QA Specialist — Pharma GMP & Continuous Improvement

Ipsen; Wrexham; On-site; GBP 60,000 - GBP 80,000; Full time

Job summary

A leading pharmaceutical company in Wrexham is seeking a QA professional to provide oversight in documentation and processes during facility set-up. Key responsibilities include supporting batch record reviews and leading investigations into deviations. The ideal candidate will have experience in the pharma industry, strong knowledge of GMP and regulatory requirements. Join a dynamic team committed to excellence and innovation in pharmaceutical manufacturing.

Qualifications

• Experience in a similar role in pharma or biopharma.
• Strong knowledge of GMP, validation, and regulatory requirements.
• Experience in sterile manufacturing environments and batch release is highly preferred.

Responsibilities

• Provide QA oversight for documentation and processes during facility set-up.
• Support batch record review and ensure timely, compliant batch release.
• Lead investigations into deviations, OOS, CAPAs, and change controls.
• Deliver training and guidance on GMP and quality standards.
• Represent QA in site projects and regulatory inspections.
• Drive continuous improvement and promote a proactive quality culture.

Skills

Experience in a similar role

Knowledge of GMP

Experience in sterile manufacturing

Strong knowledge of regulatory requirements

Job description

A leading pharmaceutical company in Wrexham is seeking a QA professional to provide oversight in documentation and processes during facility set-up. Key responsibilities include supporting batch record reviews and leading investigations into deviations. The ideal candidate will have experience in the pharma industry, strong knowledge of GMP and regulatory requirements. Join a dynamic team committed to excellence and innovation in pharmaceutical manufacturing.