Supplier Engineer II

At Johnson & Johnson, 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 SubFunction:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Danvers, Massachusetts, United States of America

Johnson & Johnson is currently seeking a Supplier Engineer II to join our Supply Chain team located in Danvers, MA. This is a hybrid role.

At Johnson & Johnson, 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/ (/url. us. m. mimecastprotect. com/s/MR_SCqxD2Oivo14wsZygBQ?domain=jnj. com/) .

Principal Duties and Responsibilities:

• Act as the primary technical point of contact with suppliers who provide electronic components and custom assemblies (PCBAs, consoles, cables, batteries, housings, etc. ) as well as custom injection molded or extrusion components and/or multi-component sub-assemblies

• Lead frequently recurring meetings with suppliers to manage engineering projects, including process validations, failure analysis, component obsolescence mitigations and manufacturing capacity increases

• Partner with supplier's engineering teams to analyze manufacturing processes and use data to develop and execute yield improvement project plans

• Partner with supplier's engineering teams to perform process constraints analysis and develop capacity increase plans based on Abiomed delivery forecasting

• Assess risk through FMEAs and develop process validation plans (MVP, IQ/OQ/PQ) to be executed at supplier

• Partner with internal design teams to assess product lifecycle design changes and develop and execute qualification test plans

• Act as a technical partner with internal incoming inspection teams to assess defects and manage non-conformance investigations

• Use project management tools to set milestone targets with suppliers and track and report out on deliverables

• Support product development projects as a liaison responsible for supplier interactions and deliverables

• Influence development team by representing capabilities of the supplier and push for DFx (Design for Manufacturing and Test) improvements at the design phase

• Provide input on second source selection and qualify processes at second source suppliers

Required Qualifications:

• Bachelors degree required (masters degree preferred) in electrical engineering, manufacturing engineering or related fields

• 3+ years experience in professional field, preferably at a manufacturer who designs, manufactures and/or assembles electrical components, PCBAs or consoles/box builds, plastic/Injection molded parts

• Demonstrated experience in printed circuit board manufacturing, SMT process, electrical component and assembly design theory (including PCB, batteries, cables/connectors, displays, and console/box design and manufacturing)

• Demonstrated experience designing, improving or supporting manufacturing of injection molded and/or extruded plastics components

• Knowledge of the process flow for ordering, receiving and using custom direct materials; including generating incoming inspection plans, participating in MRB investigations, non-conformance generation and disposition, and management of product through ERP systems (SAP preferred)

• Demonstrated experience developing process validation plans, including IQ/OQ/PQ protocols/reports required. Experience designing and executing Gauge R&R studies preferred.

• Demonstrated experience with root cause investigation, including the ability to validate root cause by turning off and on the failure

• Knowledge of statistical process control, including run charts, IM-R charts, setting control limits and generally keeping a process in a state of control. Lean Six Sigma Green Belt or Black belt preferred.

• Basic metrology skills, including experience with calipers, gauge pins, vision system/optical comparator

• Working knowledge of project management fundamentals, including schedule and stakeholder management, conflict resolution and identifying critical path

• Working knowledge of Microsoft Office Suite

• Knowledge of FDA 21CFR820/821 and ISO 13485 requirements

• Working knowledge of SAP a plus

• Willingness to travel up to 20% within the United States

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 careers. jnj. com .

Pay Transparency:

The anticipated base pay range for this position is $91,800 to $124,200.

Additional Description for Pay Transparency:

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401k). This position is eligible to participate in the Company's long-term incentive program. Employees are eligible for the following time off benefits: Vacation - up to 120 hours per calendar year. Sick time - up to 40 h.