Quality Engineer 70% - flexible hours - Life Sciences
Quality Operations Engineer - part time - flexible working hours - Swiss MedTech with German and English both needed
Good solid hands on quality work with responsibility for quality and compliance in production. That means logging and recording of deviations/complaints in the production process, prioritising problem areas, and organising and implementing necessary corrective measures. Ensuring appropriate documentation for the above tasks and liaising with Global Complaint Unit and Regulatory Affairs to ensure process compliance.
Typically we'd expect 3-5 years previous experience working in quality in a tightly regulated environment, ideally using ISO 13485, ISO 9001, ISO 19011, and FDA regulations. Business level German and English are both required.
The position is 70% of fulltime, and with flexible working hours. Within easy reach of Zurich via public transport and auto, ours is an international client with a long history manufacturing products for the Life Sciences markets, excellent history wrt audits, and after recent acquistion verymuch in a growth phase.
For industry news and new opportunities in QA within the Medical Devices & Diagnostics sectors, please also join my Linked group ch.linkedin.com/in/qaswitzerland/en
KEY WORDS: Quality Assurance, QA, Compliance, Auditor, Validation, MSA, Test Method Validation, Medical Devices, Switzerland, ISO 13485, ISO 9001, ISO 14971, GMP, CAPA, Supplier Quality, Corrective action, 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.
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