About the role
Job Summary
The Quality Control Associate performs cGMP release and in-process testing for cell therapy products, ensuring compliance with cGMP regulations, SOPs, and quality standards.
Key Responsibilities
- Perform cGMP release testing using cell counting, flow cytometry, ELISA, cell-based cytotoxicity assays, and digital PCR (dPCR).
- Document and review analytical results in compliance with cGMP requirements.
- Maintain laboratory equipment and support routine QC operations.
- Ensure adherence to SOPs, data integrity, and quality standards.
Qualifications
- Bachelor's degree in Biology or a related Life Sciences field with 1–2 years of relevant cGMP laboratory experience, or
- Associate's degree in Biology or a related field with 2–3 years of relevant cGMP laboratory experience.
- Hands-on experience with cell-based analytical techniques and cGMP laboratory practices preferred.
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