Senior Product Development Engineer
Johnson & Johnson
full-time
Posted on:
Location Type: Office
Location: Danvers • Massachusetts • United States
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Salary
💰 $109,000 - $174,800 per year
Job Level
About the role
- 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 cross-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.
Requirements
- BS in Mechanical Engineering or directly related scientific field, MS Preferred
- 6 years of experience with Bachelor’s degree, or at least 5 years of experience 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 stakeholders, 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
- Product development experience in Class 3 Medical Device engineering MSc/MEng Preferred
- Applied understanding of DFM concepts and manufacturing best practices
- Working knowledge of SAP and Minitab desired
Benefits
- medical, dental, vision, life insurance
- short- and long-term disability
- business accident insurance
- group legal insurance
- consolidated retirement plan (pension)
- savings plan (401k)
- vacation – up to 120 hours per calendar year
- sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
- holiday pay, including Floating Holidays – up to 13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Medical Device Design ControlsProduct Life CycleDesign for Manufacturability (DFM)Test MethodsCADSolidworksFinite Element Analysis (FEA)3-D printingPrototypingEngineering documentation
Soft skills
CommunicationIndependent judgmentProblem-solvingLeadershipCollaborationPresentation skillsAttention to detailOrganizational skillsCritical thinkingInterpersonal skills
Certifications
BS in Mechanical EngineeringMS in Mechanical EngineeringMSc in related scientific fieldMEng in related scientific field