Quality Control Lead

About the RoleThe candidate will support technical documentation required for BLA submission, and ensure the QC organization is inspection ready. This position will also coordinate QC schedules, resource allocation, and testing timelines critical for successful BLA submission. ResponsibilitiesSupport preparation and review of technical reports and QC documentation required for the BLA, ensuring timely completion and regulatory accuracy. Create, maintain, and monitor QC testing trackers, documenting tests, timelines, assigned analysts, sample workflows, and status updates. Facilitate and maintain a resource loading tracker, aligning personnel capacity with sample testing volume to ensure on-time data generation for the BLA. Escalate resource gaps, workflow delays, or testing challenges that could impact critical milestones. Support method transfer and method validation troubleshooting to ensure analytical readiness for BLA submission. Lead the establishment and maintenance of a stability program, ensuring data availability for regulatory filing. Participate in internal and external GMP audits, ensuring QC operations meet all regulatory expectations. Required QualificationsBachelors degree in Chemistry, Biochemistry, Biotechnology, Biology, required 5+ years of experience in an FDA-regulated pharmaceutical with demonstrated experience supporting major regulatory submissions (e.g., BLA, NDA, MAA). 5+ years of experience in analytical chemistry methods including HPLC, UPLC, GC, TOC, and related instrumentation. Strong working knowledge of USP/EP, cGMP, EU GMP, and analytical compliance requirements. Proven experience tracking testing deliverables, coordinating QC schedules Preferred SkillsTechnical writing expertise, including investigations, method documents, validation protocols/reports, and change control assessments. Ability to prioritize multiple deliverables and manage time effectively in a high-pressure, deadline-driven environment, especially in support of regulatory filing timelines.