QA Documentation Specialist – GMP/ISO Records

Srg; Stirling; On-site; GBP 26,000 - 36,000; Full time

Job summary

Srg, a life sciences organisation in Stirling, UK, seeks a Quality Assurance Associate to support the QA function and ensure documentation excellence across the business.

You will review quality and batch documentation, provide document control, maintain trackers, and support archiving, while contributing to GMP/ISO compliance and QA improvements. This role suits someone with a data review background in regulated industries.

Qualifications

• Experience reviewing quality or batch documentation in GMP/regulatory environments.
• Strong written and verbal communication skills at all levels.
• Proficiency with Microsoft Office; data-entry accuracy.

Responsibilities

• Review quality and batch documentation with accuracy and attention to detail.
• Provide document control functions, support, and guidance across the business.
• Maintain trackers and generate status reports for batch compilation activities.
• Support document archiving, ensuring controlled and compliant material movement.
• Coordinate SOP reviews and ensure revisions meet timelines.
• Ensure documents are updated, mastered, and maintained per procedures.
• Contribute to GMP compliance activities and continuous QA improvement.

Skills

Attention to detail

Analytical

Organisational

Tools

Microsoft Office

Job description

Srg, a life sciences organisation in Stirling, UK, seeks a Quality Assurance Associate to support the QA function and ensure documentation excellence across the business.

You will review quality and batch documentation, provide document control, maintain trackers, and support archiving, while contributing to GMP/ISO compliance and QA improvements. This role suits someone with a data review background in regulated industries.