Quality Director/qualified Person – On Site

FERRING PHARMACEUTICALS AS

East Kilbride, United Kingdom
Onsite
Uk/eu gmp compliance
Batch certification and release
Quality management system leadership
Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for its East Kilbride site, responsible for ensuring compliance with UK and EU GMP regulations. The role involves leadership in Quality Assurance and Quality Control while maintaining a culture of empowerment and collaboration

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

Match Score: 85

Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for its East Kilbride site, responsible for ensuring compliance with UK and EU GMP regulations. The role involves leadership in Quality Assurance and Quality Control while maintaining a culture of empowerment and collaboration.

Skills & Requirements

Must-have

  • UK/EU GMP compliance
  • batch certification and release
  • Quality Management System leadership
  • MHRA inspection management
  • pharmaceutical manufacturing environment
  • data integrity systems management
  • cross-functional quality leadership

Nice-to-have

  • continuous improvement initiatives
  • stakeholder engagement and communication
  • risk-based quality decision making
  • commitment to patient safety
  • inclusive and diverse workplace culture

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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