Technician- Biomanufacturing, Upstream

Position Summary

Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this 263,000 sq. ft. Good Manufacturing Practice (GMP) facility supports advanced mammalian cell line engineering and biomanufacturing capabilities using single‑use systems for scalable biopharmaceutical production. The Technician role is an entry‑level position in the Manufacturing team, providing the foundation for cGMP biomanufacturing experience. Work schedule is 6 am‑4 pm, with shift availability on Sunday‑Wednesday or Wednesday‑Saturday.

The Technician works 100 % on‑site in a Grade A cleanroom environment and follows detailed instructions and procedures with frequent supervision.

• Perform basic upstream cell culture activities, including aseptic manipulation of cell culture within a Grade A environment, large‑scale culture within single‑use bioreactors, and clarification of bulk harvest product.
• Accurately follow manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs).
• 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” 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.
• Perform general cleanroom housekeeping, including room and equipment cleaning, waste disposal, and maintenance of 5S standards.
• Other duties as assigned.

• High School Diploma or equivalent with at least two (2) years of relevant experience, or a Bachelor’s or Associate’s Degree in a scientific, engineering, or biomanufacturing discipline without formal experience.
• GMP manufacturing experience preferred.
• Ability to use Microsoft Word, Excel, and other Office system applications.
• Preferred experience with Track Wise, Compliance Wire, JD Edwards, DeltaV, or chromatography software.
• Physical requirements:
  
  frequent sitting, standing, walking, reading, using a computer monitor, reaching, talking, writing, listening; occasional stooping, kneeling, crouching, bending, carrying; frequent lifting and/or moving up to 10 lb, occasional lifting up to 50 lb; ability to operate within a cleanroom environment and comply with EHS responsibilities; heating, ventilation, and air‑conditioning controlled conditions.

• Defined career path with annual performance reviews and feedback.
• Diverse, inclusive culture.
• Potential for career growth on an expanding team.
• 152 hours of PTO plus 8 paid holidays.
• Generous 401(k) match.
• Medical, dental, and vision benefits.
• Tuition reimbursement opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.