Sr Manager GMP Quality

Primary Responsibilities

• Contribute to day-to-day GMP Quality operations, including batch record review and release, deviation management, change control, product complaints, and other quality processes.

Skills & Requirements

• Hands-on experience in GMP Quality Operations, with a strong background in batch disposition and QMS processes.
• Proficiency in managing deviations, change control, CAPAs, and product complaints.
• Experience with small-molecule drug substances and oral solid dosage forms (e.g., capsules, tablets) is strongly preferred.
• Ability to work independently and provide proactive Quality support in a fast-paced environment.
• Familiarity with Veeva Docs/QMS systems is a plus.