QA Document Reviewer

SRG; Stirling; On-site; GBP 26,000 - 38,000; Full time

Job summary

SRG is expanding its QA team and is seeking a QA Document Reviewer to support the Quality Assurance function. You will review quality and batch documentation in a regulated GMP environment, ensuring accuracy and control across the business.

This role is suitable for motivated science graduates looking to start a career in QA, with opportunities to learn GMP systems, maintain documentation trackers, and contribute to continuous QA improvement under the QA Manager.

Qualifications

• Experience reviewing quality or batch documentation in a regulated GMP environment preferred, graduates with demonstrable skills also considered.
• Strong written and verbal communication skills at all levels.
• Knowledge of Quality Systems is desirable.

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.

Skills

Attention to detail

Document review

GMP awareness

Communication skills

Organisational skills

Analytical thinking

Data entry

Tools

Microsoft Office

Job description

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

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

This role is also suitable for driven science graduates looking to start their career in QA.

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 graduates with demonstrable skills
• 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