At a Glance
- Tasks: Review quality documentation and ensure compliance in a dynamic life science environment.
- Company: Join a growing leader in the life sciences sector with a commitment to excellence.
- Benefits: Gain valuable experience, competitive salary, and opportunities for career growth.
- Other info: Collaborative team environment with a focus on continuous improvement.
- Why this job: Kickstart your career in Quality Assurance and make a real impact on product quality.
- Qualifications: HNC/HND minimum; graduates with relevant skills are encouraged to apply.
The predicted salary is between 25650 - 31350 £ per year.
Reference: BBBH185874_1786370109QA 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 skills Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
QA Document Administrator in Stirling employer: SRG Talent
As a leading pharmaceutical development and manufacturing organisation based in central Scotland, we pride ourselves on fostering a collaborative work culture that prioritises compliance and quality. Our employees benefit from an excellent package that includes enhanced pension, healthcare, and flexible working hours, alongside ample opportunities for professional development and growth within the industry. Join us to be part of a team that values your contributions and supports your career aspirations in a meaningful way.
