Johnson & Johnson

Manager, Tool and Test Equipment - Service

Johnson & Johnson$118K — $203K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience managing test equipment and calibration in regulated medical device settings
  • Strong project management skills with multi-phase initiative execution
  • Experience in supporting regulatory inspections and audits
  • Solid understanding of metrology concepts and equipment traceability
  • Proficiency in electronic calibration management tools (e.g., SimplerQMS)
  • Advanced data analysis skills using Power BI
  • Excellent communication and collaboration skills across departments

Responsibilities

  • Lead the lifecycle management of tools and test equipment in compliance with ISO and regulatory standards
  • Develop supplier evaluation and qualification programs adhering to FDA guidelines
  • Create risk-based calibration schedules and ensure proper documentation upkeep
  • Conduct investigations on out-of-tolerance equipment to maintain product quality
  • Forecast equipment obsolescence and develop retirement strategies
  • Analyze data to drive continuous improvement in service performance metrics
  • Prepare and maintain SOPs and audit readiness for equipment management

Benefits

  • Medical, dental, and vision insurance
  • Short- and long-term disability coverage
  • 401(k) retirement plan participation
  • Generous vacation and sick leave policies
  • Parental leave for new parents
  • Volunteer leave to support community service activities
  • Comprehensive legal insurance options
Full Job Description
Job Function: Supply Chain Manufacturing

Job Sub Function:

Robotics Service & Repair

Job Category:

Professional

All Job Posting Locations:

Santa Clara, California, United States of America

Job Description:

Johnson & Johnson MedTech is currently recruiting for a Manager, Tool and Test Equipment. This role is based in Santa Clara, CA.

Position Summary

The Manager, Tool & Test Equipment is a strategic and operational leader responsible for the full lifecycle management of all tools and test equipment within a medical device service environment. This role ensures all equipment is selected, procured, calibrated, maintained, analyzed, and decommissioned in compliance with ISO 13485, ISO 9001, MDSAP, EU MDR, and FDA 21 CFR Part 820 requirements.

This position sits at the intersection of engineering, quality, supply chain, and compliance—supporting field service and manufacturing teams to deliver safe, accurate, efficient, and fully compliant medical device services.

Key Responsibilities

Tool & Equipment Lifecycle Management

  • Lead risk-based selection and justification of measurement and test equipment.

  • Review technical documentation and regulatory requirements to determine measurement precision, tolerances, and traceability.

  • Maintain a master equipment register and oversee SOPs related to tool selection and qualification.

Supplier & Calibration House Management

  • Develop and manage supplier evaluation and qualification programs in accordance with ISO and FDA purchasing controls.

  • Audit and manage relationships with OEMs, calibration houses, and distributors.

  • Oversee contract negotiations, service-level agreements, performance scorecards, and corrective action management.

Calibration Program Oversight

  • Develop a risk-based calibration schedule aligned with regulatory and OEM requirements.

  • Utilize digital calibration management or CMMS systems for automated tracking and recordkeeping.

  • Ensure adherence to labeling, scheduling, and documentation requirements.

Out-of-Tolerance (OOT) Investigations

  • Quarantine and assess the impact of OOT equipment on product or service performance.

  • Lead root-cause investigations and coordinate CAPA actions.

  • Ensure thorough regulatory documentation and audit readiness.

Obsolescence Planning & Decommissioning

  • Forecast tooling and equipment obsolescence and develop mitigation strategies.

  • Manage retirement, documentation updates, and traceability controls for decommissioned tools.

Data Analytics & Continuous Improvement

  • Provide organizational expertise in:

    • OOT investigation trends

    • Mean Time Between Failures (MTBF)

    • Predictive maintenance strategies

    • System and tool capability (CpK)

    • Service performance metrics

    • Drive continuous improvement through data-driven insights.

Regulatory & Quality System Compliance

  • Develop, maintain, and enforce SOPs, work instructions, and records related to equipment control.

  • Serve as the audit liaison for test equipment management during MDSAP, FDA, and notified body audits.

  • Maintain regulatory surveillance and update policies in accordance with evolving standards.

Required Experience & Qualifications

  • Extensive experience managing test equipment and calibration programs in a regulated medical device environment.

  • Demonstrated project management capability, including planning, executing, and delivering multi0phase tool and equipment initiatives on time and within scope.

  • Proven experience supporting regulatory inspections and leading audit walkthroughs.

  • Strong understanding of metrology concepts, equipment tolerances, uncertainty, and traceability.

  • Proficiency with electronic calibration management tools (e.g., SimplerQMS, Blue Mountain, MasterControl).

  • Advanced capability in data analysis using Power BI.

  • Strong organizational skills, attention to detail, and SOP documentation experience.

  • Effective communicator with cross-functional collaboration skills.

Preferred Skills

  • Knowledge of service processes for medical devices.

  • Experience specifying, qualifying, and validating measurement and test tools.

  • Familiarity with technical standards such as IEC 62353, IEC 60601, and ISO 14971.

  • Strong background in statistical process control and risk-based decision making.

  • Experience with ERP integration and digital document control systems.

Why Join Us?

  • Impact patient safety and device reliability across global service operations.

  • Lead a critical compliance function with visibility across engineering, quality, and service teams.

  • Drive innovation in data analytics, tooling strategy, and operational excellence.

Required Skills:

Preferred Skills:

Agile Manufacturing, Coaching, Computer Programming, Continuous Improvement, Critical Thinking, Good Manufacturing Practices (GMP), Industry Analysis, Innovation, Plant Operations, Predictive Analytics, Process Improvements, Project Reporting, Prototyping, Quality Assurance (QA), Repair Management, Robotic Automation, Service Request Management, Technical Credibility

The anticipated base pay range for this position is :

Salary Range $118,000 - $203,550 Bay Area Only

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are 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. Subject to the terms of their respective plans, employees are eligible to participate in the Company0s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation 120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year Holiday pay, including Floating Holidays 13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

Johnson & Johnson Careers

Joining Johnson & Johnson provides an unparalleled opportunity to be a part of a global team of professionals dedicated to blending care, science, and innovation to profoundly change the trajectory of health for humanity.

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At Johnson & Johnson, you will engage in work that matters. Join our community of professionals in health care to drive significant and impactful changes across the globe. Our team at Johnson & Johnson leads with science and heart in sectors from pharmaceuticals to medical devices and consumer health products.

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Our team at Johnson & Johnson thrives on collaboration and diversity. You will work alongside over 130,000 employees globally who are committed to making a lasting impact. With a culture that values diversity training and leadership, you are supported in both personal and professional growth.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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