Facility Maintenance Engineer

Facility Maintenance Engineer

Position Summary:

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture.  The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.

Catalent Pharma Solutions in Kansas City, MO is hiring a Facility Maintenance Engineer. The Facilities Maintenance Engineer is a member of the Facilities Engineering Team and reports directly to the site head of facilities.  The position is responsible for maintaining and remodeling existing facilities and utilities, coordinating capital projects, and providing engineering support to the site maintenance department.  This position will have a strong focus on continuous improvement of facility and utility equipment achieved through project identification and execution.

This is a full-time, salary role.   This is onsite.  This position is a 1st Shift role with flexibility on the weekends.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. 

The Role:

• Maintenance Management: Leading the life cycle management and maintenance of critical systems (HVAC, electrical, plumbing, cleanrooms, mechanical spaces) to ensure they are functioning efficiently, safely, and in compliance with pharmaceutical standards
• Project Management: Planning and executing projects related to the expansion, renovation, or upgrades of pharmaceutical manufacturing facilities, including budgeting, scheduling, and ensuring compliance with Good Manufacturing Practices (GMP)
• Safety Compliance: Ensuring that the facility complies with all relevant health, safety, and environmental regulations and standards, including those specific to the handling and manufacturing of pharmaceuticals
• Quality Compliance: Leading investigation and resolution of issues resulting from utility, facility, and/or equipment malfunctions
• Vendor Management: Selecting and managing contractors and service providers for maintenance, security, cleaning, and other services, ensuring they meet the site requirements
• Emergency Planning: Developing, implementing, and executing emergency plans and procedures, including evacuation plans, to respond to emergencies, such as weather events, utility disruptions, chemical spills, etc
• Space Management: Optimizing the use of space within the facility, including planning for future space requirements, cleanroom standards, and segregation of different manufacturing operations
• Building Systems Design and Analysis: Assessing the design and operation of building systems to improve efficiency, reliability, and sustainability
• Regulatory Compliance: Ensuring that the facility and its operations comply with all local, state, federal, and international regulations and codes relevant to pharmaceutical manufacturing, including GMP and FDA regulations
• Sustainability Initiatives: Leading efforts to make the facility more sustainable, such as implementing recycling programs, reducing energy consumption and cost, water conservation measures, and green building practices, while ensuring these initiatives do not compromise product quality or safety
• All other duties as assigned

The Candidate:

• Bachelor’s Degree in Mechanical, Electrical or Chemical Engineering with a at least two years of relevant of experience in development, manufacturing or packaging for clinical/commercial drug products or