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 SUPPLY CHAIN

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 - URGENT - Med Dev - German/English - Zurich

This is a small production site local to Zurich but within a large international company supplying to Medical devices and biopharmaceutical industries, and growing. An opening has just arisen within their Swiss site for a Quality Engineer - this is a permanent position with good career development prospects and an ASAP start, although longer notice periods will also be considered.

The role itself is broad and is likely to include Complaints handling and tracking (English and German both needed), risk analysis, equipment qualification, QC, non-conformance evaluation, change management, documentation, and supporting production related process improvement.

Staff within the company come from varied backgrounds including Engineering, Quality management, Plastics, Medical devices and Pharmaceutical. A minimum of 3 years industry experience within a tightly regulated sector is sought but preferably ISO 13485 or GMP would suit, and ideally with a good knowledge of risk analysis and FMEA, 8D problem solving, SPC, MSA, and Lean Six Sigma. German and English are both needed.

As the company is growing, this role is open to a more junior person looking to learn and develop their QA skills (No graduates please), while Quality professionals wanting to take on leadership duties longer term are also welcome to apply.

If this role sounds like a good match please do apply to the Senior Consultant Andrew Boroky on 0041 43 50 80 817, 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
Jul 31, 2020

Contact info

NonStop Consulting
Andrew Boroky
p0w yw y- z7 )y( 07g
Not available