Senior Mechatronics Engineer

Abbott

Zürich

Vor Ort

CHF 90.000 - 120.000

Vollzeit

14 Tage+

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Zusammenfassung

Abbott is seeking a Sr. Mechatronics Engineer to join our team in Zurich, responsible for design updates and maintenance of medical devices. This role involves collaboration with engineering teams and managing regulatory aspects.

The ideal candidate will have a Bachelor's in Mechatronics or Electrical Engineering and 5+ years in a similar role in the MedTech industry, demonstrating strong skills in mechatronics, electronics, and problem-solving.

If you thrive in a service-oriented environment and have a maker mentality, apply today!

Qualifikationen

  • 5+ years of experience in a similar MedTech position.
  • Strong background in mechatronics and electronics.
  • Understanding of medical standards like IEC 60601 and ISO 13485.

Aufgaben

  • Lead and support On-Market products across regulatory and quality.
  • Manage multiple projects for timely completion.
  • Design, execute, and document tests per regulatory requirements.

Kenntnisse

Mechatronics
Electronics
Analytical problem-solving
Technical communication

Ausbildung

Bachelor's Degree in Mechatronics or Electrical Engineering

Tools

Windchill
Altium
Solid Works

Jobbeschreibung

Thoratec Switzerland GmbH is part of the medical device division of Abbott Laboratories, a fortune 500 company with over 115’000 employees worldwide. We are the global market leader for implantable and extracorporeal blood pumps based on magnetic levitation technology. Our life‑saving systems, which we develop and manufacture in Zurich, are used for advanced heart failure patients needing short‑ or long‑term circulatory support.

Our location in the heart of the city of Zurich has around 130 employees in the areas of development, quality and production of the CentriMag System and the HeartMate 3. We are looking for a motivated and talented.

Sr. Mechatronics Engineer

Join our team in Zurich. Become part of a young and aspiring team which is responsible for design updates and maintenance of mechatronic devices and consumables for our implantable and extracorporeal blood pump systems. With your work, you’ll ensure our products stay at the forefront of innovation and meet the highest standards of our industry. In your role you will be interfacing and collaborating with cross‑functional teams in Switzerland and the US.

Main Responsibilities
  • Lead and support On‑Market products with activities including manufacturing, regulatory and quality aspects for the entire portfolio, e.g. obsolescence projects, complaint investigations, corrective and preventive actions (CAPAs), regulatory and standard updates.
  • Manage multiple projects and tasks for timely completion.
  • For design changes, own and support Design Control Process documentation, e.g. risk management files.
  • Designing, planning, integration, execution and documentation of tests in compliance with Design Control process and regulatory requirements.
  • Work closely with Manufacturing Engineering and Production to sustain the electronics and mechanical parts of our portfolio.
  • Support Product development activities on the full life‑cycle of class 2 and class 3 Medical Devices.
  • Active participation in internal and external audits.
Required Qualifications
  • Bachelor's Degree in Mechatronics, Electrical Engineering or equivalent (ETH/FH or comparable education)
  • 5+ years of experience in a similar position in the MedTech industry
  • Strong background in mechatronics and electronics
  • Solid understanding of mechanics
  • Basic understanding on embedded Software architecture and documentation
  • Experience in Design Verification planning and execution
  • Knowledge of medical standards like IEC 60601, ISO 13485, FDA 21CFR820, ISO 14971, MDR, GMP, GDP
  • Excellent analytical and creative problem‑solving skills
  • Flexible collaborator with accurate working and documentation style
  • Strong technical communication skills and ability to collaborate with a cross‑functional project team (Manufacturing, Quality, Regulatory, etc.)
  • English Level C2 is required, communicative German is a plus
Preferred Qualifications
  • Hands‑on experience in electronics obsolescence activities
  • Knowledge of Windchill (PLM and Change Control system), Altium (PCB Design) and Solid Works (CAD)
  • Experience in manufacturing of mechatronic medical devices
  • Knowledge of statistical methods, techniques, and statistical software tools

We are looking for a service‑oriented person with a strong maker mentality who would like to be part of our enthusiastic team with broad responsibilities.

Do you have what it takes? Then send us your application including motivation letter, curriculum vitae, letter of recommendation and diplomas today. We are looking forward to meeting you in the heart of Zurich.

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