Director, Quality Control

FERRING PHARMACEUTICALS AS

Parsippany, New Jersey, United States
Base: $158,136 to $194,472; bonus: annual incentiv...
15+ years pharmaceutical qc operations experience
Small molecule experience required
Gmp testing oversight at cmos
The Director will provide strategic direction for the Quality Control department to achieve corporate objectives while leading a high-performing team in analytical and microbiological testing

Job Summary

  • The Director will provide strategic direction for the Quality Control department to achieve corporate objectives while leading a high-performing team in analytical and microbiological testing.
  • This role requires deep expertise in managing GMP-related exceptions, overseeing third-party labs, and ensuring compliance with FDA and global regulatory standards across development and commercial portfolios.
  • Ferring offers a competitive base salary ranging from $158,136 to $194,472, along with comprehensive benefits including healthcare, 401k matching, and paid parental leave.

Matching Summary

The Director will provide strategic direction for the Quality Control department to achieve corporate objectives while leading a high-performing team in analytical and microbiological testing.

Salary

Base: $158,136 to $194,472; Bonus: Annual incentive compensation based on performance; Benefits: Comprehensive healthcare, 401k match, paid parental leave, 15 holidays

Skills & Requirements

Must-have

  • 15+ years pharmaceutical QC operations experience
  • Small molecule experience required
  • GMP testing oversight at CMOs
  • FDA and global regulatory inspection management
  • Vendor audit and third-party lab oversight

Nice-to-have

  • Biologics experience highly preferred
  • Risk-based quality systems knowledge
  • Strong coaching and mentoring skills
  • Experience with Trackwise, Oracle, Empower
  • Cross-functional collaboration capabilities

Key Requirements

  • Bachelor's degree in scientific discipline with 15+ years experience
  • Master's degree with 12+ years or PhD with 10+ years acceptable
  • Small molecule experience is mandatory
  • Proven success managing FDA and global regulatory inspections

Work Rights

Not specified

Tailored Resume

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