Facilities Specialist
Catalent
Summary
We have an opportunity for a Facilities Specialist to join our team as part of the Facilities and Engineering group. In this role, you will help maintain facilities, equipment, and instruments to ensure reliable operation. You will perform a variety of maintenance activities, such as painting, carpentry, and support for HVAC installations, while following all health and safety requirements. This position offers the chance to work both independently and collaboratively to keep our buildings and common areas in optimal condition.
Job description
Position Summary
We have an opportunity for a Facilities Specialist to join our team as part of the Facilities and Engineering group. In this role, you will help maintain facilities, equipment, and instruments to ensure reliable operation. You will perform a variety of maintenance activities, such as painting, carpentry, and support for HVAC installations, while following all health and safety requirements. This position offers the chance to work both independently and collaboratively to keep our buildings and common areas in optimal condition.
Shift: Monday - Friday, 8am-5pm. Location: Princeton, NJ 100% Onsite.
The Role
- Perform routine and preventive maintenance on buildings and equipment, including basic plumbing, electrical, and HVAC work, and escalate complex issues to the Facilities and Engineering Team.
- Provide hands-on maintenance, repair, and support to meet business needs.
- Respond to housekeeping requests and perform in-house repairs throughout the facility and grounds.
- Document completed service requests in the Work Order Management System.
- Perform equipment administration tasks, including processing authorized user access requests and completing password resets in accordance with approved procedures and access controls.
- Monitor the Building Automation System (BAS) and Environmental Monitoring System (EMS) daily, and promptly report alarms, deviations, and system issues to the Facilities and Engineering Team.
- Apply an understanding of lockout/tagout (LOTO) requirements when performing assigned work.
- Perform facility maintenance and housekeeping activities, including cleaning, painting, basic electrical and mechanical troubleshooting, and upkeep of equipment, furniture, fixtures, and building systems.
- Work effectively both independently and as part of a team.
- Complete paperwork and assigned projects accurately and on time.
- Perform other duties as assigned.
The Candidate
Minimum Requirements
- High School Diploma or GED required.
- 3+ years of related experience in biologics manufacturing, Good Manufacturing Practice (GMP) environment, hospital, food, or chemical industries.
- Able to communicate effectively in English with supervisors, other technicians, and contractors.
- Basic math and computer skills (Microsoft Word, Microsoft Excel) and familiarity with building automation systems (BAS).
- Good mechanical ability for troubleshooting and repairing equipment.
- Must be able to clearly communicate in English, both verbally and in writing.
- Maintain reliable attendance and be available to work extended hours or report on short notice, as required.
- Ability to perform both office- and field-based responsibilities, including extended periods of sitting, standing, walking, data/document preparation, equipment inspection, and operation within industrial manufacturing environments.
- Ability to safely lift and move up to 50 pounds, work in confined spaces and at elevated locations, utilize required PPE, and tolerate exposure to noise, vibration, temperature fluctuations, and other industrial conditions while performing maintenance and operational activities.
Preferred Skills & Background
- Basic understanding of mechanical and electrical systems in a biopharmaceutical manufacturing or research and development facility that supports GMP production of Phase I/II bulk biologics preferred.
- Experience working in an FDA-regulated cleanroom environment that requires full gowning, including a Tyvek coverall, gloves, hair cover, and shoe covers preferred.
Requirements
- High School Diploma or GED required
- 3+ years of related experience in biologics manufacturing, GMP environment, hospital, food, or chemical industries
- Able to communicate effectively in English with supervisors, other technicians, and contractors
- Basic math and computer skills (Microsoft Word, Microsoft Excel)
- Familiarity with building automation systems (BAS)
- Good mechanical ability for troubleshooting and repairing equipment
- Must be able to clearly communicate in English, both verbally and in writing
- Maintain reliable attendance and be available to work extended hours or report on short notice
- Ability to perform office- and field-based responsibilities including sitting, standing, walking, and equipment inspection
- Ability to safely lift and move up to 50 pounds, work in confined spaces and at elevated locations, utilize required PPE, and tolerate industrial conditions
Benefits
- Medical, Dental & Vision
- Paid Time Off
- 8 Paid Holidays
- Tuition Reimbursement
- Annual Performance Review
- Career Growth Opportunities
- Community Engagement Initiatives
Company overview
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) that serves as a trusted partner to pharmaceutical, biotech, and consumer health companies worldwide. Founded on a legacy dating back to 1933, Catalent has evolved into a comprehensive drug development and delivery leader with over 40 global sites. The company specializes in providing end-to-end solutions spanning oral dose formulations, biologics, specialty products, and clinical supply services. Catalent's expertise includes formulation development, analytical services, commercial manufacturing, and advanced delivery technologies such as Zydis® fast-dissolve tablets and softgel technologies. With over 1,000 active development programs at any given time, the company launches more than 100 new products and line extensions annually and has supported half of all FDA approvals over the past decade. Catalent produces over 60 billion treatment doses per year, helping approximately 200 million patients annually. Headquartered in Tampa, Florida, the company employs more than 10,000 professionals globally who are dedicated to putting patients first and championing the missions that matter in healthcare innovation.