Experienced Supplier Engineer

Job Function Supply Chain Engineering Job Sub Function Process Engineering Job Category Scientific/Technology All Job Posting Locations Danvers, Massachusetts, United States of America Job Description We are searching for the best talent for Experienced Engineer, Supplier Process Engineering. The Experienced Supplier Engineer serves as ABIOMED’s primary technical contact with U.S. based suppliers, leads product development team’s supplier initiatives, second source critical suppliers, and establishes “Quality at the Source” programs with key partners. This role is a key technical resource for the company’s continued growth and is a great opportunity for someone to make a difference at one of the fastest-growing medical technology companies, focused on recovering hearts and saving lives. 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 them for continuous improvement activities leading to yield and quality improvements using 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 Bachelors or Masters degree in mechanical engineering, manufacturing engineering, plastics engineering or related disciplines 3+ years experience in 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, 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, vision system/optical comparator Ability to prioritize & complete tasks effectively to meet deadlines Working knowledge of Microsoft Office Suite, Analytical software’s like Minitab Willingness to travel up to 25% within the United States Benefits The anticipated base pay range for this position is: $79,000 - $127,000. This position is eligible for an annual performance bonus and long‑term incentive program. Employees may participate in the Company’s consolidated retirement plan (401(k)) and savings plan. Benefits include medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, and group legal insurance. Time‑off benefits: Vacation – up to 120 hours per calendar year; Sick time – up to 40 hours per calendar year (56 hours for employees residing in Washington State); Holiday pay, including floating holidays – up to 13 days per calendar year; Work, Personal and Family Time – up to 40 hours per calendar year. 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 under 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 applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us through the Company’s designated accommodation resource. #J-18808-Ljbffr Johnson & Johnson MedTech