Associate Director, Quality Control Compliance
Employment type
Full-time
Work setting
On-site
Location
Pennington, NJ
Schedule
Day shift
Posted
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Job overview
The Associate Director, Quality Control Compliance is an onsite role based in Pennington, NJ, at BeOne Medicines. Compensation is not specified in the posting. This role leads and manages all activities related to QC lab compliance to ensure adherence to GMP guidelines. The Associate Director will develop compliance protocols, lead investigations, and mentor staff to foster a culture of quality and continuous improvement.
What you'll do
- Develop and implement QC compliance programs
- lead laboratory investigations for OOS/OOT results
- oversee technical writing of SOPs and CAPA records
- participate in GMP audits
- mentor QC compliance staff
- collaborate with QA and Regulatory Affairs.
What we're looking for
- Skills & competencies
- full-timeday shiftpennington njbeone medicinesquality controlcompliancegmpbiotechleadershiponsiteno weekendsno on-call
- Work arrangement
- Weekend coverage required
Benefits & perks
- Not specified.
Why this role
Requires 8+ years of experience in FDA-regulated biotech/pharma and 5+ years of managerial experience.
About the employer
BeOne Medicines is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.
Additional details
- Industry sector
- 32
- Industry
- Pharmaceutical Preparation Manufacturing
- Occupation code
- 11-9199.02
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Listing ID: 49b74727-c18b-4134-b6fc-6a5a05c41990