Director, Quality Control

Ferring B.V

Parsippany, United States
Base: $158,136 to $194,472; bonus/equity: competit...
On-site
Quality control (analytical and microbiology)
Method transfers, validations, and data oversight
Vendor oversight and external audits
Ferring B.V. is seeking a Director of Quality Control in Parsippany, New Jersey, to lead the Quality Control function, focusing on analytical and microbiology testing. The ideal candidate will have extensive experience in pharmaceutical QC operations and a strong background in regulatory compliance

Job Summary

  • Provide strategic leadership and oversight of the Quality Control (Analytical and Microbiology) function, including testing at contract labs for drug substance, drug product, and stability programs.
  • Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC Regulatory Affairs to manage method transfers, validations, and data oversight aligned with development and production timelines.
  • At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

Matching Summary

Match Score: 85

Ferring B.V. is seeking a Director of Quality Control in Parsippany, New Jersey, to lead the Quality Control function, focusing on analytical and microbiology testing. The ideal candidate will have extensive experience in pharmaceutical QC operations and a strong background in regulatory compliance.

Salary

Base: $158,136 to $194,472; Bonus/Equity: Competitive annual incentive compensation targets in the form of an annual bonus; Benefits: Comprehensive healthcare, 401k plan and company match, disability coverage, life insurance, wellness benefits, tuition reimbursement, sick time, vacation time, 15 paid holidays, paid parental leave

Skills & Requirements

Must-have

  • Quality Control (Analytical and Microbiology)
  • method transfers, validations, and data oversight
  • vendor oversight and external audits
  • GMP-related exceptions management
  • specification setting and trending
  • cGMP documentation approval

Nice-to-have

  • life-changing therapies
  • entrepreneurial spirit
  • people first philosophy
  • science and research commitment

Key Requirements

  • Bachelor's degree in scientific discipline with 15+ years of experience
  • Master's degree with 12+ years of experience
  • PhD with 10+ years of experience
  • Small molecule experience required
  • Biologics experience highly preferred
  • Proficient in MS Office, Trackwise, Oracle, Empower, and LIMS

Work Rights

Not specified

Tailored Resume

Cover Letter