Pegasus Labs

Quality Assurance Compliance Supervisor


PayCompetitive
LocationPensacola/Florida
Employment typeOther

This job is now closed

  • Job Description

      Req#: 81952

      Job Details

      Job Location: Pegasus - Pensacola, FL
      Salary Range: Undisclosed

      Pegasus Laboratories, Inc.

      Pegasus Laboratories, Inc. is a full-service Contract Development and Manufacturing Organization, or CDMO, with a very special purpose: improving the lives of animals. Through our leading veterinary brand, PRN Pharmacal, we create trusted veterinary products that promote animal wellness, including behavior modification, urinary incontinence, and seizure management. Our team of professionals, including manufacturing, quality assurance, business development, scientists and chemists, regulatory experts, and veterinarians, offers the complete package, from idea through development and regulatory approval, to production and marketing.

      Pegasus Labs, part of the PBI-Gordon Companies, Inc., is 100% employee-owned with more than 500 employee-owners, working together in pursuit of mutual success. We are growing – come join us!

      The QA Compliance Supervisor is to oversee and coordinate affairs related to QA compliance with all FDA cGMP, and other relevant regulations, and company SOPs, and to support the cGMP compliance of products.

      • Direct Supervision of QA Compliance Specialists and Doc Control Specialists
      • Final review and release of Finished Product batches
      • Review and approve returned product inspection forms and reserve sample inspection log
      • Review, revise, author SOPs and other critical documentation
      • Review and assess change controls
      • Manage the investigation process (LIs, SIRs, CAPAs, SCARs) and customer complaint process
      • Participate in internal and external audits
      • Track and report monthly metrics to Quality management
      • Generate and maintain compliance statements for materials and components

      Qualifications


      • Education: BS in a science-related field from an accredited school
      • Experience: 5 years of experience in Quality Assurance or Quality Control in a GMP regulated environment.
      • Specialized knowledge in pharmaceutical industry, cGMP environment, and FDA regulations
      • Preferred experience with electronic document management system
  • About the company

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