Description
Clinical Evaluation Specialist (m/f)Our client, an international company based in the Zurich area, is looking for YOU as a Clinical Evaluation Specialist (m/f).
Your tasks
- Writing of Clinical Evaluation Plans and Reports according to current European Medical Device Regulations
- Reviewing, structuring and revising existing Medical Device Clinical Evaluation Documents (Life Cycle Management)
- Systematic literature searches in appropriate data bases and documentation
- Proactive cooperation with other departments in the company to ensure smooth clinical evaluation process of medical devices
- Enforce compliance to regulations and internal processes to adhere to the new Medical Device Regulations (MDR) standards
- Transferring of knowledge on Medical Device Regulations standards documentation into organization
Your profile
- PhD in a Bio-Scientific or Medical discipline (e.g. Biochemistry, Biomedical Degree, Dentistry Degree), incl. professional experience in systematic literature searching
- About 3 years of experience in a similar position in a professional environment
- Excellent written and verbal communication skills in English
- Excellent command of MS Office applications
- Previous experience in Medical device industry
- Previous experience in Medical writing with RA or clinical evaluation background
- You are a communicative, agile team player as well as a structured and goal-oriented person
Key facts
Start date: as soon as possible
Location: Zurich area
Workload: 100 %, negotiable
Home Office: negotiable
If you are interested in discussing further details about this or similar positions, kindly contact me as soon as possible!
Best Regards
Elena Reeb
Recruitment Consultant Medical Devices
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Sthree Switzerland is acting as an Employment Business in relation to this vacancy.