Quality Director/qualified Person – On Site

Ferring Pharmaceuticals

UK
**
Quality assurance and quality control
Uk/eu gmp compliance
Mhra-licensed pharmaceutical manufacturing site
** Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for their UK site, responsible for ensuring compliance with UK/EU GMP regulations and leading the Quality Assurance and Quality Control functions. The ideal candidate will have extensive pharmaceutical quality experience, a strong background in regulatory compliance, and a commitment to patient safety. **

Job Summary

  • The Quality Director is responsible for ensuring excellence in Quality, Compliance and GMP at our MHRA-licensed pharmaceutical manufacturing site, ensuring full compliance with UK/ EU GMP requirements.
  • Your day at Ferring includes ensuring compliance with UK/EU GMP regulations, providing leadership of the site Quality function (QA, QC, QMS), and performing QP batch certification and release activities.
  • Ferring is committed to building and maintaining an inclusive and diverse workplace with equal opportunities and mutual respect for all employees.

Matching Summary

Match Score: 75

** Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for their UK site, responsible for ensuring compliance with UK/EU GMP regulations and leading the Quality Assurance and Quality Control functions. The ideal candidate will have extensive pharmaceutical quality experience, a strong background in regulatory compliance, and a commitment to patient safety. **

Skills & Requirements

Must-have

  • Quality Assurance and Quality Control
  • UK/EU GMP compliance
  • MHRA-licensed pharmaceutical manufacturing site
  • Quality Management System
  • data integrity systems
  • regulatory inspections

Nice-to-have

  • entrepreneurial and innovative culture
  • speaking up is valued
  • growth and development are constant
  • cross-functional quality leadership
  • shop-floor presence

Key Requirements

  • Degree in Pharmacy, Chemistry, Microbiology, Life Sciences
  • Extensive experience in pharmaceutical quality
  • Proven expertise in batch certification
  • Fully Qualified Person (QP) under UK legislation
  • experience managing MHRA inspections

Work Rights

Not specified

Tailored Resume

Cover Letter