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J&J Family of Companies

Sr Product Development Engineer

J&J Family of Companies, Danvers, Massachusetts, United States, 01923

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Sr. R&D Engineer

Johnson & Johnson is currently seeking a Sr. R&D Engineer to join our Heart Recovery engineering team located in Danvers, MA. This is an onsite position. Key Responsibilities: Build and innovate current medical, technical, and biomedical developments related to company products and heart recovery technologies. Lead product development improvement efforts per plan and with little to no direct supervision. Prepare, present and lead design reviews to attain agreement on project with peers and multi-functional review team. Develop and update design documentation including test protocols, reports, and engineering rationales to support both quality and regulatory documentation. Develop Test Methods and understand requirements for Validation. Support and/or drive sustaining activities of existing product lines, including involvement with Corrective and Preventive Actions. Fabricate prototypes with assistance from junior staff, technical support team (Machine Shop, Technicians and Designers) and suppliers. Maintain accurate documentation of concepts, designs, and processes. Resolve producibility issues with internal and external manufacturing partners. Work with internal and external manufacturing partners to ensure producible designs (DFM). Document designs by constructing solid models and drawings using GD&T and stack-up analyses. Perform evaluations, design and prototyping using CAD (Solidworks), FEA, 3-D printing to accelerate development and engineering of plastics, ceramic, composite and metallic parts, electromechanical systems, etc. Qualifications: Education: BS in Mechanical Engineering or directly related scientific field, MS or equivalent experience preferred. Experience and Skills: Required: 6 years of experience with Bachelor's degree, or demonstrated ability with a Master's degree. Thorough understanding of Medical Device Design Controls and Product Life cycle Knowledge of FDA and EU MDR regulations Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) with partners, project team, local and international. Ability to exercise independent judgment in methods, techniques and evaluation criteria for obtaining results. Ability to act independently to resolve methods and procedures. Must be proficient in Microsoft Office Suite. Preferred: Product development experience in Class 3 Medical Device engineering MSc/MEng Preferred Applied understanding of DFM concepts and manufacturing standard methodologies Working knowledge of SAP and Minitab desired. Other: On-Site (Danvers, MA) English required May require up to 10% travel

US & EU Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit

www.careers.jnj.com .