networks/Wide Area Networks (LAN/BAN/WAN), and other network related problems. Administer LAN/BAN/WANs. Schedule conversions and cutovers. Coordinate with all responsible users and sites. Specialized experience in the performance and configuration of networks as well as the integration and testing of complex large-scale computer integrated networks. Must possess an Original Equipment Manufacturer (OEM) network support certification such as a Cisco Certified Network Associate (CCNA).

Required:
Sec+ (Day 1)
CCNA (w/ in 6 months of being hired)
Active ability to work in closed spaces.

Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.]]> Tue, 26 Dec 2023 00:00:00 EST 0 <![CDATA[NetOps Specialist Senior]]>
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
]]> Wed, 15 Nov 2023 00:00:00 EST 0