Product Development Engineer

Job Description Summary With direction from the GIE PPD Leader for UCC, the incumbent shall provide a leading Product & Process Design role in planning and execution of medical device projects for the Urology and Critical Care (UCC) Business Unit. They shall provide product design feedback and be the assembly subject matter expert (SME) for cross functional teams. The incumbent must be capable of specifying process technology, maintain timelines, associated project budgets and actively de‑risk all aspects for the product and process development. This role will require regular updates to the supporting management, cross‑function teams and BU Operational leadership. This position will require 25% travel that can be unevenly distributed throughout the year and can exceed 25% when business requirements are needed. Job Description We are the makers of possible. BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. Summary Of Position The mission of this role is the development of superior products and efficient processes through meticulous execution of design for manufacture & assembly (DFMA) enabling high impact innovation and sustainable growth. This role will assume technical leadership of projects and champion technical excellence in product assembly. This role will engage with R&D ensuring the manufacturability of new products. This candidate will have a passion for developing robust, well‑thought‑out medical device assembly equipment/processes that optimize for business success through production of high‑quality products with best‑in‑class OEE processes. This technical leader is a partner with R&D and Operations Assembly Equipment Design Team for new product introductions with a view to launching sophisticated manufacturing processes & automation while meeting the needs and timelines for customer focus. Responsibilities Define manufacturing technology strategy for new products, support product design by manufacturability analysis of the devices and their packaging and ensure a successful transfer to the production floor. Lead engineering efforts to build pilot lines of new manufacturing processes to attain process capability and OEE. Responsible for working with R&D across UCC on the design and development of current and new products. Perform DFA (Design For Assembly) and DFSS (Design For Six Sigma) analysis and establish assembly requirements and implement process controls to ensure product quality and consistency. Guide in design for manufacturability & assembly principles. Define manufacturing technology strategy for new products (NPD) and product design changes, influence product design through design for manufacture & assembly (DFMA) analysis and enable successful industrialization (internal or external) and transfer to the factories. Ensure the assembly process is understood well to minimize risk. Develop and implement assembly risk mitigation plans. Ensure execution of DFMA efforts will lead to achieving COGS/GP targets in business case. Support the development of DFMA standards and best practices for the Product Manufacturability and Assembly Design GIE team. Collect the opportunities for existing manufacturing processes and identify areas for improvement. Design new manufacturing processes that are efficient, within the targeted CapEx & COGS, and scalable. Suggest alternative design iterations, exploring various form factors, materials, functional solutions to address user needs and manufacturing constraints. Support process validations to ensure compliance with regulatory requirements. Collaborate multi‑functionally, especially with R&D and manufacturing specialists to ensure the design aligns with product requirements, and product designs are optimized for manufacturability, assembly, and overall performance. SME in DFMA, engineering, and process for assembly. Review and revise detailed CAD models of product designs, ensuring accuracy/alignment to specifications, standards and manufacturing requirements. Participate in design verification/testing activities. Present sophisticated data in a clear and concise manner to all levels of the organization. Align with all local, state, federal, and BD safety laws, policies, and procedures. Align with all local BD quality policies, procedures, and practices through consistent application of sound quality assurance principles. Support New Product Team Design Activities Including Provide technical leadership in the concept development of design control documentation. Works both independently and/or collectively to develop project plans and execution of prioritizing and scheduling assignments to meet business goals. Lead technical process reviews. Work with design team to ensure components/assemblies are designed for manufacturability/excellence (DFM/DFx). Able to plan, coordinate and lead all technical activities associated with commercialization and launch of new products including Conceptualization and development of all manufacturing processes and methods. Coordination of all development and manufacturing of new tooling and equipment. Support makes vs buy analysis and identifying new vendors. Support site selection activities. Coordination and support of all new vendor equipment, tooling, molds, etc. Support development of all products and process documentation. Support in‑process test and/or inspection procedure development. Planning, ordering and management of component inventory. Performing process characterization of all new operations and processes. Developing, implementing, analyzing, and writing reports for validation protocols. Developing new product cost estimates. Support preparation of capital equipment requisitions (CB2). Evaluation and recommendation of new materials. Qualifications Education BS degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or equivalent field and 10 years' experience OR MBA or MS in Engineering and 8 years' experience Experience 5 years of experience in advanced manufacturing engineering, product design, and/or technical leadership level in Medical Device or other highly regulated industries OR 5 years of professional experience in mechanical design, with a significant and demonstrable focus on applying DFMA principles. DFSS, DFMA, Tolerance Stack-Up Analysis, CAD Modeling, Design Control, prior experience on a technical leadership role, Risk analysis / FMEA is a must‑have. Medical device experience and Automation exposure are nice‑to‑have. Demonstrated experience leading/deploying Advanced Manufacturing initiatives. Digitalization and automation experience / exposure required. Sound capability to understand concepts and approaches in facilitating strong leadership expected. Experience in process validation, writing protocols and reports to support verification and validation activities for product commercialization; ability to complete validation. Experience with both manual and semi‑automated production lines preferred. Skills Intermediate/Advanced knowledge of design and simulation software such as SolidWorks, AutoCAD, ProModel, FlexSim. Able to act in multicultural environment and worldwide matrix organizations. Ability to build and implement project plans. Basic tooling, design and drafting knowledge. Ability to analyze data, interpret results, and write reports. Proficient in statistical software. Excellent technical skills including project management, organization, planning, and capital budgets. Excellent Interpersonal Skills - able to express ideas and collaborate optimally with multidisciplinary teams. Ability to work with minimal guidance, conceptualize ideas, motivate, and focus individuals and teams and drive projects through completion on time and on budget. Understanding and ability to implement DOEs, process characterizations and validations using standard statistical techniques. Understanding of GMPs and medical device regulations as they apply to manufacturing. Ability to interpret, edit and correct part drawings. Understanding of GD&T. Risk analysis / FMEA. Understanding of project management and budgeting. Travel 25% of the time Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit Equal Opportunity Statement Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics. Workplace and Accommodations At BD, we prioritize on‑site collaboration because we believe it fosters creativity, innovation, and effective problem‑solving, which are essential in the fast‑paced healthcare industry. For most roles, we require a minimum of 4 days of in‑office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work‑life balance. Remote or field‑based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID‑19. In some locations, testing for COVID‑19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Locations Primary Work Location: USA GA - Covington BMD Additional Locations: TBD Work Shift: TBD #J-18808-Ljbffr BD