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Abbott is hiring a

Senior NPI Engineer

Zürich, Switzerland

JOB DESCRIPTION:

Senior NPI Engineer – New Product Introduction

Abbott is seeking a Senior New Product Introduction (NPI) Engineer to support the development and manufacturing scale up of the next generation CentriMag Circulatory Support System . This role will be a key contributor to transitioning complex, electromechanical medical devices from design through validated manufacturing—both in house and at external suppliers .

The ideal candidate brings hands on experience in process development , process validation , and manufacturing readiness for capital equipment containing electronics, displays, user interfaces (buttons, touchscreens, connectors), and electromagnetic motors , within a regulated medical device environment.

With your work, you’ll ensure these life-saving 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 Zurich and United States offices.

Main Responsibilities

New Product Introduction & Process Development

  • Drive manufacturing process development from early design phases through commercial launch for complex electro‑mechanical medical devices.

  • Develop, characterize, and optimize manufacturing processes for capital equipment, including assembly, test, calibration, and packaging operations.

  • Support Design for Manufacturability (DFM) activities in collaboration with R&D, Quality, and Operations.

  • Translate design requirements into manufacturing requirements, equipment specifications, and process documentation.

Process Validation & Manufacturing Readiness

  • Own process validation activities (IQ/OQ/PQ) for in‑house equipment and supplier processes in compliance with ISO 13485 and Abbott procedures.

  • Author validation plans, protocols, and summary reports.

  • Create manufacturing documentation, including manufacturing requirements, equipment and process specifications, manufacturing procedures/work instructions/IPCs, test methods, and PFMEAs.

Manufacturing & Supplier Collaboration

  • Serve as the technical interface between Abbott and external suppliers developing sub‑assemblies or performing outsourced manufacturing steps.

  • Review supplier process flows, PFMEAs, control plans, and validation protocols.

  • Align internal and external manufacturing processes for efficient production.

Required Qualifications

  • Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Electrical Engineering, or a related technical discipline.

  • 5+ years of experience in medical device NPI, manufacturing engineering, or process development.

  • Ownership in developing and validating manufacturing processes and tooling for electro‑mechanical or capital medical equipment.

  • Strong working knowledge of process validation (IQ/OQ/PQ) and regulated manufacturing environments.

  • Experience creating manufacturing requirements, specifications, and procedures, including developing/defining CTQs and IPCs

  • Hands-on experience on the manufacturing floor to support engineering/pilot builds.

  • Experience collaborating with and managing external suppliers for manufacturing processes or sub‑assemblies.

  • Strong technical writing and communication skills; ability to collaborate with a cross-functional project team (R&D, Quality, Regulatory, etc.)

  • English proficiency is required (English is used in meetings and all documentation)

Preferred Qualifications

  • Experience with medical devices/equipment containing electronics, motors, LCD displays, and user interface components

  • Proficiency using statistics, including gage R&R, DOE, capability studies (Cp/Cpk), and other analyses to ensure measurement and process robustness

  • Experience with Lean Manufacturing and/or Six Sigma methodologies

  • Experience supporting production ramp‑up and sustaining engineering after product launch

  • Sustaining experience post-launch, e.g. yield improvement, root cause investigations, and ongoing process optimization

  • Communicative German is a plus

Why Join Abbott / Thoratec?

At Abbott, we know that people do their best work when they feel supported, included, and empowered. We are committed to creating an environment where everyone can succeed.

You can expect:

  • Meaningful work that directly impacts patients’ lives

  • Career growth opportunities within a global healthcare organization

  • A stable and future-focused industry

  • A collaborative and inclusive team culture

  • A modern workplace in the heart of Zurich

  • An environment where different perspectives and experiences are valued

Ready to Apply?

We’re looking for curious, motivated people who want to grow and make a difference — not just those who meet every single requirement.

If this role sounds exciting to you, we’d love to hear from you.

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Manufacturing

DIVISION:

HF Heart Failure

LOCATION:

Switzerland : Technoparkstrass 1 CH 8005

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Not specified

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

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