Live opening · Posted 7 hours ago
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About the role
Description supplied by the original job listing.
Research Associate responsibilities include, but are not limited to, the following:
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
The ideal candidate would possess:
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.
Experience with QX ONE, QX 200 and QuantStudio 7 instrumentation preferred.
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.
Qualifications
Bachelor’s degree in Biology, Chemistry, or a related scientific discipline required.
Master’s degree preferred.
4+ years of relevant industry experience; additional experience in analytical development or GMP assay validation strongly preferred.
Experience supporting late-stage development or regulated laboratory environments is preferred.
Must have authorization to work in the United States without current or future sponsorship requirements
Candidates located within a commutable distance to Berkeley, CA are highly encouraged to apply
Employment type
Full-time
Work arrangement
No
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