Experienced Supplier Engineer

At Johnson & Johnson (JNJ), we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . Job function: Supply Chain Engineering. Job sub function: Process Engineering. Job category: Scientific/Technology. Locations: Danvers, Massachusetts, United States of America. Job Summary We are searching for an Experienced Supplier Engineer, Supplier Process Engineering, to lead technical initiatives with manufacturers of custom injection molded or extrusion components. The role focuses on improving supplier performance, driving continuous improvement, and ensuring high quality standards. The candidate will work closely with design engineers, internal cross‑functional teams, and suppliers to support product development, process validation, and manufacturing excellence. Principal Duties and Responsibilities Act as the primary technical point of contact with suppliers who provide custom injection molded or extrusion components and/or multi‑component sub‑assemblies. Lead efforts at suppliers to drive continuous improvement activities leading to yield and quality improvements using a data‑driven approach and Lean Six Sigma methodologies. Drive suppliers to perform process constraints analysis and develop capacity increase plans based on Abiomed delivery forecasting using a risk‑based approach. Engage with design engineers at early stages of development projects to review specifications and drawings; suggest and evaluate different potential manufacturing methods. Utilize project management tools and skills to set milestone targets with suppliers and track and report out on deliverables. Collaborate with internal cross‑functional teams and suppliers to determine qualification deliverables including: Process Validations (IQ/OQ/PQ), Inspection Reports, Gage R&R, and Process Capability Analysis while offering appropriate support where needed. Act as a technical partner with internal incoming inspection teams to assess non‑conformances and collaborate with suppliers to perform root‑cause investigations. Support product development projects as a liaison responsible for supplier interactions and deliverables. Perform DFM activities by engaging suppliers early in development cycle to provide feedback for manufacturability improvements in the designs prior to production. Lead and manage supplier change notifications including but not limited to equipment, process or design changes. Collaborate with sourcing and development teams to determine criteria for supplier selection and supplier evaluation for new or second‑source projects. Provide mentorship and guidance to junior engineers on the team. Required Qualifications Bachelor's or Master's degree in mechanical engineering, manufacturing engineering, plastics engineering, or related disciplines. 3+ years of experience in a professional field; medical device experience preferred. Demonstrated experience designing, improving or supporting manufacturing of injection molded and/or extruded plastics components. Preferred knowledge of component assembly processes including gluing, press/snap fits, and chemical bonding. Experience with conducting equipment and process validations. Proven knowledge of Lean Manufacturing and Six Sigma methodologies. Excellent problem‑solving skills and a data‑driven approach to decision‑making. Basic metrology skills; experience with calipers, gauge pins, and vision system/optical comparator. Ability to prioritize & complete tasks effectively to meet deadlines. Working knowledge of Microsoft Office Suite and analytical software such as Minitab. Willingness to travel up to 25% within the United States. Preferred Skills and Knowledge Analytical reasoning. Computerized equipment skills. Emerging technologies, Gemba Kaizen, issue escalation, lean supply chain management. Problem solving, process control, process engineering, process oriented, product improvements. Science, technology, engineering, and math (STEM) application. Situational awareness, supply planning, technical research, technologically savvy, validation testing. Equal Opportunity Employment Johnson & Johnson is an 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, disability, protected veteran status, or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource. Compensation and Benefits The anticipated base pay range for this position is $79,000 – $127,000. The Company maintains highly competitive, performance‑based compensation programs and an annual performance bonus aligned with company goals. Employees may also be eligible to participate in the Company’s long‑term incentive program. Medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, group legal insurance. Eligibility for the Company’s consolidated retirement plan (pension and savings plan 401(k)). Vacation – up to 120 hours per calendar year. Sick time – up to 40 hours per calendar year (up to 56 hours in Washington). Holiday pay, including floating holidays – up to 13 days per calendar year. Work, personal and family time – up to 40 hours per calendar year. Additional information at . Application closing date: June 18, 2026. The posting may be extended at the Company’s discretion. #J-18808-Ljbffr 6942-ABIOMED Inc. Legal Entity