Catalent, Inc.

Biomanufacturing

BiomanufacturingTechnician,CentralServices

$48–65k ~AI est. Madison, Wisconsin, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Biomanufacturing Technician, Central Services at Catalent, Inc.. Skills: Biomanufacturing, cGMP, Documentation. Perform basic buffer preparation. Weigh raw materials for production”

Industry & Context.

Biomanufacturing
Problems you'll solve

Root cause analysis

Eligibility Requirements

Lifting up to 10 pounds, Lifting up to 50 pounds, Work within a clean room

What They're Looking For.

Must Have

High School Diploma or equivalent, Ability to use Microsoft Word and Excel, Ability to use other Office systems

Nice to Have

GMP manufacturing experience, Experience with TrackWise, Experience with ComplianceWire, Experience with JD Edwards, Experience with DeltaV, Experience with Chromatography software

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

Identify safety issues

Identify quality issues

Identify 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

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: 2pm-12am Wednesday – Saturday * 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 speed on culture and basic workplace expectati

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