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EMEA – Tyvek® Healthcare Innovation Technical Lead (m/f/d)
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Other
postgraduate degree
Comprehensive pay and benefits package
Posted 1d ago
~40 hrs/week
Responsibilities
The Technical Lead will identify and develop new application opportunities for Tyvek® healthcare products by translating market trends into technical solutions. They will lead cross-functional technical feasibility assessments and manage the transition of new applications from development to commercialization.
Requirements
Candidates must hold a Master or PhD in a relevant technical discipline such as Packaging Engineering or Materials Science. A minimum of 5 years of experience in R&D or technical innovation within the Life Sciences sector is required.
Full job description
At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it’s providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world’s most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers
DuPont Healthcare & Water is globally recognized for advanced materials and solutions. With Tyvek®, DuPont improves safety & health, innovation, and sustainability in healthcare packaging, personal protective equipment, and consumer & industrial solutions.
DuPont is seeking a Tyvek® Healthcare – Innovation Technical Lead for its Tyvek® Roll Goods Business. Operating in a 2‑in‑a‑box model with the Global Tyvek® Healthcare Innovation Market Lead, this role will identify, prioritize, and develop new applications and platforms.
What You'll Do
New Application and Opportunity Identification
Identify new application opportunities based on market trends and customer needs.
Translate customer and market insights into technical opportunity concepts and application hypotheses.
Technical Strategy and Feasibility
Define technical value proposition, performance targets, and differentiation.
Lead technical feasibility assessments, including evaluation of performance, scalability, manufacturability, cost structure, and sustainability considerations.
Identify technical risks, gaps, and development needs, and propose mitigation strategies.
Application Development and Validation
Lead early-stage application development activities.
Develop and execute testing and validation plans.
Incorporate customer, market, and technical feedback to refine solutions through iterative development cycles.
Cross-Functional and External Collaboration
Serve as the primary technical interface for new business initiatives, collaborating closely with Tyvek® Healthcare cross-functional teams.
Establish and leverage external technical collaborations.
Portfolio Prioritization and Business Support
Support business case development by contributing technical assumptions.
Enable informed decision-making through fact-based technical assessments.
Provide technical input into opportunity prioritization, portfolio reviews, and stage-gate or governance processes.
Transition to Commercialization
Define technical roadmaps to support transition from early development to commercialization readiness.
Support effective handover of mature opportunities to Product Management, Business Units, or Technology organizations.
What You'll Bring
Required
Master or PhD in Packaging Engineering, Materials Science, Pharmaceutical Sciences, Mechanical Engineering or related technical discipline.
Minimum 5 years of experience in R&D, application development, or technical innovation roles in Life Sciences.
Demonstrated ability to translate customer and market needs into technical solutions.
Proven experience leading cross-functional technical projects in complex or ambiguous environments.
Strong analytical, problem-solving, and communication skills.
Ability to work effectively in an agile, exploratory, and fast-paced environment.
Travel up to 30%.
Preferred
Strong experience in pharmaceutical or biopharmaceutical manufacturing, particularly in lyophilization processes.
Strong understanding of Good Manufacturing Practices (e.g. GMP Annex 1 and contamination control principles and practices), ISO 15378, ISO 11607, and ICH guidelines.
Familiarity with innovation funnels, stage-gate processes.
DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit ourAccessibility Page for Contact Information.
Beware of recruitment scams! Please read important information for job seekers: https://www.dupont.com/careers/hiring-faqs.html
We’re creating advanced solutions that help transform industries and improve everyday life across our key markets of healthcare, water, construction and transformation. At DuPont, we inspire each employee to embrace their unique journey and unlock their full potential. Discover the many reasons to work at DuPont.
Learn more at dupont.com.
Please take the time to review our comments policy before commenting on our page. http://dptn.ws/policy
Offices: 974 Centre Road,, Wilmington, DE 19805, US
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