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Johnson & Johnson
Johnson & Johnson
Sponsor pentru viza H1BAsigurare de sănătateAsistență medicalăProduse farmaceutice
Johnson & Johnson este o companie globală din domeniul sănătății, care activează în medicina inovatoare și tehnologia medicală. Echipele sale dezvoltă soluții în oncologie, imunologie, neuroștiință, oftalmologie de specialitate, îngrijire intervențională și ortopedie, combinând știința și tehnologia pentru a răspunde unor nevoi complexe de sănătate. Compania pune, de asemenea, accent pe echitatea în sănătate, sustenabilitatea mediului, diversitate și incluziune, deservind furnizori de servicii medicale, pacienți și comunități din întreaga lume.
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Equipment Engineer - OTTAVA Robotic Surgery Platform, Santa Clara Onsite

Manage, qualify, troubleshoot, and improve manufacturing and test equipment supporting Johnson & Johnson’s OTTAVA robotic surgery platform. The role focuses on regulated production assets, equipment performance, reliability, and compliance.

USStatele Unite ale AmericiiCACaliforniaLa sediuNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăInginer

Descriere

  • Manage assigned manufacturing and test equipment from specification and selection through design review, FAT/SAT, installation, commissioning, qualification, release, maintenance, modification, and retirement.
  • Prepare or support URS/FRS documents, risk assessments, engineering drawings, maintenance strategies, spare-parts plans, calibration requirements, work instructions, change records, and validation protocols and reports.
  • Diagnose electrical, mechanical, pneumatic, robotic, controls, software-interface, and computer-related equipment failures while protecting personnel, product quality, data integrity, and the validated state.
  • Track equipment availability and uptime, evaluate downtime events, MTBF, MTTR, work-order history, repeat failures, and response effectiveness, and implement corrective and preventive actions.
  • Investigate performance losses such as slow cycles, micro-stops, jams, intermittent faults, and reduced operating rates.
  • Evaluate quality losses involving equipment-related defects, rework, false failures, measurement-system problems, and calibration drift.
  • Apply structured problem-solving methods, including 5 Whys, fault-tree analysis, fishbone diagrams, FMEA, and data trending, to prevent recurring failures and confirm corrective-action effectiveness.
  • Maintain accurate CMMS work orders and asset records, using maintenance history to optimize preventive-maintenance tasks, frequencies, spare parts, and equipment readiness.
  • Coordinate suppliers and technicians, support audits and inspections, and train users in safe, compliant equipment operation.

Cerințe

  • Bachelor’s degree in Mechanical, Electrical, Mechatronics, Manufacturing, Controls, Biomedical Engineering, or a related technical field; equivalent relevant experience may be accepted under company requirements.
  • At least 2 years of relevant experience in equipment, automation, maintenance, manufacturing, or test engineering within medical devices, robotics, life sciences, semiconductors, aerospace, or another regulated industry.
  • Hands-on experience with electromechanical equipment, automated test systems, robotics, controls, instrumentation, pneumatics, sensors, calibration, or custom fixtures.
  • Practical knowledge of GMP, design controls, controlled documentation, change control, deviation and nonconformance processes, and equipment qualification principles.
  • Experience analyzing equipment data, downtime records, yield or first-pass results, and maintenance history to identify OEE losses and improvement opportunities.
  • Understanding of OEE Availability, Performance, and Quality components, including the operational data required to calculate and interpret them.
  • Systematic troubleshooting skills and the ability to make safe decisions under production pressure.
  • Ability to interpret schematics, wiring diagrams, CAD drawings, technical specifications, PLC and controls information, and validation protocols.
  • Proficiency with CMMS platforms, technical writing, controlled documentation, and change-control execution.
  • Effective cross-functional communication with Manufacturing, Quality, R&D, Validation, EHS, Facilities, IT/OT, technicians, and suppliers.

Beneficii

  • Inclusive workplace environment.
  • Equal employment opportunity.
  • Interview accommodations are available for applicants with disabilities.

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