Director, R&D and New Product Development

Director, R&D and New Product Development Date: Aug 1, 2026 Location: Conrona, CA;Brecksville, OHwith a planned transitioning to Wickliffe, OH in 2028. As Lubrizol approaches its centennial in 2028, our Wickliffe campus will become the unified home of Lubrizol’s global headquarters , integrating Lubrizol’s Brecksville site capabilities and employees to the Wickliffe campus. Job Type: Hybrid. 4 days on-site Salary Range: $160,000.00-$220,000.00 + Bonus Travel Expectancy: 20 -40% Shape the Future with Us. At Lubrizol, we’re bringing to life the chemistry behind clean water, efficient transportation, reliable infrastructure, critical medicines, and the products people rely on every day through science, sustainability, and a culture of inclusion. As part of our global team, you’ll be empowered to make a real impact - on your career, your community, and the world around you. How You’ll Make an Impact The Global Leader, New Product Development – Medical Devices is a senior technical and people leader responsible for medical device new product development, from concept through commercialization. This role owns NPD strategy, talent development, governance, and execution across multiple geographies and development centers, ensuring strong alignment with customer needs, regulatory requirements, and business strategy. The role leads a global, multidisciplinary NPD organization, partners closely with Quality, Regulatory, Manufacturing, Commercial, and Executive Leadership, and acts as a senior technical representative to key medical device OEM customers. Required Qualifications that Enable Your Success Define and execute the global medical device NPD strategy aligned with business growth priorities, customer roadmaps, and portfolio strategy. Identify and pursue adjacent medical device applications where our technologies and platforms can create differentiated value and drive organic growth. Lead capability road mapping to define and build the new technical, testing, and development capabilities the group must invest in to sustain growth and capture high value programs. Establish scalable development governance, stage-gate rigor, and portfolio prioritization to ensure consistent execution excellence. Oversee complex, multi-site development programs from concept through commercialization, ensuring delivery to cost, schedule, performance, and quality expectations. Partner with Quality and Regulatory to ensure compliance with FDA, CE/MDR, ISO 13485, and applicable global regulatory requirements. Serve as senior technical interface with strategic OEM customers, supporting complex development engagements and long-term partnerships. Collaborate with Commercial, Marketing, and Business Development to shape development proposals, technology roadmaps, and differentiated customer solutions. Champion design-for-manufacturability, design-for-quality, and design-for-cost principles across global manufacturing platforms. Ensure effective transfer of products from NPD to Manufacturing, preserving design intent, robustness, and scalability during launch and ramp-up. Lead and develop a global organization of NPD engineers, scientists, and program leaders across multiple regions and sites. Build technical bench strength through hiring, development, coaching, and succession planning. Required Qualifications that Enable Your Success Bachelor’s degree in Mechanical, Biomedical, Chemical Engineering, or related technical discipline; advanced degree preferred. 10 or more years of progressive experience in medical device product development in a regulated environment., including experience in thermoplastic precision extrusion and silicone processing. Demonstrated experience leading global or multi-site technical teams. Strong working knowledge of FDA design controls, ISO 13485, FDA 21 CFR Part 820, and CE/MDR requirements. Proven track record delivering complex development programs from concept through commercialization and manufacturing transfer. Preferred Qualifications that Drive you Forward Advanced technical degree (MS or PhD). Experience with catheter-based or minimally invasive medical device technologies. Strong understanding of polymer-based medical devices and associated manufacturing processes. Formal training or certification in program or portfolio management. Experience operating effectively within matrixed global organizations. Benefits that Empower You Competitive salary with performance-based bonus plans 401(k) match + Age-Weighted Defined Contribution Health Savings Account (HSA) Paid holidays, vacation, and parental leave Lubrizol: Imagined for Life. Enabled by Science. ™ Delivered by You. For nearly 100 years, The Lubrizol Corporation, a Berkshire Hathaway company, has been at the forefront of innovation to enhance everyday life, advance mobility, and make the modern world work better. Our specialty chemistry solutions—from engine oils, performance coatings, and skincare to medical devices and plumbing systems —are powered by the expertise, passion, and commitment of people like you. We tackle the world’s toughest challenges with science-based solutions, deeply understanding our customers to deliver innovative chemistry and differentiated value. Our inclusive culture, dedication to safety, and incredible global talent drive our success. Our solutions meet the evolving needs of the modern world—brought to life by science and, most importantly, delivered by you. Whether you're in the lab, on the production floor, or in the office, you'll be part of a team around the world that empowers you to think boldly, drive results, and contribute to solutions that shape a better, more sustainable future. We win because of you. Let’s build the future together.

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Nearest Major Market: Corona Nearest Secondary Market: Los Angeles Job Segment: Chemical Research, R&D Engineer, Product Development, R&D, Compliance, Engineering, Research, Legal #J-18808-Ljbffr Lubrizol Corporation