Entry-Level Biomanufacturing Technician (GMP Cleanroom)

Catalent

Madison (WI)

On-site

USD 36,000 - 48,000

Full time

6 days ago
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Benefits offered by this job

152 hours of PTO + 8 paid holidays
Generous 401K match
Medical, dental and vision benefits
Tuition Reimbursement

Job summary

Catalent, Inc. in Madison, WI, is hiring an entry-level Manufacturing Technician to join a GMP biomanufacturing facility.

You will work 2pm-12am, Sunday through Wednesday, 100% on-site, supporting the manufacture of biopharmaceutical products in a clean room and following BPRs and SOPs with supervision. Key duties include basic buffer preparation, material weighing, GDP-compliant documentation, deviations handling, and contributing to CI initiatives.

Qualifications

  • High School Diploma or equivalent.
  • GMP manufacturing experience preferred.
  • Ability to use Word and Excel and other Office systems.
  • Experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, or chromatography software is a plus.
  • Comfort with following detailed instructions in a cleanroom environment.

Responsibilities

  • Perform basic buffer preparation activities, including weighing raw materials for production.
  • Follow Batch Production Records and SOPs in accordance with cGMPs.
  • Document activities in GDP-compliant records and forms.
  • Identify deviations and escalate through Rapid Response.
  • Contribute to safety, quality, and efficiency improvements; participate in CI projects.
  • May coach junior team members and assist onboarding.
  • Maintain cleanroom housekeeping and 5S standards.
  • Other duties as assigned.

Education

High School Diploma or equivalent

Tools

Microsoft Word
Microsoft Excel
TrackWise
ComplianceWire
JD Edwards
DeltaV
Chromatography software

Job description

Catalent, Inc. in Madison, WI, is hiring an entry-level Manufacturing Technician to join a GMP biomanufacturing facility.

You will work 2pm-12am, Sunday through Wednesday, 100% on-site, supporting the manufacture of biopharmaceutical products in a clean room and following BPRs and SOPs with supervision. Key duties include basic buffer preparation, material weighing, GDP-compliant documentation, deviations handling, and contributing to CI initiatives.

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