Manager Quality Control Analytical (Sunday-Wednesday)
$112,605–$168,907 year
On-site · Rockville, Maryland, United States
Job Summary
Manager, QC Analytical leads a cGMP QC laboratory for cell therapy lot release and stability testing, overseeing sample intake, testing flow, data review, and documentation while ensuring readiness for audits and inspections. Responsibilities include managing a QC team, performing and supervising assays (flow cytometry, ELISA, PCR, cell-based assays, viability), maintaining compliant records and SOPs, training junior analysts, coordinating schedules, and driving continuous improvement (LEAN/5S) to achieve right-first-time results. The role requires strong cross-functional collaboration with Manufacturing, QA, MSAT/AD, and Supply Chain, and on-site work in the lab. Annual base pay ranges from $112,604.80 to $168,907.20, with eligibility for incentives and benefits.
Required Qualifications
- Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, or related discipline
- 5+ years' experience in pharmaceutical/biotech QC
- hands-on experience with QC instruments and lab operations in a cGMP setting
- experience coordinating lab operations, data integrity controls, and cross-functional communication
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