Quality and Validation Officer

Michael Page Engineering & Manufacturing
£35,000 per annum
16 Feb 2018
23 Feb 2018
You will support improvement to quality and validation systems; streamline processes. Identify risk areas and required mitigation to meet regulatory inspections. You will be play a key role in the Quality team. Client Details My client is global organisation with multiple sites through out the UK. They have major growth and expansion plans for 2018 and have extremely long retention of personnel due to the positive culture they foster and encourage. Description Key responsibilities will be to: Work as a key member of the Quality team Ensure that the Site Validation Master Plan is maintained accurately and Validation Plans are implemented. Author or review and approve the development and implementation of Validation Plans Technical input into all Validation Life cycle activities as part of a cross functional team. Schedule and coordinate the review of process and equipment validation and re-validation. Serve as subject matter expert and/or team member to support Quality Investigations. Contribute to and perform related training on site with regards to validation life cycle and compliance. Prepare and present validation reports and Key Performance Indicators for management review. Provide support in achieving / maintaining compliance with 21 CFR Part 11 / EU GMP Annex 11. Profile The successful candidate will have Validation, Quality or Technical experience and expertise within the Pharmaceutical, Medical Device or Biotechnology industry. Job Offer £35,000-£37,000 plus a generous performance bonus and benefits package.