My client are a specialised contract manufacturer within pharmaceuticals. The role is an initial 6 month contract.
Site presence is required.
QA Validation consultant with previous experience working on electronic batch record review and material release, ensuring compliance with GMP requirements as well as deviation review and approval.
Providing validation support around the auditing of equipment validation.
Assist in the preparation for regulatory and customer GMP inspections.
Perform GMP audits on site.
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To find out more about Huxley Engineering, please visit www.huxleyengineering.com
Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales