Pharma Quality & Compliance Officer — Hybrid

Perrigouk; Dodworth; Hybrid; GBP 42,000 - 62,000; Full time

Benefits offered by this job

Hybrid Working Approach

Competitive compensation and benefits

Job summary

Perrigo in the United Kingdom is seeking a highly motivated Quality & Compliance Officer (Pharma) to join our Quality team and support the release and distribution of pharmaceutical products in a regulated environment.

Reporting to the Quality function, you will manage batch documentation, coordinate samples, support QPs, and maintain quality records in accordance with GDP, GMP, and regulatory requirements, fostering a culture of compliance.

Qualifications

• Experience in the pharmaceutical industry is required.
• Experience in Quality Assurance, Quality Compliance, or Quality Operations.
• Experience in a regulated GMP and/or GDP environment.
• Understanding of pharmaceutical batch documentation, product release processes, and quality systems.
• Degree in a scientific discipline is advantageous; equivalent industry experience will also be considered.

Responsibilities

• Review and verify batch documentation for imported pharmaceutical products.
• Coordinate dispatch of samples to contract testing laboratories.
• Maintain quality records and documentation per regulatory requirements.
• Support Qualified Persons (QPs) to ensure batches are complete and ready for certification.
• Coordinate document control, archiving, and retention processes.
• Prepare and distribute weekly testing and batch release schedules.

Skills

Quality management

Quality & Compliance

GMP/GDP

Excel

SharePoint

SAP

Communication skills

Education

Scientific degree

Tools

SAP

Excel

Outlook

SharePoint

Job description

Perrigo in the United Kingdom is seeking a highly motivated Quality & Compliance Officer (Pharma) to join our Quality team and support the release and distribution of pharmaceutical products in a regulated environment.

Reporting to the Quality function, you will manage batch documentation, coordinate samples, support QPs, and maintain quality records in accordance with GDP, GMP, and regulatory requirements, fostering a culture of compliance.