Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Leads the design and development of complex medical devices from concept through to design freeze</li><li>Solves high-level engineering challenges using advanced materials knowledge, precision manufacturing methods, and data-driven decision making</li><li>Acts as a subject matter expert in catheter systems, extrusion-based assemblies, and biomaterials, influencing design direction and technical standards</li><li>Develops and executes verification and validation protocols (IQ/OQ/PQ), ensuring compliance with ISO 13485 and FDA 21 CFR Part 820</li><li>Manages cross-functional technical projects, balancing design intent, manufacturability, and regulatory requirements</li><li>Leads FMEA, risk analysis, and root cause investigations to ensure robust design and process outcomes</li><li>Provides technical mentoring and reviews for junior engineers and project teams, helping to build capability and ensure knowledge transfer</li><li>Drives innovation by exploring emerging technologies, novel components, and automation opportunities</li><li>Develops and maintains detailed documentation including DHFs, BOMs, drawings, and test reports in compliance with QMS requirements</li><li>Engages directly with customers to understand application needs, presenting technical solutions and leading design iterations</li></ul><h1>Qualifications:</h1><ul><li>Third-level qualification in Engineering or Science, preferably Mechanical or Biomedical; minimum Bachelor’s degree in Science, Technology, Engineering, or a related discipline (Mechanical, Manufacturing, Automation, or equivalent).</li><li>Proven design capability with CAD systems, ideally Solid Edge.</li><li>Senior-level candidates should have a minimum of 4 years’ relevant experience.</li><li>Excellent interpersonal and communication skills, with the ability to collaborate effectively across teams</li></ul>The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.VistaMed Ltd.

Freudenberg e-Power Systems is one of the world's leading suppliers of emission-neutral energy systems for heavy-duty applications. With its experience and expertise in battery and fuel cell technology, the company offers tailor-made solutions, in particular combined systems, for sustainable and economical e-mobility. With over 800 employees, Freudenberg e-Power Systems supports its customers from application development through to production, commissioning and service.
The company is part of the global Freudenberg Group, which has four business areas: Seals and Vibration Control Technology, Nonwovens and Filtration, Household Products as well as Specialties and Others. In 2022 the Group generated sales of more than 11 billion euros and employed more than 50,000 associates in around 60 countries.

Senior Research & Development Engineer

Working at Freudenberg: We will wow your world!<h1>Responsibilities:</h1><ul><li>Leads the design and development of complex medical devices from concept through to design freeze</li><li>Solves high-level engineering challenges using advanced materials knowledge, precision manufacturing methods, and data-driven decision making</li><li>Acts as a subject matter expert in catheter systems, extrusion-based assemblies, and biomaterials, influencing design direction and technical standards</li><li>Develops and executes verification and validation protocols (IQ/OQ/PQ), ensuring compliance with ISO 13485 and FDA 21 CFR Part 820</li><li>Manages cross-functional technical projects, balancing design intent, manufacturability, and regulatory requirements</li><li>Leads FMEA, risk analysis, and root cause investigations to ensure robust design and process outcomes</li><li>Provides technical mentoring and reviews for junior engineers and project teams, helping to build capability and ensure knowledge transfer</li><li>Drives innovation by exploring emerging technologies, novel components, and automation opportunities</li><li>Develops and maintains detailed documentation including DHFs, BOMs, drawings, and test reports in compliance with QMS requirements</li><li>Engages directly with customers to understand application needs, presenting technical solutions and leading design iterations</li></ul><h1>Qualifications:</h1><ul><li>Third-level qualification in Engineering or Science, preferably Mechanical or Biomedical; minimum Bachelor’s degree in Science, Technology, Engineering, or a related discipline (Mechanical, Manufacturing, Automation, or equivalent).</li><li>Proven design capability with CAD systems, ideally Solid Edge.</li><li>Senior-level candidates should have a minimum of 4 years’ relevant experience.</li><li>Excellent interpersonal and communication skills, with the ability to collaborate effectively across teams</li></ul>The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.VistaMed Ltd.

Senior Research & Development Engineer

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About the Company

Freudenberg

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