QA Associate

As a Quality Assurance Associate, you ensure documentation excellence in a regulated life science environment. You will support document control, review quality and batch records, and help maintain compliant data and records. The role sits within the Quality Assurance function and partners across the business to uphold GMP/quality systems standards. You’ll contribute to continuous QA improvement and timely documentation updates. This is a hands-on role for detail-oriented professionals with a passion for regulatory quality.

• Review quality and batch documentation with accuracy and attention to detail
• Provide document control support and guidance across the business
• Maintain trackers and generate status reports to support batch compilation
• Support document archiving and ensure controlled movement of materials
• Coordinate SOP review cycles and ensure timely revisions
• Ensure documents are updated, mastered, and maintained per procedures
• Contribute to GMP compliance activities and continuous QA improvement

• HNC/HND minimum; degree preferred
• Experience in document review within a regulated GMP environment (or ISO 9001/13485 background)
• Strong written and verbal communication skills
• Knowledge of Quality Systems (desirable)
• Excellent organisational skills and ability to work independently or in a team
• Analytical problem-solving and decision-making
• Proficiency in Microsoft Office and confident data entry

• clear communication
• team collaboration
• analytical mindset
• document control
• GMP knowledge
• ISO 9001/13485 awareness