GMP Quality Compliance Auditor (Pharma)

Almac Group; Craigavon; On-site; GBP 42,000 - 64,000; Full time

Job summary

Almac Group is seeking a Quality Compliance Auditor to support GMP compliance for Drug Substance and Drug Product manufacturing for the UK and Ireland. The role reports to the Clinical Services unit and is based in Craigavon with office-based duties.

You will collaborate with Qualified Persons, ensure timely regulatory submissions, and uphold high quality standards in a fast-paced, regulated environment. After initial six months in-office, hybrid working may be considered under applicable terms.

Qualifications

• Must have a Bachelor's degree in biology, pharmacy, chemistry or related subject.
• Relevant experience in a pharmaceutical manufacturing, laboratory or GMP environment.
• Eligible to work in the UK without restrictions or hold a valid work permit for full-time employment in the UK.

Responsibilities

• Support Almac Clinical Services' Qualified Persons in the UK and Ireland to ensure GMP compliance across Drug Substance and Drug Product manufacture.
• Work to internal timelines and regulatory expectations to maintain high quality standards.
• Contribute to delivering vital medicines to patients by upholding quality and compliance.

Skills

Organisational skills

Problem-solving abilities

Effective communication

Attention to detail

Relationship building

Education

Bachelor's degree in biology/pharmacy/chemistry

Job description

Almac Group is seeking a Quality Compliance Auditor to support GMP compliance for Drug Substance and Drug Product manufacturing for the UK and Ireland. The role reports to the Clinical Services unit and is based in Craigavon with office-based duties.

You will collaborate with Qualified Persons, ensure timely regulatory submissions, and uphold high quality standards in a fast-paced, regulated environment. After initial six months in-office, hybrid working may be considered under applicable terms.