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Sobre esta vaga de Principal Facilities Engineer na Integra LifeSciences

Integra LifeSciences · Presencial · US-MA-Braintree-220-Facility

Changing lives. Building Careers.
 

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

The Principal Facility Engineer serves as the senior technical authority for the Integra LifeSciences Braintree manufacturing facility, providing leadership and oversight for facility infrastructure, utilities, maintenance engineering, capital projects, and continuous improvement initiatives that support medical device manufacturing operations. This role is responsible for ensuring the reliability, compliance, safety, and operational effectiveness of all building systems, manufacturing support utilities, and facility assets.


The Principal Facility Engineer leads complex capital and infrastructure projects while providing advanced troubleshooting expertise for electrical, electronic, mechanical, automation, HVAC, and utility systems. The position serves as a key partner to Operations, Quality, Validation, EHS, Supply Chain, and Corporate Engineering teams to ensure regulatory compliance, uninterrupted manufacturing operations, and achievement of site business objectives.


Additionally, the role leads facility-related non-conformance investigations, root cause analyses, and CAPA activities, utilizing structured problem-solving methodologies to drive sustainable corrective actions and continuous improvement throughout the site.



Essential Responsibilities

Facility Engineering & Infrastructure Management

  • Provide technical leadership for the operation, maintenance, reliability, and continuous improvement of facility infrastructure and manufacturing support systems.
  • Manage and support:
    • Electrical distribution systems
    • Emergency generators and UPS systems
    • HVAC and environmental control systems
    • Building Automation Systems (BAS/BMS)
    • Compressed air systems
    • Mechanical utility systems
    • Domestic water and plumbing systems
  • Develop long-range facility master plans, asset replacement strategies, and infrastructure improvement roadmaps.
  • Ensure facility systems meet operational requirements while maintaining compliance with regulatory and corporate standards.
  • Support business continuity planning and risk mitigation activities for critical facility infrastructure.

Advanced Electrical, Electronic & Mechanical Troubleshooting

  • Serve as the site's primary technical expert for diagnosing and resolving complex facility and manufacturing support system failures.
  • Troubleshoot electrical systems including:
    • Electrical distribution panels
    • Transformers
    • Generators
    • UPS systems
    • Static Invertors
    • Power monitoring systems
  • Troubleshoot electronic and automation systems including:
    • PLCs
    • Human Machine Interfaces (HMIs)
    • Sensors and instrumentation
    • Building automation controls
    • Environmental monitoring systems
    • Variable Frequency Drives (VFDs)
    • Networked control systems
  • Troubleshoot mechanical systems including:
    • HVAC equipment
    • Chillers
    • Boilers
    • Air handling units
    • Pumping systems
    • Compressed air equipment
    • Hydraulic and pneumatic systems
    • Lyophilization equipment
  • Lead recovery efforts during critical equipment failures and utility interruptions.
  • Analyze recurring failures and implement permanent engineering solutions to improve reliability and uptime.

Capital Project & Program Management

  • Lead facility capital and expense projects from concept development through commissioning and project closeout.
  • Develop project charters, scopes of work, budgets, schedules, risk assessments, and resource plans.
  • Manage multiple concurrent facility engineering projects supporting manufacturing operations and site growth.
  • Coordinate activities of contractors, consultants, architects, equipment suppliers, and engineering service providers.
  • Oversee facility renovations, infrastructure upgrades, equipment installations, utility expansions, and modernization initiatives.
  • Monitor project performance to ensure completion on schedule, within budget, and in compliance with safety and quality requirements.
  • Prepare and present project updates, business cases, and financial justifications to site and corporate leadership.
  • Support commissioning, qualification, validation, and startup activities for new facility systems and equipment.

Non-Conformance, CAPA & Quality System Leadership

  • Lead investigations related to facility, utility, infrastructure, environmental, equipment, and maintenance-related non-conformances, deviations, and quality events.
  • Serve as the Facility Engineering Subject Matter Expert during quality investigations and regulatory assessments.
  • Conduct comprehensive root cause investigations utilizing structured methodologies including:
    • Root Cause Analysis (RCA)
    • 5-Why Analysis
    • Fishbone (Ishikawa) Analysis
    • Failure Mode and Effects Analysis (FMEA)
    • Fault Tree Analysis (FTA)
    • Cause Mapping
  • Assess impact to manufacturing operations, product quality, environmental controls, and regulatory compliance.
  • Develop and implement corrective and preventive actions (CAPAs) designed to eliminate recurrence and improve system reliability.
  • Partner with Quality Assurance, Operations, Validation, Manufacturing Engineering, and EHS teams to establish effective containment and corrective action plans.
  • Author investigation reports, engineering assessments, risk analyses, CAPA documentation, and effectiveness checks.
  • Verify effectiveness of corrective actions through data analysis, system performance monitoring, and trend evaluations.
  • Drive continuous improvement initiatives to reduce repeat failures, utility interruptions, maintenance issues, and facility-related quality events.
  • Support internal audits, customer audits, FDA inspections, and ISO certification activities.

