
Senior NPI Engineer
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
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Drive manufacturing process development from early design phases through commercial launch for complex electro‑mechanical medical devices.
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Develop, characterize, and optimize manufacturing processes for capital equipment, including assembly, test, calibration, and packaging operations.
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Support Design for Manufacturability (DFM) activities in collaboration with R&D, Quality, and Operations.
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Translate design requirements into manufacturing requirements, equipment specifications, and process documentation.
Process Validation & Manufacturing Readiness
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Own process validation activities (IQ/OQ/PQ) for in‑house equipment and supplier processes in compliance with ISO 13485 and Abbott procedures.
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Author validation plans, protocols, and summary reports.
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Create manufacturing documentation, including manufacturing requirements, equipment and process specifications, manufacturing procedures/work instructions/IPCs, test methods, and PFMEAs.
Manufacturing & Supplier Collaboration
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Serve as the technical interface between Abbott and external suppliers developing sub‑assemblies or performing outsourced manufacturing steps.
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Review supplier process flows, PFMEAs, control plans, and validation protocols.
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Align internal and external manufacturing processes for efficient production.
Required Qualifications
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Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Electrical Engineering, or a related technical discipline.
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5+ years of experience in medical device NPI, manufacturing engineering, or process development.
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Ownership in developing and validating manufacturing processes and tooling for electro‑mechanical or capital medical equipment.
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Strong working knowledge of process validation (IQ/OQ/PQ) and regulated manufacturing environments.
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Experience creating manufacturing requirements, specifications, and procedures, including developing/defining CTQs and IPCs
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Hands-on experience on the manufacturing floor to support engineering/pilot builds.
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Experience collaborating with and managing external suppliers for manufacturing processes or sub‑assemblies.
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Strong technical writing and communication skills; ability to collaborate with a cross-functional project team (R&D, Quality, Regulatory, etc.)
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English proficiency is required (English is used in meetings and all documentation)
Preferred Qualifications
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Experience with medical devices/equipment containing electronics, motors, LCD displays, and user interface components
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Proficiency using statistics, including gage R&R, DOE, capability studies (Cp/Cpk), and other analyses to ensure measurement and process robustness
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Experience with Lean Manufacturing and/or Six Sigma methodologies
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Experience supporting production ramp‑up and sustaining engineering after product launch
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Sustaining experience post-launch, e.g. yield improvement, root cause investigations, and ongoing process optimization
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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:
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Meaningful work that directly impacts patients’ lives
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Career growth opportunities within a global healthcare organization
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A stable and future-focused industry
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A collaborative and inclusive team culture
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A modern workplace in the heart of Zurich
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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/AIn 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