Catalent, Inc.
Biomanufacturing
BiomanufacturingTechnician,CentralServices
Neural analysis suggests this role is
optimal for Entry candidates.
“Biomanufacturing Technician, Central Services at Catalent, Inc.. Skills: Biomanufacturing, cGMP environment. Perform basic buffer preparation. Weigh raw materials for production”
Industry & Context.
Root cause analysis
Frequent sitting, standing, walking, Reading of written documents, Use of computer monitor screen, Reaching with hands and arms, Talking, writing, listening, Occasional stooping, kneeling, crouching, Occasional bending, carrying, grasping, Lifting up to 10 pounds, Lifting up to 50 pounds, EHS responsibilities, Operate within clean room
What They're Looking For.
Must Have
High School Diploma or equivalent, No additional experience required
Nice to Have
GMP manufacturing experience preferred, Experience with TrackWise preferred, Experience with ComplianceWire preferred, Experience with JD Edwards preferred, Experience with DeltaV preferred, Experience with Chromatography software preferred
What You'll Do.
Perform basic buffer preparation
Weigh raw materials for production
Follow manufacturing Batch Production Records
Follow Standard Operating Procedures
Document all activities
Recognize deviations from procedure
Raise awareness through Rapid Response
and efficiency issues
Participate in Catalent Way
Lead "Just Do It" activities
Engage in CI project implementation
Coach junior team members
Act as onboarding buddy
Perform general cleanroom housekeeping
Clean room and equipment
Maintain 5S standards
How You'll Work.
Team & Collaboration
Junior team members; New team members
Process & Methodology
Continuous Improvement
Full Job Description
**Biomanufacturing Technician, Central Services** **Position Summary:** * Work Schedule: 10pm-8am (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 follows manufacturing Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) and with a focus on “right first time” execution * Documents all activities in accordance with Good Documentation Practices (GDPs) in BPRs, Forms, and other quality documentation * Recognizes deviations from the intended procedure and raises awareness through the Rapid Response process * Proactively identifies safety, quality, and efficiency improvements; Actively participates 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 spe
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