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
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Qa Associate in Stirling employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
