Packaging Device Engineer
Altran
Basel, CH
vor 1 Tg.

Our offer

  • A permanent contract with the leader in innovation and high-tech engineering consulting
  • A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR.
  • 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D).

  • In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
  • Altran deploys its expertise particularly in : Life Sciences (Pharma, Biotech, and Medical Devices), Industry, Aerospace, Automotive, Energy, Railways, Financial Services : P&C Insurance, Health Insurance, Reinsurance, Banking Telecoms Public sector
  • Your role

  • Leading the definition of product requirements for packaging, medical devices, delivery systems, e.g. drug / device combination products in which the device is generally already registered but sometimes to be developed
  • Provide primary packaging and device expertise in a broader cross-functional drug product development team
  • Supporting and coordinating the manufacturing of clinical material and the production scale up
  • Managing and monitoring Human Factors Engineering activities
  • Leading Risk management activities
  • Planning and monitoring of design verification activities (in-house)
  • Ensuring a high quality Design History file
  • Your profile

  • MSc degree in Packaging Science / Engineering
  • An ideal candidate would have a relevant degree in engineering and at least 7 years’ experience in leading device development technical teams in a similar area
  • Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation)
  • Development and writing of technical documentation of drug / device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects
  • Experience with Design Control, ISO1345, Primary Pharmaceutical Packaging Development, ideally for combination products is important.
  • Fluent in English and German is clearly a plus
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