Regulatory Compliance & Risk Management

  • Ensure compliance with:
    • FDA Quality System Regulations (21 CFR Part 820)
    • ISO 13485 requirements
    • OSHA regulations
    • NFPA standards
    • National Electrical Code (NEC)
    • Environmental regulations
    • Corporate engineering standards
  • Support change control, validation, commissioning, qualification, and maintenance documentation processes.
  • Maintain engineering drawings, equipment records, specifications, PM procedures, and technical documentation.
  • Participate in risk assessments and mitigation planning for critical facility systems and utilities.

Reliability & Continuous Improvement

  • Implement preventive, predictive, and reliability-centered maintenance strategies.
  • Analyze facility performance metrics and equipment reliability trends.
  • Develop and monitor KPIs related to:
    • CAPA effectiveness
    • Maintenance performance
    • Project execution
  • Lead energy conservation and sustainability initiatives.
  • Apply Lean Manufacturing and continuous improvement principles to optimize facility performance and reduce operating costs.
  • Mentor maintenance personnel, facilities technicians, and junior engineers.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, Facilities Engineering, or related engineering discipline.
  • Minimum 10 years of progressive experience in facility engineering, manufacturing engineering, maintenance engineering, or infrastructure management.
  • Minimum 5 years of experience managing capital projects and cross-functional engineering initiatives.
  • Extensive experience troubleshooting electrical, electronic, automation, and mechanical systems in a manufacturing environment.
  • Experience with HVAC systems, utilities, building automation systems, power distribution, and industrial controls.
  • Demonstrated experience conducting root cause investigations and managing CAPA activities.
  • Strong understanding of FDA-regulated or ISO-certified manufacturing environments.
  • Excellent leadership, project management, communication, and organizational skills.

Preferred Qualifications

  • Certified Reliability Engineer (CRE) certification.
  • Experience within medical devices, pharmaceutical, biotechnology, or other highly regulated manufacturing industries.
  • Experience with CMMS platforms, BAS/BMS systems, environmental monitoring systems (EEMS), and computerized quality systems.

Core Competencies

  • Facility Engineering Leadership
  • Capital Project Management
  • Electrical System Troubleshooting
  • Electronic Controls & Automation Troubleshooting
  • Mechanical System Troubleshooting
  • HVAC & Utility Systems Management
  • Building Automation Systems
  • Root Cause Analysis
  • Non-Conformance Investigation
  • CAPA Management
  • FMEA & Risk Assessment
  • Reliability Engineering
  • Regulatory Compliance
  • Contractor Management
  • Continuous Improvement
  • Strategic Planning
  • Cross-Functional Leadership

Success Measures

  • Safe and compliant operation of all facility infrastructure and utility systems.
  • Successful delivery of capital projects on time and within budget.
  • Reduction in facility and utility-related downtime events.
  • On-time closure of non-conformances, investigations, and CAPAs.
  • Demonstrated effectiveness of corrective actions and reduction of repeat events.
  • Improved equipment reliability and facility uptime.
  • Successful audit and regulatory inspection outcomes.
  • Achievement of energy efficiency, sustainability, and cost reduction objectives.

This position functions as the senior Facilities Engineering Subject Matter Expert for the Integra LifeSciences Braintree manufacturing site, combining engineering leadership, advanced troubleshooting expertise, quality systems ownership, and project management excellence to ensure a safe, compliant, reliable, and efficient manufacturing environment.

Salary Pay Range:

$125,350.00 - $172,500.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

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, and savings plan (401(k)).

 

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at [email protected].

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

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Sobre a Integra LifeSciences

Whatever your specialty, you’ll find an ideal setting for building a rewarding career. Along the way, you’ll have the satisfaction of knowing your work matters, that it’s making patients’ lives better, making a positive and lasting difference. You’ll find that the pace is exhilarating – because the need is so urgent. You’ll be challenged – and supported – by the most dynamic and inspiring people in your profession. And you’ll grow a career that is more impactful and fulfilling then you thought possible. More than 4,200 Integra employees already know we’re a great place to build a career. Here’s your chance to discover that for yourself.

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