Validation Manager

3 weeks ago

Great Yarmouth, United Kingdom CK GROUP Full time

CK Group are recruiting for a Validation Manager to join a pharmaceutical company at their site in Great Yarmouth on a permanent basis.
**The Company**:
Our client has over 55 years experience focused on researching and developing innovative dermatological treatments.
**Validation Manager Role**:

- Reviewing and approving all validation plans, protocols and reports
- Executing cleaning validation protocols at all sites
- Managing projects and existing installations for temperature mapping / monitoring across sites.
- Raising and managing change controls for assigned projects.
- Preparing, controlling, reviewing, and approving Quality documentation to align with QMS.
- Maintaining awareness of upcoming regulatory environment.
- Assisting other departments involved in validation activities including validation of equipment, processes, and the preparation of associated documentation.
- Liaising with the Computer System Validation team to ensure such aspects are covered during the execution of protocols.

**Your Background**:

- Several years relevant quality experience in a pharmaceutical GxP environment.
- Degree or equivalent in appropriate scientific discipline.
- Experience of writing protocols, reports and executing Equipment & Facilities Validations, Cleaning Validations and Process Validations..
- Understanding of GAMP requirements for computer systems.
- Clear understanding of; GMP, or any other GxP area, regulatory and accreditation systems, quality management, NC/CAPA, & Change Controls.
- Knowledge of legal framework concerning pharmaceutical manufacture i.e. Eudralex, ICH guidelines, medical device legislation.

**Apply**:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 55101 in all correspondence.

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