£100k - 140k per year + package
10 months ago
My client, a Medical Devices company are looking for a Regulatory Affairs Manager based in Switzerland.
A great opportunity to join a fast-growing company with a great portfolio of products.
Regulatory Affairs Manager
Salary: Up to 140,000 CHF
Global Medical devices company
- Supporting of international registration submissions
- Ensuring that regulatory requirements for the approval of medical devices are met during the product development process
- Supporting in the preparation and execution of audits
- Communicating of new regulatory approval requirements
- Participating in the respective product development teams
To be considered you need to have
- Eligibility to work in Switzerland
- 3+ years’ experience in global regulatory affairs experience
- MDD experience - Mandatory
- English fluent - Mandatory
- MDR experience - Desirable
- German fluent - Desirable
I will also look for an RA manager and QA/RA manager in different German location
Looking but this isn’t the right position for you?
If you are interested in a new opportunity but your experience doesn't fit this role, please email your CV to email@example.com
Or callDE: +49 (0) 69 94189255
for a confidential discussion about potential opportunities.
NOT OF INTEREST TO YOU BUT KNOW SOMEONE IT WOULD BE?
CLS offer a generous referral scheme reward, whereby anyone who refers us to a successfully placed candidate is entitled to up to £250 worth of vouchers.
Catalyst Life Sciences
CLS are a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets.
- Pre-clinical Development & Safety
- Clinical Development
- Medical Affairs & Information
- Regulatory Affairs
- Pharmacovigilance/Drug Safety
- Quality & Validation
My Linked In Profile
I personally specialise in recruiting QA, RA and validation professionals for roles across DACH so please do get in touch should you be considering new roles or looking to fill ones at your current company!
RA / regulatory / MDD / MDR / devices / 13485 / submission / regulatory / FDA / CFR / 21