Description
The ideal candidate would have experience working within these industries and candidates with academic experience in biomechanics, biochemistry or any similar medical discipline would be at an advantage. In depth knowledge of ISO and Medical Device Directive 93/42/EEC is essential.Experience required:
- Batch review and release
- CAPA
- Auditing
- Prepared and created CE Technical Files
- Worked to CGMP requirements
This is an exciting opportunity for anyone with the skill-sets described above to join an energetic and growing team of quality assurance specialists.
Please do forward this email to any friends or colleagues that may be looking. We offer £200 worth of vouchers if the candidate is placed successfully.
For a full job specification or if you would like to discuss the position in more detail please call Sarah Irvine on .