Service Project Engineer – MedTech & Capital Equipment

Johnson & Johnson MedTech

Amersfoort

Vor Ort

EUR 45.000 - 71.000

Vollzeit

vor 34 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Annual bonus
Vacation days
Well-being reimbursement
Parental leave

Zusammenfassung

Johnson & Johnson MedTech, based in Amersfoort, Netherlands, is seeking a Service Project Engineer to join the EMEA Service Centers. The role focuses on developing, validating, and improving service and repair processes for capital medical devices, with hands-on technical support and cross-functional collaboration.

Responsibilities include leading engineering projects, validating IQ/OQ/PQ activities, and ensuring safety, quality, cost, and delivery requirements are met across new products and

Qualifikationen

  • Bachelor's degree in Manufacturing/Mechanical/Industrial Engineering or comparable field.
  • Minimum 4 years in manufacturing/process/project engineering or capital equipment service.
  • Experience with process development, troubleshooting, validation, and documentation.

Aufgaben

  • Design, develop, and improve service and repair processes for capital medical devices.
  • Lead engineering projects of low to medium complexity and coordinate with cross-functional teams.
  • Plan and execute Computer System Validation and equipment/process validation activities (IQ/OQ/PQ).
  • Provide day-to-day engineering support across the service portfolio, including various capital equipment platforms.
  • Manage project scope, schedules, risks, and costs; communicate progress to stakeholders.

Kenntnisse

Communication
English proficiency
Dutch proficiency
Office software

Ausbildung

Bachelor's degree in Manufacturing/Mechanical/Industrial Engineering

Tools

Microsoft Office
Validation tools (IQ/OQ/PQ)

Jobbeschreibung

Johnson & Johnson MedTech, based in Amersfoort, Netherlands, is seeking a Service Project Engineer to join the EMEA Service Centers. The role focuses on developing, validating, and improving service and repair processes for capital medical devices, with hands-on technical support and cross-functional collaboration.

Responsibilities include leading engineering projects, validating IQ/OQ/PQ activities, and ensuring safety, quality, cost, and delivery requirements are met across new products and

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