Senior Scientist, Biopharma Pilot GMP Scale-Up

Zoetis, Inc

Lincoln (NE)

On-site

USD 90,000 - 130,000

Full time

14 days+
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Job summary

Zoetis, Inc. in Lincoln, Nebraska seeks a Senior Associate Scientist for the Biopharmaceutical Pilot Registration Lab to lead development, scale-up and tech transfer of CHO-expressed mAbs for veterinary use.

The role requires hands-on GMP experience in upstream and/or downstream processing and strong collaboration with global teams. The position emphasizes process documentation, cross-functional leadership, and readiness to support programs from development through pilot to commercial

Qualifications

  • Bachelor's degree in biological sciences or related field required; advanced degree helpful.
  • Experience in upstream cell culture and/or downstream processing in GMP environments.
  • Proven track record with tech transfer and scale-up-to-commercial facilities.

Responsibilities

  • Advanced experience in setting up, programming, operating and troubleshooting large-scale equipment for expression and/or purification.
  • Represent the lab as a technical leader, driving process optimization and scale-up and tech transfer.
  • Author and review process documents, SOPs, protocols and regulatory filings with scientific rigor.
  • Hands-on support of upstream cell culture (shake flask to 2000-L) and/or downstream purification.
  • Drive continuous improvement and optimize workflows; maintain compliant documentation.
  • Perform preventative maintenance on portable and stationary equipment; execute steam-in-place procedures.

Skills

Advanced process scale-up experience
Troubleshooting large-scale equipment
Cross-functional leadership
Aseptic technique
Strong written and verbalcommunication

Education

Bachelor's degree in biological sciences or related field
Advanced degree advantageous

Tools

SCADA
DeltaV
Unicorn
GMP SAP / LIMS
Centrifugation equipment
Chromatography systems
Filtration systems

Job description

Zoetis, Inc. in Lincoln, Nebraska seeks a Senior Associate Scientist for the Biopharmaceutical Pilot Registration Lab to lead development, scale-up and tech transfer of CHO-expressed mAbs for veterinary use.

The role requires hands-on GMP experience in upstream and/or downstream processing and strong collaboration with global teams. The position emphasizes process documentation, cross-functional leadership, and readiness to support programs from development through pilot to commercial

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