QA Resources are looking for a number of contract CQV Engineers for an exciting project based in Cork.
Role and requirements:
- Support and participate in the design of systems and equipment to ensure they comply with cGMP requirements.
- Preparation and execution C&Q protocols as required (e.g. URS’s / SRS’s, Plans, Impact Assessments, DQ, IQ, OQ, PQ protocols and Reports).
- Review and approve documents prepared by contractor organisations (e.g. vendor SAT’s, FAT’s, commissioning protocols, project change controls/notifications).
- C&Q System / Equipment / Components as per site procedures.
Education and Experience:
- Third level degree in Engineering or Science and relevant experience.
- Minimum of 2+ years’ experience in the pharmaceutical industry with excellent working knowledge of cGMP
- Experience of commissioning, qualification and validation of any of Process, Equipment and /or Utilities
Interested candidates should submit an updated CV to enquiries@qaresources.com
To apply for this job email your details to enquiries@qaresources.com.