Do you have at least 2 years of quality engineering experience ? Do you want to continue your development in the medical device industry ? You should then read the following lines!
One of our clients, specialized in medical devices and based 30 minutes away from Neuchâtel, is looking for a Quality Engineer for a duration of 1 year (high possibility of extension).
Quality support for production and for various projects
Plan, coordinate and direct the quality aspects of process validation
Write validation documentation (protocols, reports, process specifications, work instructions, pFMEA, master validation plan)
Provide projects updates and presentations
Review and approve changes to documentation and processes
Apply and enforce GMP
Non-conformance management (initiation / evaluation / disposition on the batches / investigation)
Quality control technical support
Participation in development and updating of procedures and other quality documents
Participation in validations of new processes (Processes, products, methods & software)
Validation of different integrated processes
Minimum of 2 years' experience in Quality Engineering area (Medical device or pharma industry experience highly preferable)
Engineering degree or equivalent
Knowledge in statistic (capability, gage RR, Anova test, control chart)
Quality knowledge in the medical industry
Fluent in French and english
Ability to work with cross functional team (R&D, RA, manufacturing engineering, planning, production)
Do those lines sound familiar ? Do not waste a second and apply now!
Randstad (Schweiz) AG