Details:
- Job Type: Permanent
- Job Status: Full-Time
- Location: Stirling
- Date: 2 days ago
Description:
QA Document Reviewer
Join a Growing Life Science Leader!
About the Opportunity
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'll 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
HNC/HND minimum; degree preferred
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 skillsGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy