
Quality Engineer - Medical Devices
- Twickenham, Greater London
- Permanent
- Full-time
- Quality Management – managing technical documentation, CAPA and writing/maintaining processes and procedures in compliance with ISO13485 QMS system. Verification and validation of ISO process and procedures.
- Management of the Technical Files.
- Risk Management File – maintenance and update of RMF in accordance with ISO14971.
- Active role in 3 new design projects including management of technical documentation in design process.
- Conduct internal audits and support external audits.
- Support on FDA registration for new products. Registration of products in different regions.
- Support the implementation and maintenance of the Post-Market Surveillance (PMS) system
- Collaborate with Purchasing to maintain a controlled list of approved critical suppliers, including risk classification.
- Degree in a Biomedical or Engineering-based discipline
- IT skills MS Office
- Must be fluent in written and spoken English to C1 level
- Good understanding of reporting requirements under MDR/ISO-13485
- Minimum 3 years working in a quality role at a medical device company.
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