Validation Manager - Great Yarmouth, United Kingdom - CK GROUP

CK GROUP
CK GROUP
Verified Company
Great Yarmouth, United Kingdom

2 weeks ago

Tom O´Connor

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Tom O´Connor

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Description

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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