Technician - Biomanufacturing, Central Services
Listed on 2026-07-13
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Manufacturing / Production
Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Production QC/QA
Technician - Biomanufacturing, Central Services Position Summary
- Work Schedule:
6am-4pm (Sunday-Wednesday or Wednesday–Saturday shift availability) - 100% on-site
Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). 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. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.
This is an entry-level position in the Manufacturing team and is the starting point to acquiring skills and training required for a cGMP biomanufacturing environment. The Technician is responsible for the manufacture of biopharmaceutical products within a clean room environment. The position is expected to follow detailed instructions and established procedures with frequent supervision.
The Role- Perform basic buffer preparation activities, including weighing raw materials for production
- Accurately follow manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) with a focus on “right first time” execution
- Document all activities in accordance with Good Documentation Practices (GDPs) in BPRs, forms, and other quality documentation
- Recognize deviations from the intended procedure and raise awareness through the Rapid Response process
- Proactively identify safety, quality, and efficiency improvements; actively participate in the Catalent Way (Continuous Improvement Culture)
- May lead “Just Do It” (JDI) Continuous Improvement (CI) activities and engage in implementation of CI projects
- May coach more junior team members on basic execution activities and act as an “onboarding buddy” to facilitate bringing new team members quickly up to speed on culture and basic workplace expectations
- Perform general cleanroom housekeeping, including room and equipment cleaning, disposal of waste, and maintenance of 5S standards
- Other duties as assigned
- Must have High School Diploma or equivalent. No additional experience required
- GMP manufacturing experience preferred
- Ability to use Microsoft Word and Excel, and other Office systems
- Preferred experience with Track Wise, Compliance Wire, JD Edwards, DeltaV, Chromatography software
- Physical requirements:
frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening; occasional stooping, kneeling, crouching, bending, carrying, grasping; frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds; must comply with EHS responsibilities for the position; working conditions will be HVAC controlled; ability to operate within a clean room environment as needed
- 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
Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by email to Disabili Please include the job number, title and location.
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