Beschreibung
Product Development Engineer - Medical Devices
Are you a Product Development Engineer within experience in a medical devices environment and looking for an exciting new opportunity with a market leading global company?
If so, please have a look at the following details
On behalf of our client, an international company specialized in medical devices based in Solothurn area, we are looking for a Junior Regulatory Affairs Specialist within experience in medical devices. This is a challenging contracting position starting in July until the end of the year.
Your responsibilities:
As a Product Development Engineer you will be responsible of:
- The maintenance of existing implants and instruments
- The maintenance of existing Technical File and Design History File documentation
- Write Standard Evaluation EN ISO 14630:2012 and EN ISO 14602:2011
- Write Design and Clinical Risk Management
- Information exchange and collaboration between internal, local, external and foreign partners
- Preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL)
To deliver the best output, it's needed that you have:
- A degree in engineering
- Experience in a regulated industry
- Excellent communication skills in English and strong leadership ability
- German will be a plus
If you are a dynamic and motivated Product Development Engineer currently looking for a challenging new position that applies to your skills, then we look forward to receiving your application!
Don't hesitate and send us your CV today through the link in the advert. In case of any questions please contact Julie Mackerer.
Experis IT is Europe's leading IT&T recruitment agency.