Downstream/mRNA Biomanufacturing Technician (2nd Shift)

Ourlivesmadison

Alabama

On-site

USD 42,000 - 60,000

Full time

6 days ago
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Benefits offered by this job

PTO & holidays
401K match
Medical/dental/vision benefits
Tuition reimbursement

Job summary

Catalent, a leading global CDMO, is hiring an entry-level Technician – Biomanufacturing (Downstream/mRNA) at its Madison, WI facility. The role involves 2pm–12am shifts, 100% on-site, and working in a clean room environment within a GMP framework.

Responsibilities include IVT, chromatography, TFF, and chromatography-related tasks; strict adherence to BPRs/SOPs and GDPs; contributing to safety, quality, and continuous improvement efforts.”

Qualifications

  • Requires a high school diploma or equivalent with 2+ years in a related field or a Bachelor's/Associate degree in a scientific/engineering/biomanufacturing discipline.
  • GMP manufacturing experience is preferred.
  • Proficiency with Word/Excel and other Office systems; familiarity with related software is a plus.

Responsibilities

  • Perform downstream purification and mRNA production activities (IVT reactions, chromatography, TFF, viral filtration, column packing/qualification).
  • Follow Batch Production Records (BPRs) and SOPs in accordance with cGMPs, with emphasis on right first time execution.
  • Document activities per GDP in BPRs and quality documents; identify deviations and escalate via Rapid Response.
  • Support continuous improvement via Catalent Way and CI projects; may coach junior teammates.

Skills

MS Word & Excel proficiency
GMP manufacturing experience

Education

High School Diploma or equivalent
Bachelor's or Associate Degree in science/engineering/biomanufacturing

Tools

TrackWise
ComplianceWire
JD Edwards
DeltaV
Chromatography software

Job description

Catalent, a leading global CDMO, is hiring an entry-level Technician – Biomanufacturing (Downstream/mRNA) at its Madison, WI facility. The role involves 2pm–12am shifts, 100% on-site, and working in a clean room environment within a GMP framework.

Responsibilities include IVT, chromatography, TFF, and chromatography-related tasks; strict adherence to BPRs/SOPs and GDPs; contributing to safety, quality, and continuous improvement efforts.”

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