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Job Details
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Complaints specialist - Swiss MedTech - English/German

Business Type: Clinical Research Organisation, Laboratory, Medical Devices Company, Other Business, Contract Manufacturing
Job Type: Medical Devices, Manufacturing - Production, Quality Assurance - Control, Regulatory Affairs, Compliance
Job Level: Experienced (non manager)
Position: Full Time
Location: Switzerland
Reference: AB-65177-5
Closing Date: 01/08/21
Job Details:

Complaints specialist - Swiss MedTech - English essential, German beneficial - permanent position

Are you looking for a step into the industry but don''t have the experience ?

Do you have an engineering background, and completed training/study/internship in Quality, Regulatory Affairs, post market surveillance, or clinical that would prepare you for a career in Complaints handling and product quality ?

Our client is a globally active medical devices manufacturer in a leading market position and growing. On top of their ''wanted'' list is a Complaints specialist - someone who understands and can take on the complaints handling process within the company, involve themselves in inspection of returned devices, while at the same time updating and escalating Post Market Surveillance data, and supporting the Quality department in broader tasks relating to failure mode analysis, recommended corrective actions, and compliance to Quality regulations internationally (ISO 13485, MDR, GMP).

Our client is located in the German speaking area of Switzerland - Business level English is essential because complaints received are mostly in English and the parent company''s corporate language also being English. Given the location, German is naturally beneficial

This is a key role for the company, and interviews will be arranged at short notice, so please apply now.

For more information on this vacancy, or any other QA opportunities within the Swiss Medical Devices sector, please contact the Senior Consultant Andrew Boroky on 0041 43 50 80 817, or email him at together with scanned certifications of training and Arbeits Zeugnisse.

KEY WORDS: Vigilance, adverse event, incident, root cause analysis, post market surveillance, Complaints, Switzerland, Quality Assurance, quality engineer, junior, graduate, Compliance, CAPA, Medical Devices, English, 21 CFR 820, MDR, ISO 13485, product recalls, FSCA, audit, regulatory, health authorities, distributor, notified body, Medical Device jobs, Nonstop recruitment, Manufacturing, Engineering

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

Posted: 25/07/2021 | NPJ Ref: 276249
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