Qa Associate

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

Are you experienced in reviewing quality or batch documentation in a regulated environment?

This expanding life science organisation is seeking a committed Quality Assurance Associate to support their Quality Assurance function and ensure documentation excellence across the business.

This role is also suitable for people with a strong Quality or data review background in food and drink or the medical device and similarly regulated industries.

Reporting to the Quality Assurance Manager, you will play a critical role in maintaining compliant, accurate, and well controlled documents, data, and records.

Key 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 accurate status reports to support batch compilation activities
• Support document archiving, ensuring controlled and compliant material movement
• Coordinate SOP review cycles and ensure revisions meet required timelines
• Ensure all documents are updated, mastered, and maintained according to established procedures
• Contribute to GMP compliance activities and continuous QA improvement

Requirements

• Experience in document review within a regulated GMP environment is preferred but they will consider people from an ISO 9001 or ISO13485 background.
• Strong written and verbal communication skills at all levels
• Knowledge of Quality Systems (desirable)
• Excellent organisational skills, with the ability to work independently and as part of a team
• Analytical approach to problem solving and decision making
• Proficiency in Microsoft Office and confident data entry skills