Requirements

Required education level
Ad. Federal PET / Fed. PET Diploma, Bachelor, Master
Required experience
Between 1 and 3 years
Required language knowledge
English German
Required skills
Compliance supply chain Regulatory English Medical Devices Switzerland Supply Chain MEDICAL DEVICES SWITZERLAND Supply chain compliance medical devices switzerland english Medical devices quality assurance ISO 13485 Audit CAPA validation 21 CFR 820 Switzerland Quality Assurance complaints Validation ENGLISH Quality management Quality Management audit REGULATORY Quality assurance MDD german quality management regulatory MDR QUALITY ASSURANCE Audit COMPLIANCE German Complaints

Details

Location
Other countries
Term of employment
Full time
Sector
Medical technology
Professions
CNC / Machine operator Design / CAD / CAM Quality Control / Processes Management / Project Managemen... Electronics / Electrotechnical Alternative / Renewable energy Environment / Safety Engineer / R & D Mechanic (Precision / Micro /... Car Mechanic / Car Electrician... Preparatory Work / Production Manual Worker / Qualified Manu... After-Sales Service / Maintena... Speciality of Watchmaking Technical-commercial Business- / Requirement Analys... Consulting / Management / Proj... SAP Project Management / Consu... Data Warehouse / Business Inte... Software Development / Softwar... Web Development / Publishing /... ERP (Oracle, Sage, Infor, Micr... Helpdesk / Support / Training Networks / Security / Hardware Database specialist / Architec... SAP Basis / Module Specialist System Technician / - Administ... Testing / Audit / Release Mana...

Description

Quality Engineer - Electronic Med Dev products - strong growth forecast - German/English a MUST

Our client is a specialist manufacturer of miniature electronics products for the Medical Devices sector. Due to internal reorganisation, a new position as Quality Engineer has become available to start ASAP with the organisation based in German speaking Switzerland.

Duties will be broad, in providing Quality support to a number of departments (Medical device and non medical device related products), ensuring compliance to internal, as well as external quality standards ISO 9001, ISO 13485 and EN 9100. Internal and customer audits form an important part of the role, as is complaint management, CAPAs, document management, and training.

Essential requirements of this role are a technical or scientific background, with some industry experience working with ISO 9000 and/or ISO 13485, and German and English language skills (all process documentation is in German). Programming ability in Python and a knowledge of statistics are both an advantage, while previous experience working with electronics could also be utilised.

The company is growing across multiple divisions. The reorganisation means they are also growing their quality department and looking for flexibility they are considering both junior and more senior Quality engineers. Initial interviews will be organised within a week, so if this is role sounds like a good match please do apply to the Senior Consultant Andrew Boroky on 0041 43 50 80 816, and email him at a.boroky@nonstopconsulting.com ahead of a confidential discussion of this opportunity.

KEY WORDS: Quality Assurance, QA, Compliance, Auditor, Medical Devices, Switzerland, ISO 13485, ISO 9001, ISO 14971, GMP, CAPA, Corrective action, design control, SPC, QSR, preventative action, Production, Manufacturing, Medical Device jobs, nonstop recruitment

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 Consulting
Feb 11, 2020

Contact info

NonStop Consulting
Andrew Boroky
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Not available