Quality Director/qualified Person – On Site

Ferring Pharmaceuticals

United Kingdom
Onsite
Uk/eu gmp compliance
Quality assurance and quality control
Mhra inspections
Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for their UK site, focusing on ensuring compliance with UK/EU GMP requirements in pharmaceutical manufacturing. The role requires significant experience in quality assurance and regulatory compliance, along with strong leadership and stakeholder engagement skills

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.
  • The role holds strategic and operational accountability for Quality Assurance and Quality Control.
  • Ferring Pharmaceuticals is committed to building families and living better lives through scientific advances and a culture of empowerment and continuous development.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Quality Director/Qualified Person for their UK site, focusing on ensuring compliance with UK/EU GMP requirements in pharmaceutical manufacturing. The role requires significant experience in quality assurance and regulatory compliance, along with strong leadership and stakeholder engagement skills.

Skills & Requirements

Must-have

  • UK/EU GMP compliance
  • Quality Assurance and Quality Control
  • MHRA inspections
  • Quality Management System
  • data integrity systems
  • patient safety and product quality

Nice-to-have

  • entrepreneurial and innovative
  • speaking up is valued
  • growth and development are constant
  • shop-floor presence
  • continuous improvement initiatives

Key Requirements

  • Degree in Pharmacy, Chemistry, Microbiology, Life Sciences, or related discipline
  • Extensive experience in pharmaceutical quality within a GMP manufacturing environment
  • Proven expertise in batch certification and regulatory compliance
  • Strong knowledge of EU/UK GMP, ICH guidelines, MHRA expectations
  • Fully Qualified Person (QP) under UK legislation
  • Proven experience managing MHRA inspections

Work Rights

Not specified

Tailored Resume

Cover Letter