Sterile QAV Engineer

Description

My global market leading pharmaceutical client based on the South Coast of the UK is currently seeking a QAV Engineer

My client is running a number of high value projects concurrently with a combined value of circa £200M. They require QAV specialists to work on the projects and can offer a long term opportunity, paying attractive hourly rates in a great location.

Responsibilities:
•Develop/Review/Approve Validation Plans.
•Implement, deploy and revise as applicable Validation procedures.
•Review / Approval of Validation Protocols ( e.g. URS, Facility, Utility, Process, Cleaning, Test Method, and Equipment validations) to ensure compliance with current regulatory expectations, EU,FDA and Corporate Standards and Internal Procedures
•Review / Approval of Validation Reports ( e.g. URS, Facility, Utility, Process, Cleaning, Test Method, and Equipment validations) to ensure compliance with current regulatory expectations, EU,FDA and Corporate Standards and Internal Procedures.
•Ensures that change requests and Document Change Requests are compliant with all applicable procedures.

Education and experience:
•Minimum of degree qualification in relevant science and/or engineering discipline
•3 Years minimum post educational experience with working in a regulated environment preferably within a Pharma/Biotech facility