Regulatory Affairs Manager
Are you a professional in RAQM, searching for a new challenge?
Would you enjoy having the flexibility to delve into new topics and learn new skills, working in a global regulatory affairs position?
We are supporting our client, a leading manufacturer in the ophthalmic field, in their search for a Regulatory Affairs Manager for their site in Stuttgart.
Focuses:
Creation and further development of national and international regulatory strategies
Handling communication with Notified Body and authorities, as well as suppliers (win relation to approval procedures)
Supporting with the maintenance of the post-market surveillance system
Preparation and maintenance of risk analysis and technical documentation
Updating of SOPs
Supporting the Quality Management function
Experience required:
A degree in the medical/engineering field
2+ years of experience in Regulatory Affairs (within the healthcare/medical device sector)
Knowledge of regulatory requirements and medical device standards (e.g. ISO 13485 EU-MDR, ISO 14971)
Experience with the creation of technical documentation
Fluency in English and German
If you're interested in this position, please contact Hollie Dear for further details: hollie.dear@adaptivelifescience.com
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