Validations Specialist Job in South Wales, Wales UK

Key Requirements

• Experience and a thorough knowledge of the Validation life cycle.
• Degree educated in Chemistry, Pharmacy, Microbiology or allied sciences.
• Experienced in completing PQRs.
• Experience in investigational (clinical trial) and marketed (commercial) products.
• Excellent communication and interpersonal skills
• Able to self manage, multi-task and be self motivated.

Key Responsibilities

• Ensure the complete delivery of fully compliant Product Quality Review reports and any follow up actions.
• Responsible for the preparation, review and approval of validation master plans and validation plans.
• Preparation, execution, review and approval of qualification and/validation documentation in relation to instrument, equipment and utilities.
• The review and approval of third party generated protocols and reports along with the review and execution and approval of factory acceptance tests and site acceptance testing activities.

In summary the successful candidate will have good validation experience and a good understanding of GAMP and CSV.