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Johnson & Johnson

Makes prescription drugs and medical devices

Operations Process Engineer - Capital System

Quality EngineeringConfirmed live in the last 24 hours
Full-timeSanta Clara, CA, USA$75k - $120.8k

About the Job

Requirements

  • A bachelor's degree in Engineering or a related technical discipline.
  • Zero to four years of relevant engineering experience; internship, co-op, academic project, research, or laboratory experience may be considered.
  • Hands-on experience with engineering testing, system integration, scripting, or technical troubleshooting through academic or professional work.
  • Ability to interpret test results and systematically troubleshoot hardware, software, and system-level failures.
  • Basic scripting experience, preferably with Python, and ability to read and debug scripts.
  • Strong analytical, problem-solving, technical writing, and communication skills.
  • Ability to work effectively with Manufacturing, Test Engineering, Quality, NPI Engineering, and R&D partners.
  • Ability to work 100% onsite.

Responsibilities

  • Ensure uninterrupted manufacturing operations and escalate issues when appropriate.
  • Support manufacturing activities associated with system integration and test.
  • Work directly with Manufacturing Associates and cross-functional engineering partners to identify and resolve technical issues affecting safety, quality, delivery, or production continuity.
  • Investigate manufacturing test failures using structured troubleshooting and problem-solving methods.
  • Troubleshoot test hardware, software, and system interfaces.
  • Document findings, define containment actions, and partner with Test, NPI Engineering, and Quality on permanent corrective actions.
  • Capture technical knowledge and recurring failure modes to improve troubleshooting consistency and reduce production downtime.
  • Support change controls, CAPAs, NCRs, and related quality system activities.
  • Participate in nonconformance investigations, root cause analysis, impact assessments, and implementation of corrective and preventive actions.
  • Ensure assigned manufacturing and documentation activities are performed in accordance with approved procedures and applicable quality requirements.

Desired Qualifications

  • Experience with Python, LabVIEW, MATLAB, automated test systems, data acquisition tools, SQL, or manufacturing data analysis.
  • Experience troubleshooting electromechanical systems, robotic systems, complex capital equipment, or integrated hardware/software products.
  • Exposure to a regulated manufacturing environment such as medical devices, pharmaceuticals, biotechnology, aerospace, or automotive.
  • Familiarity with change controls, CAPAs, NCRs, root cause analysis, and corrective action processes.
  • A hands-on, ownership-oriented approach and the ability to respond with urgency to production issues while maintaining quality and compliance.

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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