Scientist – Cell Biology & Potency
About The Position
Eurofins PSS is seeking a Scientist to support late-stage cell therapy products through analytical assay development, assay qualification and validation, and sample testing. The role contributes to planning, executing, and optimizing assay development and validation studies; performing experiments; analyzing and interpreting data; troubleshooting technical issues; and communicating results and recommendations to internal stakeholders. The Scientist prepares and presents scientific data in technical reports, team discussions, and departmental meetings, and provides project teams and management with proactive updates on assigned activities, risks, and timelines. The position also supports preparation and review of assay-related technical documentation, collaborates with cross-functional teams on analytical strategy and project execution, and contributes to laboratory operations and compliance. The role is based at a client site in Berkeley, California. The schedule is Monday through Friday on first shift, with no weekend or holiday work. The compensation range is $60,000–$80,000.
Requirements
- Bachelor’s degree in Cell Biology or a related scientific discipline.
- At least 4 years of relevant industry experience.
- Strong experience with mammalian cell culture.
- Hands-on experience with cell biology analytical methods, including cell count and viability, high-resolution imaging, live-cell imaging, and cell-based potency assays.
- Working knowledge of analytical method development, assay optimization, qualification, and validation in a GMP environment.
- Ability to analyze complex experimental data, troubleshoot assay performance issues, and support method improvements.
- Strong oral and written communication skills, including the ability to write and review SOPs, technical reports, and scientific documentation.
- Ability to collaborate effectively with peers, managers, and cross-functional teams in a fast-paced, multidisciplinary environment.
- Solid understanding of GMP requirements and documentation practices.
- Authorization to work in the United States without current or future sponsorship requirements.
Nice To Haves
- Master’s degree.
- Experience with fluorescence microscopy, Incucyte, and Cytation instrumentation.
- Experience with HPLC.
- Additional experience in analytical development or GMP assay validation.
- Experience supporting late-stage development or regulated laboratory environments.
- Candidates within a commutable distance of Berkeley, California are highly encouraged to apply.
Responsibilities
- Support late-stage cell therapy products through analytical assay development, assay qualification and validation, and sample testing.
- Contribute to the design, planning, execution, and optimization of assay development activities and validation studies.
- Perform experiments, analyze and interpret data, troubleshoot technical issues, and communicate results and recommendations to internal stakeholders.
- Prepare and present scientific data in technical reports, team discussions, and departmental meetings.
- Provide project teams and management with clear, proactive updates on activities, risks, and timelines.
- Support preparation and review of assay-related technical documentation, including protocols, methods, and reports.
- Collaborate with cross-functional teams to support analytical strategy and timely project execution.
- Contribute to laboratory operations, including ordering, organization, equipment monitoring, maintenance, and general laboratory compliance.
Benefits
- Comprehensive medical coverage, with dental and vision options.
- Life and disability insurance.
- 401(k) with company match.
- Paid holidays and vacation.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
