C

Curia

End-to-end drug development and manufacturing

Manager Maintenance

Equipment MaintenanceConfirmed live in the last 24 hours
Full-timeSpringfield, MO, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering or a related field is required.
  • At least five years of relevant work experience and two years in a team leadership role are required.
  • Candidates must pass a background check and drug screen; an occupational health screening may also be required.
  • The role requires physical ability to regularly stand, walk, communicate, and handle equipment, tools, and materials; it may require occasional climbing, balancing, stooping, kneeling, confined or elevated-space work, and lifting or moving up to 50 pounds.
  • Candidates must be medically fit to wear a respirator.
  • Ability to read and interpret equipment manuals, mechanical blueprints, and P&IDs.
  • Proficiency in Microsoft Office Suite and Computerized Maintenance Management System (CMMS) platforms.
  • Knowledge of safety regulations and Food and Drug Administration Good Manufacturing Practice requirements applicable to pharmaceutical chemical manufacturing.
  • Strong organizational skills and ability to manage multiple projects concurrently.

Responsibilities

  • Provide day-to-day leadership of all maintenance and utilities functions for a 24/7 pharmaceutical chemical manufacturing facility.
  • Oversee repair and maintenance activities for facility and equipment to meet safety, current Good Manufacturing Practice compliance, and cost-effectiveness priorities.
  • Optimize preventive and predictive maintenance programs to minimize unplanned downtime and reduce out-of-service time.
  • Implement systematic planning and scheduling processes that use human and financial resources effectively.
  • Set strategic direction for long-term equipment reliability and high uptime.
  • Lead, motivate, and develop a team of multi-skilled maintenance technicians, supporting their growth, performance, and productivity.
  • Create a work environment that supports skills development and career advancement.
  • Measure performance and provide feedback through periodic reviews.
  • Ensure staff receive appropriate documented training before being assigned work.
  • Partner with Engineering, EHS, Operations, Warehouse, and Quality on facility maintenance, repair, and related project decisions.
  • Develop and manage the departmental budget through cost estimation and control.
  • Develop and communicate goals and standards and ensure activities comply with DEA, FDA, EPA, OSHA, and other applicable regulations.
  • Escalate quality concerns to the Quality department with proposed compliant solutions.
  • Perform work in alignment with current Good Manufacturing Practice requirements and company standards.
  • Promote a quality-first culture for work performed.
  • Complete documentation in compliance with ALCOA+ principles and site standard operating procedures.
  • Follow applicable current Good Manufacturing Practice documents, including standard operating procedures, batch records, protocols, change controls, and controlled forms.
  • Keep required current Good Manufacturing Practice training current for self and team, and escalate quality concerns with proposed solutions to the Quality department.
  • Support broader site and business needs as reasonably assigned.
  • Work in an office or maintenance shop and regulated pharmaceutical chemical manufacturing environment, with regular exposure to fumes, airborne particles, low levels of toxic or caustic chemicals with required personal protective equipment, wet or humid conditions, moving mechanical parts, elevated or precarious places, elevated noise, extreme heat, and electrical-shock risks; outdoor work and varied weather exposure may also occur.

Desired Qualifications

  • Experience in a pharmaceutical or regulated manufacturing environment is strongly preferred.
  • Formal education and/or training in engineering or industrial technology; a bachelor's degree is preferred.
  • Experience with predictive and preventive maintenance strategies and Computerized Maintenance Management Systems; SAP experience is a plus.
  • Working knowledge of chemical manufacturing equipment, including pumps, mixers, reactors, electrical systems, process control systems, and utility systems such as boilers, compressed air, and refrigeration.
  • Strong leadership skills demonstrated by mentoring, developing, and inspiring multi-skilled teams.
  • Ability to engage technically and influence cross-functionally across a complex, regulated site.
  • Communication and negotiation skills for engaging technical and non-technical audiences.
  • Ability to recognize what needs to be done, take initiative, and drive results with urgency and integrity.
  • Ability to manage competing priorities and coordinate resources effectively.

About the Company

Curia

End-to-end drug development and manufacturing

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Albany, NY
Founded
1991

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