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 skills

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.