Director, Quality Control

ferring.cl

Parsippany, New Jersey, United States
Base: $158,136 to $194,472; bonus: annual incentiv...
Not specified
15+ years pharmaceutical qc operations experience
Small molecule experience required
Gmp compliance and regulatory inspection management
Ferring Pharmaceuticals is seeking a Director of Quality Control in Parsippany, New Jersey, who will lead and oversee the Quality Control function, ensuring compliance with regulatory standards and managing quality systems. The ideal candidate should have extensive experience in pharmaceutical QC operations, particularly with small molecules and biologics, and demonstrate strong leadership skills

Job Summary

  • The Director will provide strategic direction for the Quality Control department to achieve corporate objectives while leading high-performing teams in a 'people first' culture.
  • Key responsibilities include overseeing manufacturing unit operations, managing third-party lab compliance, and ensuring adherence to GxP standards across commercial and development portfolios.
  • Ferring offers competitive compensation ranging from $158,136 to $194,472 base salary, along with comprehensive healthcare, 401k matching, and paid parental leave.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Director of Quality Control in Parsippany, New Jersey, who will lead and oversee the Quality Control function, ensuring compliance with regulatory standards and managing quality systems. The ideal candidate should have extensive experience in pharmaceutical QC operations, particularly with small molecules and biologics, and demonstrate strong leadership skills.

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 compliance and regulatory inspection management
  • Vendor and CMO oversight capabilities
  • Analytical and microbiological method validation

Nice-to-have

  • Biologics experience highly preferred
  • Strong coaching and mentoring skills
  • Risk-based quality system knowledge
  • Experience with Trackwise and Empower software

Key Requirements

  • Bachelor's degree plus 15+ years experience or equivalent advanced degree
  • Proven success managing FDA and global regulatory inspections
  • Small molecule experience is mandatory
  • Proficiency in MS Office, Trackwise, Oracle, Empower, and LIMS

Work Rights

Not specified

Tailored Resume

Cover Letter