Description
Duties:- Working on a project for device assessments for all systems site wide.
- Working across filling, packaging and assembly areas.
- Reviewing equipment on site and identifying and resolving issues.
- Producing documentation to GMP and regulatory standards.
- Previous experience in the Pharmaceutical industry.
- Engineering/Validation/Process background.
- Excellent communication skills (verbal and written).
- Ability to cope with fast moving tasks and a quality driven focus.