Description
A leading bio-pharmaceutical organisation with operations in the US, Germany and Australia is looking for an experienced Validation Specialist to support their UK based manufacturing facility.As part of the Validation Group and supporting an ongoing investment programme, you will be involved in the qualification of formulation and aseptic fill/finish equipment.
The role will include a combination of Protocol (IQ/OQ/PQ) and Documentation generation as well as hands on execution.
This opportunity would suite a multi-disciplined Validation Engineer.
Skills/Experience required:
- Experience of working on either formulation or aseptic Fill/Finish equipment such as: fluid harvesters, centrifuges, vial, syringe fill/finish lines.
- Working knowledge of IQ/OQ/PQ protocol generation and execution.
- Conversant in cGMP and Engineering Guideline.