Livingston, West Lothian
about 1 year ago
Reporting to the QA Manager this role is responsible for providing administrative support to the QA Department. The ideal candidate will therefore have a background in Quality assurance within a scientific environment.
Key responsibilities and accountabilities:
Support to the site QMS.
Review of SOP's.
Review, approval and issue of laboratory documentation.
Control and maintenance of GMP documentation.
Implementation, routine review and approval of change controls.
Involvement with investigations arising from deviations.
Assist with both internal and external audits and follow up of actions arising from them as required.
Support the supplier assessment program.
The ideal candidate will be:
Results oriented with a positive outlook and clear focus on high quality output.
Able to demonstrate good written and verbal communication skills.
Able to get on with others and be a team player, but be equally comfortable working independently.
Attention to detail.
Comfortable dealing with senior managers, external auditors and suppliers.
Willing to learn from others.
Experience of working in a similar role within a GMP environment
Experience of document review and control.
Able to communicate effectively with people at all levels
Able to write clear, concise reports.
A degree or equivalent in Chemistry, Pharmacy, Biology or general science.
Must be competent in generating documents and writing reports both for internal use and for customers/clients. Must be numerate.