Quality & Regulatory Affairs Assistant in medical devices field

headquarter Polydentia
Mezzovico-Vira, 6802, Switzerland
Quality & Regulatory Affairs assistant in medical devices field 100%

job description

Polydentia SA is seeking for a Junior Quality & Regulatory Affairs in medical devices field who will support the Quality and Regulatory Affairs Manager in the certification processes EN ISO 13485:2016 and CE marking.

qualifications

• Biomedical Bachelor Degree
• Minimum 2-3 years of experience in the quality and regulatory competence sector, preferably in the dental sector
• In-depth knowledge of the EN ISO 13485:2016 standard, of the European directive on medical devices 93/42/EEC and on the new European regulation MDR 2017/745
• fluency in Italian and English

desired skills

• Motivation, interpersonal effectiveness, oral and written communication proficiency, organizational skills (prioritization, project management)
• Ability to work in team
• Analytical and problem-solving skills
• Excellent computer skills

location

Mezzovico-Vira, Switzerland

apply now

If you believe you are the right person, you can send your application to Mrs. Federica Tessari, HR Manager at the following e-mail address: f.tessari@polydentia.ch