Regulatory Affairs Manager - Medical Devices
Job Details
A pioneering Medical Devices company, located in Switzerland is currently looking to bring in a Regulatory Affairs Manager to join their Swiss HQ on a permanent basis. This is a full time role and would suit somebody who has a strong background in Regulatory Affairs, with a combination of drug and device experience, along with management experience.
Role:
- Providing advice and support to project teams and management relating to regulatory matters.
- Be part of a team responsible for innovative products and variation projects, with a focus on the regulatory and labelling aspects.
- Support other Regulatory Managers across the globe with combination product submissions.
- Form and maintain relationships with regulatory agencies.
Qualifications:
- Life Sciences degree or equivalent.
- Strong experience in Regulatory Affairs in a medical device setting, with experience of combination drug/device products.
- Good negotiation skills along with good communication skills.
- Good understanding of Regulatory procedures and guidelines relating to Medical Devices.
To Apply:
Please click on the apply button. Ideally, please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty applying or if you have any questions, please call me (Tim Seydali) directly on +44 (0)207 4400 673 or upload your CV on our website: www.proclinical.co.uk
Full job descriptions are available on request. Please note that not all of our vacancies are advertised. To register as a priority candidate, please upload your CV on our website with a short description of what you are looking for or call 0800 988 4437. We will then contact you with relevant roles. We regard all correspondence as confidential. Thank you.
ProClinical is a specialist Employment Agency and Recruitment Business, providing employment opportunities with major companies in the Pharmaceutical and Biopharmaceutical industries across Europe.
