About this role
Join a Growing Life Science Leader!
About the Opportunity
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
- HNC/HND minimum; degree preferred
- 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
Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.