Director, Quality Assurance – Batch Release & Customer Relationship

Thermo Fisher Scientific UK

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10+ years cgmp pharmaceutical experience
5+ years steriles manufacturing experience
8+ years leadership role experience
** Thermo Fisher Scientific UK is seeking a Director of Quality Assurance focused on batch release and customer relationships to ensure compliance with internal standards and regulatory requirements. The role emphasizes strategic oversight, customer advocacy, and continuous improvement in quality processes within the pharmaceutical industry. **

Job Summary

  • The Director provides strategic quality oversight for batch release and customer support to ensure full compliance with internal standards and regulatory requirements.
  • This role serves as a key quality liaison for customers, fostering strong relationships and addressing quality concerns directly.
  • The position requires developing technical and managerial staff while collaborating with operations to promote good manufacturing practices and improve quality culture.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific UK is seeking a Director of Quality Assurance focused on batch release and customer relationships to ensure compliance with internal standards and regulatory requirements. The role emphasizes strategic oversight, customer advocacy, and continuous improvement in quality processes within the pharmaceutical industry. **

Skills & Requirements

Must-have

  • 10+ years cGMP pharmaceutical experience
  • 5+ years steriles manufacturing experience
  • 8+ years leadership role experience
  • Batch record review and release expertise
  • Customer relationship management in QA
  • Regulatory inspection support capability

Nice-to-have

  • CDMO or contract manufacturing environment
  • Compliance turnaround program experience
  • Advanced change management skills
  • Matrixed organization leadership
  • Proactive risk mitigation strategy

Key Requirements

  • Bachelor's degree in Physical Sciences or Engineering
  • 10+ years cGMP experience in pharmaceutical industry
  • 5+ years steriles manufacturing experience
  • 8+ years in a leadership role
  • Experience influencing senior organizational levels

Work Rights

Not specified

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