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Fujifilm

Global precision manufacturer for healthcare

Associate Director / Director Maintenance

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeHolly Springs, NC, USANo salary listedIn-person

About the Job

Requirements

  • Demonstrated ability to build a high-performing technical organization through high-quality one-on-ones, actionable feedback, individualized development plans, strategic workforce planning, competency frameworks, succession planning, and retention strategies.
  • Ability to effectively lead and coach a maintenance and calibration team of 40 or more personnel within a matrixed organization.
  • Ability to build trust with cross-functional peers and resolve issues and conflicting priorities through partnership, negotiation, and clear decision frameworks.
  • Ability to drive core team culture priorities, including safety, GEMBA, leadership principles, and cost consciousness, into ways of working.
  • Ability to work in a fast-paced, uncertain, and shifting environment while managing multiple tasks and projects simultaneously.
  • In-depth knowledge of current Good Manufacturing Practice requirements applicable to equipment maintenance and computerized systems in biopharmaceutical manufacturing, including 21 CFR 211.67, 21 CFR Part 11, and EU Good Manufacturing Practice, and ability to defend the maintenance program during inspections.
  • Working knowledge of reliability and asset management methodologies, including criticality analysis, reliability-centered maintenance, failure mode and effects analysis, condition-based maintenance technologies, root cause failure analysis, and ISO 55000 principles.
  • Experience implementing or governing an enterprise computerized maintenance management system, such as SAP PM, Maximo, or Blue Mountain, including equipment master data, work management, and materials management.
  • Strong technical knowledge of biopharmaceutical process and utility equipment, including bioreactors, chromatography and filtration skids, clean-in-place/steam-in-place systems, water for injection and clean steam systems, heating, ventilation and air conditioning, chillers, and boilers.
  • Proven ability to build maintenance programs and organizations in a startup or ramp-up environment, establishing processes, procedures, and controls where they do not yet exist.
  • Ability to apply risk-based decision-making, including ICH Q9(R1), and use data to prioritize resources, justify program changes, and communicate trade-offs to senior leadership.
  • Strong financial acumen, including budget development, cost control, and spare parts inventory management.
  • Must be flexible to support a 24/7 manufacturing facility.
  • Bachelor's degree in life science, engineering, or a related field with 8 to 10 or more years of related experience, or a master's degree in life science, engineering, or a related field with 6 or more years of experience in a similar role.
  • At least 4 years of experience leading and developing leaders, such as managers and supervisors, and leading and developing people.
  • Experience working in a changing, project-driven organization.
  • Prior experience using an enterprise computerized maintenance management system, such as SAP PM, Maximo, or Blue Mountain, to manage work orders, preventive maintenance plans, and maintenance records.

Responsibilities

  • Empower, lead, and develop a high-performing, multi-disciplined team of leaders and technicians through servant leadership, fostering a People First culture and continuous learning and development through real-time feedback, coaching, mentoring, and succession planning.
  • Ensure team members are strategically placed in positions and on projects where their skills are effectively utilized and challenged, while promoting individual growth and organizational productivity.
  • Establish and govern the site work management process, including work identification, prioritization, planning, scheduling, backlog management, and schedule compliance, coordinating equipment access and maintenance windows with manufacturing.
  • Own the maintenance systems strategy, including the computerized maintenance management system as the system of record for equipment master data, work orders, preventive maintenance plans, and spare parts, ensuring data integrity (ALCOA+) and compliant use of electronic records.
  • Sponsor the site reliability program and ensure equipment criticality assessment, reliability-centered maintenance, condition-based maintenance, mechanical integrity, and root cause failure analysis are deployed and translated into defensible maintenance strategies.
  • Direct the spare parts program, including critical spares identification, a risk-based stocking strategy accounting for equipment criticality and inventory value, storeroom controls, and repair and return processes, in partnership with supply chain and procurement.
  • Develop and execute the maintenance ramp-up plan in support of site capacity growth, including organizational design, headcount and hiring plans, shift coverage models, onboarding newly turned-over equipment into the maintenance program, and readiness criteria for commercial operation.
  • Govern the preventive maintenance program lifecycle, ensuring maintenance content and interval changes are risk-assessed, supported by trended performance data, and implemented through formal change control.
  • Ensure the maintenance program complies with current Good Manufacturing Practice requirements through controlled procedures, change control, deviation and corrective and preventive action management, and equipment return-to-service controls; represent Maintenance during regulatory inspections, customer audits, and internal audits.
  • Define and report maintenance and reliability performance indicators, including schedule and preventive maintenance compliance, backlog, equipment availability, mean time between failures, and deviations, and lead maintenance business reviews with site leadership.
  • Develop and manage the maintenance operating budget, including labor, contracted services, materials, and spare parts inventory value, and contribute to capital planning and lifecycle replacement decisions.
  • Oversee contracted maintenance service providers and original equipment manufacturers, including scope definition, onboarding, performance management, and documented oversight consistent with current Good Manufacturing Practice and environmental, health, and safety expectations.
  • Champion a strong safety culture and ensure compliance with environmental, health, and safety requirements, including hazardous energy control (lockout/tagout), permit-to-work, and contractor safety.
  • Build and maintain strong partnerships with internal and external stakeholders, including Manufacturing, Quality, and Validation, to collaborate on maintenance and calibration projects and deliver high-quality support.
  • Evaluate team performance, develop and implement measures to improve productivity and engagement, and partner with People & Culture to recruit, retain, and develop talent.
  • Perform other duties as assigned.

Desired Qualifications

  • Bachelor's degree in life science, engineering, or a related field with 10 or more years of related experience, or a master's degree in life science, engineering, or a related field with 8 or more years of experience in a similar role.
  • At least 6 years of experience managing, leading, and developing people.
  • Six to ten years of experience in pharmaceutical or biological manufacturing operations.
  • Experience leading maintenance through a new facility startup, commissioning and qualification, or ramp-up to commercial manufacturing.
  • Prior experience deploying a computerized maintenance management system, reliability program, or spare parts program within a regulated manufacturing environment.

About the Company

Fujifilm

Global precision manufacturer for healthcare

Fujifilm is the main operating and manufacturing arm of the Fujifilm group, turning precision chemistry, nanotechnology, and optical engineering from the film era into products for deep tech and life sciences. It runs Bio CDMO facilities that manufacture complex biopharmaceuticals and vaccines, and its materials division makes photoresists and chemical slurries essential to semiconductor and display production. In healthcare, it develops AI-powered imaging devices, endoscopes, and ultrasound systems, while also serving consumers with INSTAX instant photos and X-Series cameras. Its goal is to translate core technical capabilities into reliable, market-ready products across healthcare, electronics materials, and imaging, maintaining leadership in precision manufacturing and applied science.

Company size
501-1,000
Company stage
IPO
Headquarters
Tokyo, Japan
Founded
1934

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