Sr. QC Specialist - Analytical - 174633 - 175532

Responsibilities: of the QC Specialist - Analytical: • Perform QC analytical testing in a cGMP laboratory to support product release and stability testing • Execute molecular assays including PCR, qPCR, and/or ddPCR, along with other nucleic acid-based testing • Perform analytical assays such as flow cytometry, ELISA/MSD, cell viability, cell enumeration, and characterization testing • Analyze and trend laboratory data while maintaining accurate documentation in accordance with cGMP and Good Documentation Practices (GDP) • Support laboratory investigations, deviations, OOS/OOT events, and CAPA activities as needed • Author and revise SOPs, technical reports, and other controlled documentation • Operate, maintain, and troubleshoot analytical laboratory instrumentation Qualifications: of the QC Specialist - Analytical: • Bachelor's degree in Molecular Biology, Biology, Biotechnology, Biochemistry, or a related scientific discipline • 3+ years of QC analytical experience in a cGMP biotechnology, biologics, cell therapy, or pharmaceutical environment • Hands-on experience with PCR, qPCR, ddPCR, or other molecular assay platforms • Experience performing QC analytical testing for product release in a GMP laboratory • Exposure to DNA/RNA sequencing, ELISA/MSD, or flow cytometry is highly preferred • Strong understanding of cGMP regulations and Good Documentation Practices (GDP) Compensation: for the QC Specialist - Analytical: • Pay Rate: $35-40/hr. • Contract-to-Hire • Comprehensive Benefits: Medical, Dental, Vision, 401(k), Sick Leave (as required by law), and Paid Holidays Application Period: This position opens for applications on 7/21/2026 and will remain open for a minimum of 30 days from the posting date.