Director, Quality Control

ferring.fr

Parsippany, United States
Base: $158,136 to $194,472; bonus/equity: competit...
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Strategic leadership of quality control
Oversight of analytical and microbiology
Vendor oversight and data review
** Ferring is seeking a Director of Quality Control in Parsippany, New Jersey, responsible for leading the Quality Control function, ensuring compliance, and overseeing analytical and microbiological testing. The ideal candidate should have extensive experience in pharmaceutical quality control, particularly with small molecules and biologics. **

Job Summary

  • As Director, Quality Control, you will be responsible for 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.
  • Key responsibilities include vendor oversight, data review, external audits, and management of GMP-related exceptions (e.g., deviations, CAPAs, OOS/OOT, change controls).
  • Ferring offers competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities.

Matching Summary

Match Score: 75

** Ferring is seeking a Director of Quality Control in Parsippany, New Jersey, responsible for leading the Quality Control function, ensuring compliance, and overseeing analytical and microbiological testing. The ideal candidate should have extensive experience in pharmaceutical quality control, particularly with small molecules and biologics. **

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

  • strategic leadership of Quality Control
  • oversight of Analytical and Microbiology
  • vendor oversight and data review
  • GMP-related exceptions management
  • method transfers and validation oversight
  • cGMP documentation approval

Nice-to-have

  • entrepreneurial spirit and long-term perspective
  • people first philosophy
  • science and research commitment
  • innovative company recognition

Key Requirements

  • 15+ years of experience in pharmaceutical QC operations
  • Bachelor's degree in a scientific discipline
  • Small molecule experience required
  • Proven success managing regulatory inspections
  • Proficient in MS Office, Trackwise, Oracle, Empower, and LIMS

Work Rights

Not specified

Tailored Resume

Cover Letter