CK Group are recruiting for a Quality Assurance Specialist to join a leading global diagnostics company based in Southampton on a permanent basis.
The Company:
Our client are experts in the development, manufacture, and distribution of high-quality molecular diagnostic products. They have customers in many different industries including academia, research, diagnostics, food industry and the veterinary industry selling to over 100 countries worldwide.
Location:
This is an onsite role based in Southampton.
Main duties and responsibilities will include to be:
- Responsible for document management system(s)
- Assure ongoing compliance with quality and industry regulatory requirements including ISO 9001.
- Assist the business to support the Quality management system in place.
- Identify training needs and organise training interventions to meet quality standards.
- Ensure the timely release of compliant, safe, functioning products through collaboration with all departments.
- Document internal audits and other Quality Assurance activities
- Provide guidance to achieve timely release of compliant products, leading to increased customer satisfaction and safety.
- Investigate non-conformance issues and identify root cause and implementation of corrective and preventive actions.
- Perform internal audits and supplier audits as required.
- Support on-site audits conducted by external providers.
Your Background:
- Prior experience in a Quality Assurance role working to ISO 9001 standards.
- Experience of documentation control, batch release, Out of Specification (OOS), Change Control, Non-Conformances, Root cause analysis and CAPA.
- Knowledge of Good Documentation and Manufacturing Practice is also desired.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56629 in all correspondence.