<div><div><div><div><div><div><div><div><div><div><p><b>Senior NPI Engineer – New Product Introduction</b></p><p></p><p><span><b>Abbott</b> is seeking a <b>Senior New Product Introduction (NPI) Engineer</b> to support the development and manufacturing scale</span><span>‑</span><span>up of the <b>next</b></span><b><span>‑</span></b><b><span>generation CentriMag Circulatory Support System</span></b><span>. This role will be a key contributor to transitioning complex, electromechanical medical devices from design through validated manufacturing—both <b>in</b></span><b><span>‑</span></b><b><span>house</span></b><span> and at <b>external suppliers</b>.</span></p><p></p><p><span>The ideal candidate brings hands</span><span>‑</span><span>on experience in <b>process development</b>, <b>process validation</b>, and <b>manufacturing readiness</b> for capital equipment containing <b>electronics, displays, user interfaces (buttons, touchscreens, connectors), and electromagnetic motors</b>, within a regulated medical device environment.</span></p><p></p><p>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.</p><p></p><p><b>Main Responsibilities</b></p><p></p><p><b>New Product Introduction & Process Development</b></p><ul><li><p>Drive manufacturing process development from early design phases through commercial launch for complex electro‑mechanical medical devices.</p></li><li><p>Develop, characterize, and optimize manufacturing processes for capital equipment, including assembly, test, calibration, and packaging operations.</p></li><li><p>Support <b>Design for Manufacturability (DFM)</b> activities in collaboration with R&D, Quality, and Operations.</p></li><li><p>Translate design requirements into manufacturing requirements, equipment specifications, and process documentation.</p></li></ul><p></p><p><b>Process Validation & Manufacturing Readiness</b></p><ul><li><p>Own <b>process validation activities (IQ/OQ/PQ)</b> for in‑house equipment and supplier processes in compliance with ISO 13485 and Abbott procedures.</p></li><li><p>Author validation plans, protocols, and summary reports.</p></li><li><p>Create manufacturing documentation, including manufacturing requirements, equipment and process specifications, manufacturing procedures/work instructions/IPCs, test methods, and PFMEAs.</p></li></ul><p></p><p><b>Manufacturing & Supplier Collaboration</b></p><ul><li><p>Serve as the technical interface between Abbott and external suppliers developing sub‑assemblies or performing outsourced manufacturing steps.</p></li><li><p>Review supplier process flows, PFMEAs, control plans, and validation protocols.</p></li><li><p>Align internal and external manufacturing processes for efficient production.</p></li></ul><p></p><p><b>Required Qualifications</b></p><ul><li><p>Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Electrical Engineering, or a related technical discipline.</p></li><li><p>5+ years of experience in medical device NPI, manufacturing engineering, or process development.</p></li><li><p>Ownership in developing and validating manufacturing processes and tooling for electro‑mechanical or capital medical equipment.</p></li><li><p>Strong working knowledge of process validation (IQ/OQ/PQ) and regulated manufacturing environments.</p></li><li><p>Experience creating manufacturing requirements, specifications, and procedures, including developing/defining CTQs and IPCs</p></li><li><p>Hands-on experience on the manufacturing floor to support engineering/pilot builds.</p></li><li><p>Experience collaborating with and managing external suppliers for manufacturing processes or sub‑assemblies.</p></li><li><p>Strong technical writing and communication skills; ability to collaborate with a cross-functional project team (R&D, Quality, Regulatory, etc.)</p></li><li><p>English proficiency is required (English is used in meetings and all documentation)</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>Experience with medical devices/equipment containing electronics, motors, LCD displays, and user interface components</p></li><li><p>Proficiency using statistics, including gage R&R, DOE, capability studies (Cp/Cpk), and other analyses to ensure measurement and process robustness</p></li><li><p>Experience with Lean Manufacturing and/or Six Sigma methodologies</p></li><li><p>Experience supporting production ramp‑up and sustaining engineering after product launch</p></li><li><p>Sustaining experience post-launch, e.g. yield improvement, root cause investigations, and ongoing process optimization</p></li><li><p>Communicative German is a plus</p></li></ul><p></p><p><b>Why Join Abbott / Thoratec?</b></p><p></p><p>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.</p><p></p><p>You can expect:</p><ul><li><p><b>Meaningful work</b> that directly impacts patients’ lives</p></li><li><p><b>Career growth opportunities</b> within a global healthcare organization</p></li><li><p>A <b>stable and future-focused industry</b></p></li><li><p>A <b>collaborative and inclusive team culture</b></p></li><li><p>A modern workplace in the heart of Zurich</p></li><li><p>An environment where <b>different perspectives and experiences are valued</b></p></li></ul><p></p><p><b>Ready to Apply?</b></p><p></p><p>We’re looking for curious, motivated people who want to grow and make a difference — not just those who meet every single requirement.</p><p>If this role sounds exciting to you, we’d love to hear from you.</p><p></p><p></p></div></div></div></div></div></div></div></div></div></div>
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