- NyonPermanent
Our client is looking for a Technical Documentation Coordinator to support its regulatory affairs team.
Great opportunity to join a market leader in medical device
To support the regulatory affairs team
- ZürichPermanent
Within this function as Verification and Validation Manager you`re responsible for the effective planning and execution of all verification and validation activities within the organization.Innovative company in the field of Medical Devices
Versatile function within a dynamic environment
- ZürichTemporary
In this function you'll manage all tasks related to the verification and validation activities of software, processes, products, equipment etc.
Dynamic Medical Device organization
Immediate availability required
- ZugPermanent
Support the Global Regulatory Team
Be an expert and guide Promotion and Advertising Regulatory affairsJoin a leading global medical devices player
Be a key member of the Regulatory Affairs team
- ZugPermanent
This role is for a Quality and Regulatory Affairs specialist to oversee our clients Legal Manufacturing activities.
Quality and Regulatory Management Representative
Point of contact for Notified Bodies
- ZugTemporary
Manage FSCA in a global Medical Device organization
Immediate availability required
Global MedTech organization
- ZugTemporary
Challenging opportunity with focus on MDSAP and MDR.
Immediate availability required
6-months assignment
- GenevaPermanent
We are looking for an Education Manager specialized in the orthopaedic industry.
Key Operational Role
Orthopaedic Industry
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