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Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Manager, Production Compliance

Validation, Compliance & Quality SystemsPosted on Nov 10
Full-timeParsippany-Troy Hills, NJ, USA

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Engineering, or a related field is required.
  • At least 7 years of experience in GMP manufacturing or quality assurance, including at least 3 years in a compliance or investigations role, is required.
  • At least 2 years of people-management or team-leadership experience is required.
  • Strong knowledge of FDA regulations, current Good Manufacturing Practice (cGMP), and quality systems is required.
  • Problem-solving, root-cause-analysis, and corrective and preventive action (CAPA) design skills are required.
  • Excellent written and verbal communication skills are required.
  • The ability to manage multiple priorities in a fast-paced manufacturing environment is required.
  • The employee must be able to stand, walk, and sit for extended periods, including during floor investigations, line walkthroughs, and audits.
  • The employee must be able to bend, stoop, reach, and climb stairs, platforms, or ladders to observe equipment and processes.
  • The employee must occasionally lift and carry up to 25 pounds, such as batch records, samples, or small equipment.
  • The employee must qualify for and wear full cleanroom gowning, follow cleanroom hygiene rules, complete gowning qualification, and participate in ongoing aseptic behavior training.
  • The employee must wear required personal protective equipment, including safety glasses, hearing protection, and safety shoes, and work around cleaning and sanitizing agents and moving equipment while following site safety procedures.
  • The employee must be able to use a computer, keyboard, and phone for extended periods.
  • The employee must be able to work extended hours, off-shift, or weekends occasionally to support investigations, audits, or production events.

Responsibilities

  • Lead, manage, and develop a team of Compliance Specialists responsible for deviations, non-conformances, and manufacturing incidents.
  • Ensure investigations are completed in a timely manner with appropriate documentation, root-cause analysis, and regulatory compliance.
  • Serve as the subject-matter expert for investigations.
  • Drive consistent use of root-cause-analysis tools, such as 5 Whys, Fishbone, and Fault Tree.
  • Oversee implementation of production corrective and preventive actions, including performing effectiveness checks and follow-up activities.
  • Provide regular reporting on deviation trends and metrics to site leadership.
  • Identify systemic issues and collaborate with site functions to prevent recurrence.
  • Serve as lead liaison with quality assurance, quality control, Operations, Engineering, and Supply Chain during investigations.
  • Support regulatory inspections and internal audits by providing investigation records and justifications.
  • Represent the site’s investigation programs, if applicable.

Desired Qualifications

  • An advanced degree is preferred.
  • Experience with TrackWise or a similar electronic quality system is preferred.

About the Company

Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Ferring Pharmaceuticals develops medicines that use the body's own peptide hormones, focusing on specialties such as reproductive health, gastroenterology, and urology. Its products range from hormone-based therapies to newer gene-based treatments, such as Adstiladrin for bladder cancer. The company achieves its solutions through research-driven development and manufacturing, including synthetic production of peptide hormones (historically oxytocin and vasopressin) and ongoing expansion of production and clinical programs. Ferring differentiates itself by remaining privately held to pursue a long-term research vision, growing through organic expansion and strategic acquisitions while maintaining a global footprint (over 100 countries, 7,000+ employees). Its goal is to advance therapies that leverage the body's biology to treat diseases more effectively, supported by a sustained investment in R&D and manufacturing, with a future focus on bioengineered and gene-based approaches.

Company size
5,001-10,000
Company stage
Debt Financing
Total funding
$302.5M
Headquarters
Saint-Prex, Switzerland
Founded
1950

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