Quality Director/qualified Person – On Site

Ferring B.V

East Kilbride, United Kingdom
Uk/eu gmp compliance
Quality management system oversight
Batch certification and release
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

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.
  • Creating and delivering life-changing products means getting it right first time is a shared responsibility, so our global manufacturing teams work closely together to ensure quality, accuracy and safety at all times.
  • Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role.

Matching 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.

Skills & Requirements

Must-have

  • UK/EU GMP compliance
  • Quality Management System oversight
  • Batch certification and release
  • MHRA inspection management
  • Data integrity systems management
  • Cross-functional quality leadership

Nice-to-have

  • Strong stakeholder engagement
  • Continuous improvement initiatives
  • Commitment to patient safety
  • Operational visibility on shop floor
  • Support regulatory submissions

Key Requirements

  • Degree in Pharmacy, Chemistry, Microbiology, Life Sciences or related
  • Extensive pharmaceutical quality GMP manufacturing experience
  • Fully Qualified Person (QP) under UK legislation
  • Proven experience managing MHRA inspections
  • Strong knowledge of EU/UK GMP, ICH guidelines, MHRA expectations
  • Experience with oral solid dosage pharmaceutical products

Work Rights

Not specified

Tailored Resume

Cover Letter