Scientist – Cell Biology & Potency

Eurofins•Berkeley, CA

2d•$60,000 - $80,000

About The Position

Supports late-stage cell therapy products through analytical assay development, assay qualification and validation, and sample testing. Contributes to the design, planning, execution, and optimization of analytical assay development activities and 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, and provides proactive 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 and maintenance, and general laboratory compliance. The role is based in a laboratory environment and is listed as Monday through Friday, first shift, with no weekend or holiday work. Candidates within a commutable distance of Berkeley, California, are encouraged to apply. The stated compensation range is $60,000–$80,000 yearly.

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.

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 analytical assay development activities and assay 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 status updates on assigned activities, risks, and timelines to project teams and management.
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 and maintenance, and general laboratory compliance.