Quality Control Associate

Key Responsibilities: Perform in process and lot-release QC testing and characterization of stem cell derived products using validated methods. Maintain and culture stem cells utilizing aseptic techniques, including cell used as assay controls and reference material. Conduct and analyze assays including Flow Cytometry, qPCR, ELISA, Immunocytochemistry (ICC)Analyze and report results (Flow Jo, Graph Pad Prism, ImageJ) and compile data for review and Certificate of Analysis preparation. Execute sample preparation, testing, data analysis, and documentation activities. Draft and revise SOPs, test methods, and forms for the methods you run, for review and approval by others. Ensure compliance with QA/QC requirements and company procedures. Investigate deviations, document non-conformances, and support corrective and preventive actions (CAPA).Maintain logs for deviations, CAPAs, and change controls, and report open items and aging to the Director of Manufacturing and Quality. Help prepare records and evidence for internal audits. Keep QC equipment in service: routine maintenance, calibration and service scheduling, and equipment records. Manage QC reagent and consumable inventory, including lot tracking, expiry, and reorder triggers. Participate in method optimization, troubleshooting, and continuous improvement initiatives, including recurring assay problems and suggest practical fixes to existing methods Collaborate with cross-functional teams to support product development and release testing activities. Maintain accurate, timely, and compliant laboratory documentation.

Required: Master’s degree in biology, Cell Biology, Biotechnology, Molecular Biology, Biochemistry, or a related scientific field. Minimum 3 years of laboratory experience in an industry and/or research setting. At least 1 year of that experience in industry, ideally running routine testing in a QC, CRO, or other regulated or quality-managed lab. Hands-on experience with iPSC, Stem cell culture, Flow cytometry, qPCR, ELISA, Immunocytochemistry (ICC), Aseptic techniques Experience writing and revising SOPs and technical documents. Working knowledge of Good Documentation Practices and data integrity expectations. Track record of executing written procedures precisely and repeatedly, with low error rates. Strong organizational, analytical, and problem-solving skills. Excellent verbal and written communication skills.

Preferred: Exposure to document control, change control, deviations, or CAPA within a quality system (ISO 9001, GMP, or GLP).Experience with a quality management system. Experienced working in a fast-paced work environment.