Senior Biopharma Pilot & Tech-Transfer Scientist

Zoetis

Lincoln (NE)

On-site

USD 95,000 - 135,000

Full time

44 hours ago
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Job summary

Zoetis in Lincoln, Nebraska, is seeking a Senior Associate Scientist to support development, scale-up and tech transfer of CHO-expressed monoclonal antibodies for veterinary use within a GMP environment.

You will collaborate with multidisciplinary teams to ensure smooth transitions from development to pilot to commercial manufacturing, with hands-on work in upstream/downstream processing and strong documentation practices.

Qualifications

  • Bachelor-level degree in biological sciences, chemical engineering, or related field.
  • Experience with upstream cell culture and/or downstream processing in GMP settings.
  • Proven GMP track record including process scale-up and tech transfer.

Responsibilities

  • Set up and troubleshoot large-scale expression and purification equipment.
  • Lead cross-functional teams in process transfer and scale-up.
  • Author and review process docs, SOPs, and tech transfer filings.
  • Support upstream cell culture from shake flask to 2000-L scales.
  • Drive workflow improvements and maintain GMP-compliant docs.
  • Perform preventative maintenance on lab equipment.
  • Maintain steam-in-place procedures and equipment cleaning.
  • Ensure regulatory compliance and accurate record-keeping.

Skills

Cell culture
Downstream processing
Tech transfer
GMP compliance
SOP documentation
Data capture systems

Education

Biological sciences degree
Chemical/biochemical engineering degree
Advanced degree preferred

Tools

SCADA
DeltaV
Unicorn
LIMS
SAP

Job description

Zoetis in Lincoln, Nebraska, is seeking a Senior Associate Scientist to support development, scale-up and tech transfer of CHO-expressed monoclonal antibodies for veterinary use within a GMP environment.

You will collaborate with multidisciplinary teams to ensure smooth transitions from development to pilot to commercial manufacturing, with hands-on work in upstream/downstream processing and strong documentation practices.

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