Senior Supervisor Supplier Engineering

Johnson & Johnson Johnson & Johnson · Pharma · Danvers, MA +1

This role leads a team of Supplier Engineers focused on managing supplier performance, product quality, and manufacturing scalability within the Electronics category. It involves being a technical interface with suppliers, driving qualification, process optimization, and lifecycle management, with a strong emphasis on "Quality at the Source" and process validation (IQ/OQ/PQ).

What you'd actually do

  1. Lead, coach, and develop a team of Supplier Engineers to deliver strong technical execution and business results
  2. Conduct performance management including goal setting (“What” and “How”), feedback, and development planning
  3. Foster an inclusive, high-performing team culture aligned with Leadership Imperatives
  4. Act as escalation point for complex technical and supplier issues
  5. Own strategic relationships with key suppliers for complex components, assemblies, and finished goods

Skills

Required

  • Bachelors degree in electrical engineering, manufacturing engineering or related fields
  • 5+ 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.
  • 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.
  • 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

Nice to have

  • masters degree preferred
  • Lean Six Sigma Green Belt or Black belt preferred
  • Experience designing and executing Gauge R&R studies preferred
  • Working knowledge of SAP a plus

What the JD emphasized

  • process validation plans, including IQ/OQ/PQ protocols/reports required
  • FDA 21CFR820/821 and ISO 13485 requirements