Senior NPI & Manufacturing Engineer – Medical Devices

Abbott AG

Zürich

On-site

CHF 120,000 - 180,000

Full time

4 days ago
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Benefits offered by this job

Global cross‑functional team
Opportunities for growth
Impact on patient lives

Job summary

Abbott AG in Zürich is seeking a Senior Operations & NPI Engineer to lead industrialization and validation of complex electromechanical medical devices. You will work across R&D, Quality, Regulatory, Operations, and suppliers to transition from development to large-scale manufacturing.

The role emphasizes design-for-manufacture input, robust test systems, and data-driven process improvements, with a global collaboration between Zurich and Pleasanton.

Qualifications

  • Degree in a relevant engineering field is required.
  • Experience driving new product introductions and manufacturing scale-up.
  • Experience with cross-functional development teams and data analysis.

Responsibilities

  • Lead transfer of new products from R&D to manufacturing for scalable production.
  • Develop processes, production workflows, and manufacturing docs for new products.
  • Provide DfM/DFx feedback to R&D across product lifecycle.
  • Design and qualify production test systems, fixtures, and tools.
  • Define routings, BOMs, and master data in SAP.
  • Coordinate industrialization with R&D, QA, supply chain, and suppliers.
  • Define validation strategies including IQ/OQ/PQ activities.
  • Analyze manufacturing data to monitor process capability and quality.
  • Identify risks and drive corrective actions for launches.
  • Support pilot builds, engineering builds, and ramp-up,

Skills

NPI experience
Cross-functional teamwork
Process validation
Manufacturing engineering
ERP / SAP
Statistical analysis
English language

Education

Bachelor's/Master's in Mechanical/Electrical/Manufacturing/Industrial/Mechatronics/Software

Tools

SAP

Job description

Abbott AG in Zürich is seeking a Senior Operations & NPI Engineer to lead industrialization and validation of complex electromechanical medical devices. You will work across R&D, Quality, Regulatory, Operations, and suppliers to transition from development to large-scale manufacturing.

The role emphasizes design-for-manufacture input, robust test systems, and data-driven process improvements, with a global collaboration between Zurich and Pleasanton.

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