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Director, R&D and Product Development

Job in Brecksville, Cuyahoga County, Ohio, 44141, USA
Listing for: The Lubrizol Corporation
Full Time position
Listed on 2026-06-05
Job specializations:
  • Engineering
    Product Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below
Position: Director, R&D and New Product Development

Location: Brecksville, OH to start, and transitioning to Wickliffe, OH in 2028.

Job Type: Hybrid. 4 days on-site.

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.

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.

Responsibilities
  • 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
  • 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
  • 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
  • Competitive salary with performance‑based bonus plans
  • 401(k) match + Age‑Weighted Defined Contribution
  • Comprehensive medical, dental & vision coverage
  • Health Savings Account (HSA)
  • Paid holidays, vacation, and parental leave
  • Flexible work environment
  • Learning and development opportunities
  • Career and professional growth
  • Inclusive culture and vibrant community engagement
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