Our client is a privately-owned global leader in Ophthalmic medical devices. Due to product expansion, growth in new markets and the new European regulations, they are looking to strengthen their team with a QA/RA Manager. This position will work closely with the Head of R&D and the CEO, offering a collaborative culture and an innovative working environment.
- Ensures that procedures and processes are maintained and updated to be consistent with regulatory changes including the development of more efficient QMS processes
- You review and approve device related development documentation by overseeing the design control process and the whole device related life cycle process
- Participation in and performance of internal and external audits
- Working to ISO 13485
- Manage the verification and validation of the company software products and systems according to internal software lifecycle management processes
- 3-5 years of RA/QM experience at a Medical Device company (Ideally with expertise in Ophthalmic Devices)
- Academic technical background, or from a Quality Engineering position
- Weighted focus on quality management systems to ISO 13485
- Experience in the MDD/MDR transition for Europe
Please apply with your CV or contact the job poster Rebecca Stevens for further details on this opportunity and additional vacancies in Regulatory Affairs and Quality Management.
+44 208 638 5376