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Johnson & Johnson

Makes prescription drugs and medical devices

Manufacturing Lead

Product AssemblyConfirmed live in the last 24 hours
Full-timeSanta Clara, CA, USA

About the Job

Requirements

  • Minimum associate degree with 6–8 related years of experience, or an engineering, mechatronics, or equivalent degree with 6–8 years of related experience.
  • Experience as a Manufacturing Technician for a Type II or Type III medical device company or complex electromechanical capital equipment manufacturer, including hands-on experience with Good Documentation Practices.
  • Advanced mechanical and electrical troubleshooting skills, including multimeter use and isolation techniques.
  • Demonstrated experience leading teams, coordinating production activities, and driving execution in a manufacturing environment.
  • Experience mentoring, coaching, and developing manufacturing personnel.
  • Proficiency in SAP and MES/ERP systems.
  • Proficiency in multiple assembly and test tasks while meeting workmanship, safety, and productivity requirements.
  • Demonstrated experience with anti-static/electrostatic discharge principles and controls.
  • Ability to read mechanical and technical writing and understand detailed system and manufacturing procedures.
  • Familiarity with assembly tools including torque wrenches, screwdrivers, hand drivers, multimeters, isopropyl alcohol, various presses, and adhesives such as Loctite.
  • Ability to prioritize competing demands and support execution in a fast-paced manufacturing environment.

Responsibilities

  • Lead daily production floor activities to achieve safety, quality, delivery, and productivity targets.
  • Assign and coordinate technician work priorities based on production needs, staffing levels, and resource availability.
  • Mentor, coach, and develop manufacturing technicians; provide hands-on support for troubleshooting, assembly, and skill development.
  • Facilitate shift handoffs and communicate production status, priorities, risks, and critical issues to leadership and cross-functional teams.
  • Represent the production floor in daily performance meetings, operational reviews, and cross-functional discussions as directed by the supervisor.
  • Monitor production progress and escalate staffing, material, equipment, quality, and schedule issues that may affect business objectives.
  • Drive adherence to manufacturing procedures, quality standards, safety requirements, and training compliance.
  • Verify personnel are trained and qualified on applicable procedures, processes, and equipment before work execution.
  • Maintain proficiency across at least five subassemblies within the assigned subsystem and provide technical guidance while maintaining knowledge of overall system architecture.
  • Apply a high-level understanding of system-level integration and troubleshooting steps to help resolve complex issues.
  • Create, review, and release work orders in MES/ERP systems when required.
  • Troubleshoot complex electrical, mechanical, and software issues.
  • Assist engineering with root cause analysis and implement corrective actions.
  • Maintain accurate material transactions and cycle counts, and report shortages proactively.
  • Support quality improvement initiatives across manufacturing and cross-functional teams.
  • Ensure compliance with hazardous waste handling, calibration, and safety standards.
  • Lead Kaizen events and support Lean manufacturing projects.
  • Drive alignment between teams, shifts, departments, and cross-functional partners to improve operational effectiveness and collaboration.
  • Present on the shop floor and participate in departmental performance management meetings as required by the supervisor.
  • Determine and report shortages accurately; report quality or defective material and component issues as required.
  • Initiate, investigate, document, and close Incident Reports and Nonconformances as required, ensuring timely resolution and compliance with quality system requirements.

Desired Qualifications

  • Experience supporting New Product Introduction builds and change management implementation within a regulated manufacturing environment.
  • Participation in Lean manufacturing or Kaizen improvement events.
  • Six Sigma Yellow Belt certification or equivalent continuous improvement training.
  • Familiarity with structured problem-solving tools such as 5 Whys, Fishbone, and DMAIC-lite.
  • Experience training or certifying technicians across multiple system modules.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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