Position: Entry level

Job type: Full-time

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Job content

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).

Tasks
  • 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
Profile
  • 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!
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Deadline: 08-06-2024

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