Vývojový inženýr

Would you like to work in medical industry? Do you want to be responsible for projects related to the design and manufacture of medical devices? 

We are looking for a reliable collegue who will focuse on the removal of hazardous substances as defined by EU/MDR 2017/745 and compliance of the Business Unit CE marked medical devices to the new MDR and revised ISO standards.

Main responsibilities

  • Lead projects in the redesign or replacement of materials defined as hazardous.
  • Interface with Suppliers, Procurement function, Quality and Regulatory Affairs to deliver projects.
  • Plan and lead the verification and validation activities for new/replacement of materials.
  • Interface with suppliers to obtain quotations, purchase components, and debug problems with replacement parts.
  • Interface with relevant Functions to obtain device samples for testing. 
  • Implement the product-level material change plans related to satisfying product design specifications, verification and validation activities including product performance, biocompatibility validations and usability studies or evaluations. 
  • Coordinate and implement laboratory testing, data analysis and preparation of technical reports.
  • Collaborate with the required internal process experts and process engineering and Quality and Regulatory teams to execute the new material implementation.

What we offer?

  • Strong independence and responsibility in the entrusted area 
  • Professional team 
  • Career opportunities within Teleflex 
  • All relevant training and coaching for your continuous professional growth 
  • Attractive salary 
  • Interesting benefits including flexible hours and home office 
  • Modern working location 

Naše benefity

Týden dovolené

Dotované závodní

Čisté pracovní

Příspěvek na

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