Requirements

Required education level
Compulsory education, CFC/EFZ, Bac. / Federal Vocational Bac.
Required experience
Between 1 and 3 years
Required language knowledge
English German
Required skills
Compliance Regulatory English Medical Devices Switzerland MEDICAL DEVICES SWITZERLAND compliance post market surveillance medical devices switzerland english Medical devices quality assurance Audit CAPA 21 CFR 820 Switzerland Quality Assurance ENGLISH Complaints audit REGULATORY complaints Quality assurance MDD german regulatory product recalls MDR QUALITY ASSURANCE Audit COMPLIANCE Vigilance adverse event incident German ISO 13485 / IEC 60601 FSCA

Details

Location
Other countries
Term of employment
Full time
Sector
Biotechnology / chemistry / ph...
Professions
Reception / Secretarial Public Administration Assistant / Executive Assistan... Administration clerk / process... Office Manager

Description

Urgent - Complaints coordinator, Adverse event reporting - 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, or clinical that would you prepare you for a career in post market surveillance and vigilance reporting ?

Our client is a globally active medical devices manufacturer - in a leading market position and growing. On top of their 'wanted' list is a junior Vigilance specialist - someone who is motivated to work in this area, who understands post market surveillance in the Medical Devices industry, and with training, can take on the key role of addressing complaint and vigilance reporting processes, and ultimately in prioritising, resolving, and reducing the complaints themselves. They will similarly become the main contact with health care providers and regulatory agencies to ensure all questions are addressed within established time-frames.

We are aiming for June/July start date ideally, 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 quality@nonstop-devices.com 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 ch.linkedin.com/in/qaswitzerland/en

KEY WORDS: Vigilance, adverse event, incident, post market surveillance, Complaints, Switzerland, Quality Assurance, Compliance, CAPA, Medical Devices, German, 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.

NonStop Recruitment
Not available

Contact info

NonStop Recruitment
Andrew Boroky
10w yw y- z7 )y( 07g
Not available