MedTech Robotics Manufacturing Engineer — 60% Travel

Distalmotion SA

Épalinges

Vor Ort

CHF 110.000 - 150.000

Vollzeit

Vor 10 Tagen
Bewerbungsgenerator

Eine maßgeschneiderte Bewerbung für diese Stelle — ein maßgeschneiderter Lebenslauf und ein Anschreiben, die genau zur Stellenanzeige passen.

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Zusammenfassung

Distalmotion SA seeks a Robotics Manufacturing Engineer to drive industrialization and manufacturing engineering for the Dexter surgical robot and its accessories. You will own sustaining engineering, manufacturing testing, RCAs, and design transfer in a regulated ISO 13485 environment at the CMO site.

You will collaborate across functions to support ramp-up, perform root-cause analysis, and lead change-control activities while ensuring documentation and QMS compliance.

Qualifikationen

  • MSc or BSc in mechanical or mechatronics engineering.
  • 3-6 years in medical device manufacturing (Class II).
  • Hands-on experience with complex electromechanical assemblies in production.
  • Working knowledge of ISO 13485 and change-control execution.

Aufgaben

  • Act as the manufacturing link between CMO, supply chain, quality and R&D HQ, supporting ramp-up.
  • Perform level-2 production troubleshooting and mechanical root-cause analysis on electromechanical assemblies.
  • Initiate and execute Change Requests and Design Transfers in the QMS, assess impacts on tech and quality.
  • Edit SolidWorks drawings, assemblies and BOMs for manufacturing changes and submit rev-ups for R&D review.

Kenntnisse

Mechanical engineering
Regulatory knowledge
English fluency
Travel readiness

Ausbildung

MSc/BSc in mechanical or mechatronics

Tools

SolidWorks
ERP system

Jobbeschreibung

Distalmotion SA seeks a Robotics Manufacturing Engineer to drive industrialization and manufacturing engineering for the Dexter surgical robot and its accessories. You will own sustaining engineering, manufacturing testing, RCAs, and design transfer in a regulated ISO 13485 environment at the CMO site.

You will collaborate across functions to support ramp-up, perform root-cause analysis, and lead change-control activities while ensuring documentation and QMS compliance.

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