Scientist – Molecular Biology
About The Position
Supports late-stage cell therapy products through analytical assay development, assay qualification and validation, and sample testing. The role contributes to the design, planning, execution, and optimization of analytical assay development and validation studies. It involves conducting 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; provides status updates on activities, risks, and timelines; and supports the preparation and review of assay-related documentation, including protocols, methods, and reports. The role collaborates with cross-functional teams on analytical strategy and project execution, and contributes to laboratory operations such as ordering, organization, equipment monitoring and maintenance, and general laboratory compliance.
Requirements
- Bachelor’s degree in Biology, Chemistry, or a related scientific discipline.
- 4+ years of relevant industry experience.
- 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.
- 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 QX ONE, QX 200, and QuantStudio 7 instrumentation.
- Additional experience in analytical development or GMP assay validation.
- Experience supporting late-stage development or regulated laboratory environments.
- Location within a commutable distance to Berkeley, CA is highly encouraged.
Responsibilities
- Support late-stage cell therapy products through analytical assay development, assay qualification/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 proactive 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.
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
