Quality Engineer for MDR Validation

SolothurnTemporaryChemistry, Pharma, Biotech2019-05-15Bachelor / University of Applied Sciences
For our client, we are currently looking for a Quality Engineer for MDR Validation projects.

Quality Engineer for MDR Validation

Your challenges

  • Liaise with key stakeholders to meet project plan
  • Collaborate with suppliers to obtain details for manufacturing process inoformation, production risk management and direct part marking
  • Ensure extarnally manufactured products meet EU Medical Devices Regulation requirements
  • Assess supplier drawingsand process information to support project deliverables
  • Resolve issues with obtaining Supplier Product information
  • Support Review and Approval of supplier Process Validation Protocols and Reports as applicable
  • Support the update of supplier related inspection criteria


Your skills

  • Bachelor Degree in Engineering or associatedd technical field
  • Minimum 3 years experience in Quality Engineering and 2 years within Medical Devices or Pharma industry
  • Good knowledge of ISO 13485 and FDA QSR
  • Fluency in GERMAN and English are a must for this role


Your contact

Frau Tanja Vrbanic, Recruitment Consultant, looks forward to answer your questions by phone +41 58 233 2100.

You can apply directly online.

Apply