Mechatronic Engineer (m/w)
Cytiva
Eysins, Switzerland
vor 5 Tg.

Help us improve access to life-changing therapies that can transform human health

We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics.

Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.

Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies.

Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

What you'll do

We are looking for a Mechatronic Engineer who will be working in Eysins (Nyon) in Switzerland and be part of a multidisciplinary R&D team developing medical devices and manufacturing equipment aiming to process biological cells in the field of blood transplantation and cellular therapies.

The Mechatronic Engineer will be responsible for improving the existing equipment product portfolio, involving mechanical and electronical activities, and supporting a growing manufacturing product line from a technical perspective working with multiple stakeholders internally and work closely with external suppliers.

  • Generate ideation around product improvement of existing equipment and perform technical feasibility studies in collaboration with a R&D multidisciplinary group.
  • Assess project specifications or change controls for improving the robustness, usability or the manufacturing of existing devices.
  • Write project technical specifications, execute development and perform verification and validation activities with focus on quality, compliance and execution rigor.
  • Work in close collaboration with R&D team members, suppliers, Production, Supply Chain, Quality and product management.
  • Mitigate project technical risks, resolve issues, deliver on-time and communicate effectively
  • Ensure compliance with ISO13485 or ISO9001 standards and other QMS requirements
  • Who you are

  • University degree or equivalent in related scientific or engineering fields (physics, mechatronics, electronics or similar)
  • 5+ years of a successful experience in new product development, product care, project management and manufacturing equipment, ideally for the medical or life science industry involving cross-functional teams.
  • Demonstrated first experience in improving, developing or manufacturing multidisciplinary equipment platforms involving mechanics, electronics or low-level firmware needs.
  • Demonstrated ability to clearly communicate (oral, written) across global, cross-cultural, cross-functional teams and stakeholders
  • Founded knowledge and practical experience of the product lifecycle and relevant know-how about regulations such as ISO 9001, ISO13485, cGMP, specifically for the US and European market
  • Fluent in English, second language a plus
  • Result driven, autonomous at work, creative, initiatives welcomed
  • Who we are

    Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here.

    If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.

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