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 ?
Have you completed training/study/internship in Quality, Regulatory Affairs, post market surveillance, 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 specialist - someone who understands and can take on the complaints handling process within the company, 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, as such also the local language of choice, but with Business level English essential because complaints received are mostly in English and the parent company's corporate language also being English.
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 firstname.lastname@example.org together with scanned certifications of training and Arbeits Zeugnisse.
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, product recalls, FSCA, audit, regulatory, health authorities, distributor, notified body, Medical Device jobs, Nonstop recruitment, Manufacturing, Engineering
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