Description
Contract Validation Engineer - Midlands
£40 - £50 DOE | Northampton| Contract/Interim
Contract Validation Engineer - Midlands - Global Pharmaceutical Company
Validation Engineer required for Pharmaceutical manufacturing site. Contract opportunity which will see you be responsible for ensuring changes and improvements made to manufacturing systems, storage and distribution and controls are executed in compliance with cGMP. Candidates must be eligible to work in the UK.
JOB TITLE
Validation Engineer/Quality Engineer/QA Engineer
LOCATION
UK/England/Midlands
LENGTH
12 Months
ROLE/DESCRIPTION
-Ensures all changes are managed within the change control process
-Responsible for ensuring change controls are executed to cGMP requirements
-Own the Validation master plan for the site facility
-Provides technical and expert quality compliance input into site validation strategy and protocol development
-Identify process control improvements and compliance risk improvements and works multi-functionally to deliver solutions
-Provides input to the specification, development and installation of process equipment from a regulatory compliance and quality perspective
-Provides expert input to process risk assessment and management
REQUIREMENTS
-Degree educated & Validation Engineering experience
-Ability to write protocol reports for validation or trial purposes
-Up to date knowledge of regulations
-Knowledge of drug or device regulations, including 21CFR Part 11/ISO13485
-GAMP5 knowledge