Associate Director, QA & GMP Compliance (Biologics)

Confidential; Cranbury Township (NJ); On-site; USD 100,000 - 180,000; Full time

Job summary

A leading global biologics technology platform is seeking an Associate Director for Quality Assurance in Cranbury, NJ. This role focuses on establishing and improving Quality Management Systems supporting GMP clinical manufacturing. Successful candidates will have extensive experience in the pharmaceutical industry, strong problem-solving skills, and the ability to lead quality initiatives. The position offers a competitive salary range of $100,000 to $180,000 annually.

Qualifications

• Minimum 14 years of experience in pharmaceutical/biotechnology industry.
• In-depth knowledge of cGMP and guidelines.
• Hands-on experience with pharmaceutical system validation.
• Experience with Quality Management Computer Systems.

Responsibilities

• Establish and continuously improve Quality Management Systems.
• Review clinical batch records and associated deviations.
• Lead the implementation of key performance indicators for QMS.
• Manage internal audit programs and process improvements.
• Recruit, train, and manage staff.

Skills

Critical thinking

Problem-solving

Technical writing

Communication

Team collaboration

Adaptability

Tools

Master Control

SAP

Job description

A leading global biologics technology platform is seeking an Associate Director for Quality Assurance in Cranbury, NJ. This role focuses on establishing and improving Quality Management Systems supporting GMP clinical manufacturing. Successful candidates will have extensive experience in the pharmaceutical industry, strong problem-solving skills, and the ability to lead quality initiatives. The position offers a competitive salary range of $100,000 to $180,000 annually.