Pharma QA Placement: Compliance & Documentation

Almac Group; Craigavon; On-site; GBP 18,000 - 24,000; Full time

Job summary

Almac Group is seeking a detail-focused student to join the Quality team at the Craigavon headquarters. You will support QA projects, coordinate activities, and assist with quality documentation across the drug development lifecycle.

The placement will provide exposure to GMP, quality systems, product compliance, and cross-functional collaboration. Hours are 37.5 per week for a 12-month period from July 2027 to July 2028.

Qualifications

• Five GCSEs, or equivalent, at Grade C or above, including English Language and Mathematics.
• Currently studying a science or technical degree, with successful completion of two years.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office applications, including Excel, Word, Project, Outlook and PowerPoint.
• High attention to detail, strong planning skills and the ability to process and analyse technical information.

Responsibilities

• Support Good Manufacturing Practice compliance and the quality of manufactured and released pharmaceutical products.
• Provide quality assurance support to operational teams working on new and existing products and projects.
• Help review quality records including deviations, corrective and preventative actions, change controls, complaints and out-of-specification reports.
• Review production, laboratory, validation and stability information for accuracy and completeness.
• Assist with Good Manufacturing Practice documentation, internal audits, technical agreements, compliance metrics and efficiency projects.

Skills

Quality Assurance

Documentation Review

GMP

Education

GCSEs and Year 2 Science/Technical degree

Job description

Almac Group is seeking a detail-focused student to join the Quality team at the Craigavon headquarters. You will support QA projects, coordinate activities, and assist with quality documentation across the drug development lifecycle.

The placement will provide exposure to GMP, quality systems, product compliance, and cross-functional collaboration. Hours are 37.5 per week for a 12-month period from July 2027 to July 2028.