Lead the analytical lifecycle for cell therapy products, setting strategy, standards, and governance across global testing networks.
Locations (3)
Gaithersburg, Maryland, United States
Rockville, Maryland, United States
Tarzana, California, United States
Compensation
The annual base pay for this position ranges from $138,393 to $207,589. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Responsibilities
Define and govern analytical lifecycle strategy and network-level governance standards
Lead method transfer, validation, comparability, and bridging activities
Oversee network method-performance monitoring and risk assessment
Provide analytical lifecycle content and technical review for regulatory submissions and inspections
Drive continuous improvement and harmonization of global analytical lifecycle processes
Requirements
Bachelor's in analytical sciences, biotechnology, biochemistry, cell or molecular biology, pharmaceutical sciences, engineering, or a related discipline
Master's in analytical sciences, biotechnology, biochemistry, cell or molecular biology, pharmaceutical sciences, engineering, or a related discipline
PhD in analytical sciences, biotechnology, biochemistry, cell or molecular biology, pharmaceutical sciences, engineering, or a related discipline
Nice to have: CAR-T
Nice to have: autologous or allogeneic cell therapy
Analyze market data and trends to identify opportunities for revenue growth, evaluate pricing strategies, enhance forecasting, prepare reports, and support the Director of Revenue Management in developing data-driven pricing strategies.
Responsibilities
Analyze market data and trends to identify opportunities for revenue growth
Evaluate pricing strategies and provide insights to optimize revenue management
Enhance forecasting capabilities to align with market conditions and consumer preferences
Prepare detailed reports and presentations on revenue performance and market insights
Support Director of Revenue Management to collaborate with the sales and marketing teams to develop data-driven pricing strategies
Requirements
Bachelor’s degree in Business, Economics, Hospitality Management, or a related field
Provide hands-on quality engineering support focusing on continuous improvement for injection molding and assembly, from new-product introduction and process validation through ongoing production.
Responsibilities
Drive continuous improvement projects to enhance quality and efficiency
Analyze data, identify trends, and perform root cause investigations
Implement and verify corrective and preventive actions (CAPA)
Partner with cross-functional teams to optimize processes and reduce waste
Support Lean Six Sigma initiatives and quality objectives
Requirements
Bachelor’s degree in engineering or technical discipline, or equivalent education and experience
Drive product and test development from pre‑silicon to mass production, including test hardware and software development, characterization plan development, and design IP characterization.
Responsibilities
Drive product and test development from pre‑silicon to mass production
Lead first silicon debug, process experiment definition, multiple‑source fab matching, and guard band / test limit generation
Drive short‑term and long‑term test time reduction (TTR) and yield improvement initiatives
Leverage AI‑assisted data analytics and machine learning tools to accelerate yield variance control
Manage multiple projects in parallel, balancing NPI milestones and sustaining commitments
Requirements
Bachelor's degree in Electrical and Electronics Engineering
Nice to have: prior lab or internship experience
Nice to have: familiarity with AI‑assisted engineering platforms or LLM‑based tools
Oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff.
Compensation
Salary Range $64,300.00 - $99,700.00 / Annually
Responsibilities
Acts as the primary liaison to PI in developing plans for research projects and discussing the interpretation of results
Collaborates in the preparation of manuscripts for publication and preparation of grant proposals to sponsoring agencies
Assists in the preparation of amendments to protocols and/or modifications to study design as appropriate
Serves as responsible for the development of forms, questionnaires and the application of research techniques
Assists in writing instructional procedure manuals for study progress, data collection and coding
Supports clinical research activities within the Memory Diagnostic Center, focusing on participant-facing tasks, data entry, and protocol compliance.
Compensation
$54,600.00 - $81,900.00 / Annually
Responsibilities
Coordinates clinical research activities, including study startup, participant visits, clinical assessments, phlebotomy, biospecimen collection, and other protocol-specific procedures.
Collaborates with study investigators, physicians, and research staff to ensure adherence to approved protocols and institutional requirements.
Assists in developing plans for research projects and discusses the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies.
Assists in writing instructional procedure manuals for study progress, data collection, and coding.
Reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
Requirements
Bachelor’s degree or combination of education and/or experience may substitute for minimum education
Provide senior-level bench expertise and scientific leadership in genetic and translational research at NIH.
Compensation
The annual salary range for this position is $98,000.00-$163,000.00.
Responsibilities
Investigate genetic modifiers and biological mechanisms influencing disease severity and clinical outcomes.
Apply cellular biology, molecular biology, immunology, and bioinformatics methods to study red blood cell dysfunction, acute pain, and inflammation.
Identify and evaluate biomarkers for monitoring disease processes and treatment response.
Conduct preclinical studies using animal models, primarily mice, to assess disease mechanisms and investigational therapies.
Integrate genotype–phenotype analyses with clinical, laboratory, imaging, and diagnostic data to characterize disease manifestations and identify therapeutic targets.
Requirements
PhD or MD in human genetics, molecular biology, biochemistry, immunology or closely related field
Nice to have: strong written and verbal communication
Quality Engineer responsible for root‑cause investigations, CAPA, process controls, and quality assurance across manufacturing, supplier, and customer sites.
Responsibilities
Lead investigations into internal non‑conformances, warranty claims, and customer quality escapes using structured methodologies (8D, 5‑Why, Fishbone).
Develop and maintain PFMEAs, Control Plans, and Standard Operating Procedures; conduct process capability studies and support SPC rollout.
Monitor supplier performance scorecards, execute audits, and manage supplier corrective actions to ensure incoming component integrity.
Support site adherence to ISO 9001 standards, participate in MRB/NCR dispositions, and support internal and customer audits.
Drive measurable scrap and rework reductions across production lines while guiding and mentoring plant quality inspectors and technicians.
Requirements
Bachelor’s degree in Mechanical, Manufacturing, Industrial Engineering, Quality, or a related technical discipline.
Nice to have: Certified Quality Engineer (ASQ CQE)
Nice to have: Certified Quality Auditor (ASQ CQA)
Nice to have: Lean Six Sigma Green Belt/Black Belt
Provide support on biomarker studies to meet the company's goals, objectives and quality standards.
Compensation
The North Carolina salary range for this position is: $27-$31.50 per hour
Responsibilities
Responsible for cell experiments in vitro, pre‑treatment and processing of tissue samples, and execution of a variety of experiments including flow cytometry, pathology/IHC, proteomics, hematology
Carry out work in strict accordance to SOPs and training sessions
Carefully record the experimental process and data and submit timely reports to supervisors
Analyze, summarize, and report experimental data and relevant documents to supervisors
Effective communication within the global biomarker team and with other departments
Requirements
B.S. or above in biotechnology, cell biology, immunology, oncology or other related disciplines
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