Quality Engineer

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!

 

Unternehmen: 
Unternehmen / Organisation: 
Randstad Professionals
Region: 
Neuenburg
Art der Anstellung: 
Temporär
Stellenprozent: 
100
Berufsfeld: 
Support, Management
Erforderliche Kenntnisse: 
Management