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.
• Collaborate 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 cell biology analytical methods, including cell count and viability, high-resolution imaging, live-cell imaging, and cell-based potency assays.
• Experience with fluorescence microscopy, Incucyte, and Cytation instrumentation preferred.
• Experience with HPLC is a plus.
• 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 Cell Biology, 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
Mon-Friday 1st Shift, No weekend or holiday work
What we offer:
• Comprehensive medical coverage, with dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid holidays and vacation
• Comp Range: $60,000-80,000
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.
#LI-EB1
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.