Entry-Level Biomanufacturing Technician - GMP On-Site

Catalent Pharma Solutions

Alabama

On-site

USD 42,000 - 54,000

Full time

6 days ago
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Benefits offered by this job

Defined career path and annual review
Generous 401K match
Medical, dental and vision benefits
Paid holidays and PTO

Job summary

Catalent, Inc. is hiring an entry-level Biomanufacturing Technician in a 2pm-12am on-site role at the Madison, WI facility. You will support biopharmaceutical production, follow BPRs, SOPs, and GDP documentation in a cleanroom environment, contributing to continuous improvement and ensuring safety and quality standards.

The position emphasizes training, adherence to GMP, and collaboration with a team to develop skills for a cGMP biomanufacturing setting.

Qualifications

  • 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 TrackWise, ComplianceWire, JD Edwards, DeltaV, Chromatography software.

Responsibilities

  • Perform basic buffer preparation activities, including weighing raw materials for production.
  • Follow Batch Production Records and SOPs per cGMP with right first time execution.
  • Document all activities in GDP-compliant records and forms.
  • Recognize deviations and raise issues via Rapid Response process.
  • Participate in Continuous Improvement and CI projects; may coach junior teammates.
  • Maintain cleanroom housekeeping and 5S standards; operate within controlled environment.

Skills

Attention to detail
Quality documentation
Safety awareness
Team collaboration

Education

High School Diploma or equivalent

Tools

TrackWise
ComplianceWire
JD Edwards
DeltaV
Chromatography software
Microsoft Excel
Microsoft Word

Job description

Catalent, Inc. is hiring an entry-level Biomanufacturing Technician in a 2pm-12am on-site role at the Madison, WI facility. You will support biopharmaceutical production, follow BPRs, SOPs, and GDP documentation in a cleanroom environment, contributing to continuous improvement and ensuring safety and quality standards.

The position emphasizes training, adherence to GMP, and collaboration with a team to develop skills for a cGMP biomanufacturing setting.

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