Location: Central Belt, Scotland, United Kingdom
Salary: No information
Sectors: Life Sciences
Job Type: Contract
Apply for this Job

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.

Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.

To find out more about Huxley Engineering, please visit

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

Apply for this Job