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QA Manager, IMP GMP | Lead Clinical QA & Compliance

SRG

Manchester

On-site

GBP 80,000 - 100,000

Full time

13 days ago

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Job summary

A leading CDMO in the pharmaceutical sector is seeking a Quality Assurance Manager to join their team in Manchester. This role involves ensuring compliance with UK/EU GMP standards, leading the QA team at an IMP manufacturing site, and maintaining QA systems. The ideal candidate will have over 5 years of experience in Quality Assurance within a pharma environment, provide quality oversight for product certification, and manage supplier performance. This position offers a unique opportunity for professional growth in a fast-paced environment.

Qualifications

  • Minimum of 5 years of recent experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably with IMPs.
  • Proven leadership and management experience.
  • Experience working with analytical laboratories and/or GMP production areas.

Responsibilities

  • Ensure compliance with UK/EU GMP Regulatory Standards and procedures.
  • Lead the Quality Assurance Team at an IMP manufacturing site.
  • Maintain QA systems and processes.
  • Manage documents through their lifecycle for compliance.
  • Review batch documentation and provide quality oversight for IMP certification.
  • Investigate deviations and provide support on CAPA plans.
  • Manage supplier approval and performance.
  • Conduct internal audits and implement compliance improvements.
  • Support client projects as a QA representative.
  • Provide quality training sessions.
  • Assist with regulatory inspections.

Skills

Quality Assurance leadership
GMP Compliance
Team management
Regulatory inspections

Education

Degree in a relevant scientific discipline
Job description
A leading CDMO in the pharmaceutical sector is seeking a Quality Assurance Manager to join their team in Manchester. This role involves ensuring compliance with UK/EU GMP standards, leading the QA team at an IMP manufacturing site, and maintaining QA systems. The ideal candidate will have over 5 years of experience in Quality Assurance within a pharma environment, provide quality oversight for product certification, and manage supplier performance. This position offers a unique opportunity for professional growth in a fast-paced environment.
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