Senior Pharma Maintenance & Reliability Lead

Clutch Canada

United States

On-site

USD 90,000 - 125,000

Full time

14 days+
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Job summary

Liquidia is a leading biopharmaceutical company focused on developing therapies with innovative manufacturing and maintenance processes. The Maintenance Specialist ensures reliability, compliance, and lifecycle management of equipment, facilities, and utilities within a GMP environment, partnering with Engineering, Validation, Manufacturing, Quality, and Facilities.

Responsibilities include CMMS administration, maintenance planning, and participation in design reviews, FAT/SAT activities,

Qualifications

  • B.S. degree in Engineering, Maintenance or related field with 8+ years of relevant experience.
  • High School diploma with 12+ years of hands-on experience in pharmaceutical facilities or equipment maintenance.
  • Experience with CMMS platforms and asset lifecycle management.
  • Understanding of GMP regulations and pharmaceutical manufacturing.

Responsibilities

  • Review Engineering Turnover Packages to ensure maintenance readiness before asset acceptance.
  • Coordinate asset induction and enrollment into the CMMS.
  • Maintain preventive and predictive maintenance programs and optimize reliability.
  • Support regulatory inspections and internal audits; ensure GMP compliance.
  • Drive continuous improvement initiatives and lifecycle management of assets.

Skills

Maintenance planning
Analytical troubleshooting
Project management
Regulatory awareness
Communication

Education

B.S. in Engineering or related field
12+ years hands-on pharma facilities experience (high school diploma route)

Tools

CMMS software (Maximo, SAP PM, Oracle)

Job description

Liquidia is a leading biopharmaceutical company focused on developing therapies with innovative manufacturing and maintenance processes. The Maintenance Specialist ensures reliability, compliance, and lifecycle management of equipment, facilities, and utilities within a GMP environment, partnering with Engineering, Validation, Manufacturing, Quality, and Facilities.

Responsibilities include CMMS administration, maintenance planning, and participation in design reviews, FAT/SAT activities,

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