Global Product Development Leader - Injection Molded Components
DuPont™ Spectrum™ · Minneapolis, MN · 4 wk ago
MarketingFull-time
Key Responsibilities
- Develop and execute the global technology roadmap for injection molded healthcare components.
- Identify emerging manufacturing technologies, materials, automation solutions, and industry trends to support future business growth.
- Establish technical standards, best practices, and governance processes across the global manufacturing network.
- Drive technology differentiation and innovation to strengthen the company’s competitive position.
- Provide technical leadership for customer development programs and commercialization projects.
- Ensure successful transfer of new products from development into manufacturing.
- Support Design for Manufacturability (DFM), Design for Quality (DFQ), Design for Cost (DFC), Design for Assembly (DFA), and risk management activities.
- Collaborate with Application Development and Product Management teams to accelerate customer solutions and growth opportunities.
- Lead resolution of complex technical challenges affecting quality, delivery, or customer satisfaction.
- Utilize structured problem-solving methodologies to drive root cause analysis and corrective actions.
- Support continuous improvement initiatives across manufacturing sites.
- Develop technical knowledge-sharing and best-practice deployment processes.
Qualifications
- Bachelor’s degree in Engineering, Polymer Science, Materials Science, Mechanical Engineering, or related discipline required.
- Advanced degree Highly preferred.
- 15+ years of experience in injection molding, manufacturing technology, process engineering, or related technical leadership roles.
- 10+ years’ experience with advanced degree may be considered.
- Demonstrated experience leading global technical teams in a healthcare, medical device, life sciences, or highly regulated manufacturing environment.
- Deep expertise in injection molding processes, tooling, materials, validation, and manufacturing scale-up.
- Experience with medical-grade polymers, cleanroom manufacturing, automation, and quality systems preferred.
- Strong knowledge of FDA, ISO 13485, GMP, and other regulated manufacturing requirements preferably in polymer CDMO space.
- Proven ability to influence senior leaders and drive cross-functional alignment.