Scientist – Molecular Biology
About The Position
Eurofins PSS works with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries, providing mission-critical testing. PSS is part of Eurofins Scientific, an international life sciences company with a vast network of laboratories and employees globally. Life at Eurofins is a meritocracy where individuals are empowered and rewarded for success, fostering rapid advancement and personal growth. This role supports late-stage cell therapy products through analytical assay development, assay qualification/validation, and sample testing. The position involves contributing to the design, planning, execution, and optimization of analytical assay development and validation studies. Responsibilities include performing experiments, analyzing and interpreting data, troubleshooting technical issues, and communicating results and recommendations to internal stakeholders. The role also requires preparing and presenting scientific data, providing clear status updates, and supporting the preparation of assay-related technical documentation. Collaboration with cross-functional teams is essential for analytical strategy and project execution, alongside contributing to laboratory operations.
Requirements
- Strong experience with mammalian cell culture.
- Hands-on experience with DNA/RNA extraction and molecular biology assays such as qPCR, ddPCR, and DNA/RNA quantitation.
- Working knowledge of analytical method development, assay optimization, qualification, and validation in a GMP environment.
- Demonstrated 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.
- Bachelor’s degree in Biology, Chemistry, or a related scientific discipline required.
- 4+ years of relevant industry experience.
Nice To Haves
- Experience with QX ONE, QX 200 and QuantStudio 7 instrumentation preferred.
- Master’s degree preferred.
- Additional experience in analytical development or GMP assay validation strongly preferred.
- Experience supporting late-stage development or regulated laboratory environments is preferred.
- Candidates located within a commutable distance to Berkeley, CA are highly encouraged to apply.
Responsibilities
- Supports late-stage cell therapy products through analytical assay development, assay qualification/validation, and sample testing activities.
- Contributes to the design, planning, execution, and optimization of analytical assay development activities and assay validation studies.
- Performs experiments, analyzes and interprets data, troubleshoots technical issues, and communicates results and recommendations to internal stakeholders.
- Prepares and presents scientific data in technical reports, team discussions, and departmental meetings.
- Provides clear and proactive status updates on assigned activities, risks, and timelines to project teams and management.
- Supports preparation and review of assay-related technical documentation, including protocols, methods, and reports.
- Collaborates with cross-functional teams to support analytical strategy and timely project execution.
- Contributes 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
