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Complaints coordinator, PMS - Swiss MedTech - English essential

Business Type: Pharmaceutical Company, Clinical Research Organisation, European Public Health Authority, Medical Devices Company, Other Business
Job Type: Medical Devices, Quality Assurance - Control, Clinical Operations, Pharmacovigilance, Compliance
Job Level: Experienced (non manager)
Position: Full Time
Salary: Up to CHF80000 per annum
Location: Switzerland
Reference: AB-62205-1
Closing Date: 19/08/19
Job Details:

Urgent - Complaints coordinator - Swiss MedTech - English essential

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

Have you completed training/study/internship in Quality, Regulatory Affairs, post market surveillance, laboratory assistant or clinical that would you 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 Officer - someone who understands and can take on the complaints handling process within the company, while at the same time supporting the Quality department in broader tasks relating to growth of the Quality Department and compliance to Quality regulations internationally. These will include CAPA / NC identification, internal and external supplier audits, documentation creation/review, training materials, data analysis and process improvements.

Our client is located in the German speaking area of Switzerland. German is naturally beneficial due to this location, nevertheless English is essential as it is the company and internal language of choice. This is a key role within the Quality department - 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 80 816, or email him at together with scanned certifications of training and Arbeits Zeugnisse.

For industry news and new opportunities in QA within the Medical Devices and Diagnostics sectors, please join my Linked group at

KEY WORDS: Vigilance, adverse event, incident, post market surveillance, Complaints, Switzerland, Quality Assurance, Compliance, CAPA, Medical Devices, English, 21 CFR 820, MDR, MDD, ISO 13485 / IEC 60601, 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: 12/08/2019 | NPJ Ref: 240150