Regulatory Affairs Manager-Growing Company-Medical Devices-CH
A fantastic management role has come in within the canton of Bern for a regulatory affairs manager. This is a great time to be joining our client's regulatory affairs department as they are at an exciting point of growth; allowing you to be part of the future! We want to hear from you today if you have several years of experience within regulatory affairs from the medical device industry. Apply now to find out more about this great role!
As the regulatory affairs manager in this role your responsibilities will include but will not be limited to:
- Working on technical documentation and registration process of class I through to class III devices.
- Work closely with the quality department, with specific attention to QMS.
- Manage the international registration process of innovative medical devices.
The ideal candidate for this role will have several years of experience within regulatory affairs from the medical device industry. You will have worked on the full product life cycle of class I through to class III medical devices. You will have good working knowledge of ISO 13485. You will be fluent in both English and French.
Apply now to find out more about this fantastic opportunity to join a growing medical device company within this regulatory affairs manger role.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on email@example.com or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.
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