Manager, Quality - QC Analytical

The Quality Control Manager oversees all QC laboratory operations and testing activities, supervises QC staff, and ensures compliant and efficient lab execution, maintains cGMP compliance and data integrity.

Requirements

• 8+ years of experience in analytical chemistry within Pharmaceutical QC environment.
• Minimum of 1 year of previous management experience in Pharmaceutical QC laboratory, including supervision of QC chemists.
• Leadership skills, ability to prioritize workload, mentor staff, and ensure inspection readiness and cGMP compliance.
• Experience managing and overseeing external contract testing laboratories (CROs/CMOs) is preferred.
• Understanding of analytical platforms including HPLC, FTIR, UV/Vis, and Drug Release.
• Experience overseeing analytical method validation, verification, method transfer activities, and management of cGMP stability programs.
• Working knowledge of ICH guidelines, major pharmacopoeias (USP, Ph. Eur., JP), CTD structure, and global regulatory expectations.
• Analytical skills (interpret data, summarize data, present data), written and verbal communication skills.
• Ability to work independently, within a team, personal integrity, credibility, and responsibility.
• Excellent organizational skills, ability to work on multiple projects/tasks, meets milestones and schedules.
• Bachelor’s degree in a scientific discipline is required

Benefits

• Company sponsored relocation assistance
• Generous Paid Time Off