CK Group are recruiting for a QA Document Controller to join a product development company in the life science industry at their site based in Stokesley on a permanent basis.
Our client is part of a biotechnology group, focused on the design, manufacture, validation and supply of real-time PCR kits and reagents.
As a QA Document Controller, you will be responsible for the maintenance of quality system documentation. This will include handling and storage of quality documentation, ensuring seamless document access across departments.
Your main duties will be:
- Filing and archiving relevant quality documentation, both hard copy and electronic documents
- Reporting errors or developments regarding document storage
- Ensuring the secure destruction and disposal of sensitive documents
- Participation in QA activities and team meetings
-Previous experience of controlling QMS documentation.
-Experience of working to GMP standards
Entitlement to work in the UK is essential. Please quote reference 50856.
You must be eligible to work in the UK. Learn more
- Agency: CK Group
- Contact: Phoebe Walker
- Phone: 01246 457700
- Reference: 50856
Website: CK Group
- Posted: 11th June 2021
- Expires: 9th July 2021