Technician I - Facilities, Equipment

Catalent•Madison, WI

3d•Onsite

About The Position

Technician I - Facilities, Equipment Position Summary: Work Schedule: Monday - Friday, 7:00am-3:30pm 100% on-site Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. site offers integrated formulation and analytical services to address complex development challenges in biologics. The Equipment Maintenance team works closely with both Maintenance and Calibration to directly support manufacturing and development equipment. This includes but is not limited to performing preventative maintenance in the clean room and lab environment and equipment troubleshooting, both in place and in a workshop space. The Equipment Maintenance Technician I is responsible for initial response to requests for support by manufacturing in the event of equipment problems. The Role: Follow general instructions on routine work and detailed instructions on new work Use hand tools, power tools, and delicate testing equipment in performance of duties Effectively document work performed following required documentation practices Perform basic troubleshooting as it related to assigned job duties Identify and order spare or replacement parts for equipment utilizing inventory management system Interact with other departments to schedule activities around the production schedules of the cGMP Manufacturing and Process Development departments Other duties as assigned The Candidate:

Requirements

Must have Technical or Associates Degree in a maintenance related field OR High School Diploma or GED and 2 years of relevant experience
1+ year’s in a manufacturing facility, preferably in a cGMP related environment is preferred
Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening is required
Occasional stooping, kneeling, crouching, bending, carrying, grasping is required
Frequent lifting and/or moving up to 25 pounds and occasional lifting and/or moving up to 50 pounds is required

Nice To Haves

1+ year’s in a manufacturing facility, preferably in a cGMP related environment is preferred

Responsibilities

Follow general instructions on routine work and detailed instructions on new work
Use hand tools, power tools, and delicate testing equipment in performance of duties
Effectively document work performed following required documentation practices
Perform basic troubleshooting as it related to assigned job duties
Identify and order spare or replacement parts for equipment utilizing inventory management system
Interact with other departments to schedule activities around the production schedules of the cGMP Manufacturing and Process Development departments
Other duties as assigned

Benefits

Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of PTO + 8 paid holidays
Generous 401K match
Medical, dental and vision benefits
Tuition Reimbursement - Let us help you finish your degree or start a new degree!
Catalent offers rewarding opportunities to further your career!
Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
Join us in making a difference.
personal initiative.
dynamic pace.
meaningful work.