Scientist / Sr. Scientist - Biopharm Pilot Registration Lab

Zoetis

Lincoln (NE)

On-site

USD 80,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Competitive healthcare benefits
Retirement savings benefits
Employee wellness programs

Job summary

A leading veterinary health company in Lincoln, NE, is seeking a Scientist / Sr. Scientist for their Biopharm Pilot Registration Lab. This role involves developing and scaling processes for monoclonal antibodies in a GMP environment. Candidates should possess significant expertise in downstream processing and experience in GMP-regulated settings. The role offers competitive benefits and a focus on employee well-being.

Qualifications

  • Advanced experience with large-scale equipment for purification of recombinant proteins.
  • Proven track record in GMP-regulated environments including tech transfer.
  • Excellent written and verbal communication skills.

Responsibilities

  • Operate and troubleshoot large-scale equipment for protein purification.
  • Execute GMP batches for downstream purification processes.
  • Represent the lab in cross-functional project teams.

Skills

Downstream processing expertise
Strong organizational skills
Excellent communication skills
Aseptic technique
Proven ability to work independently

Education

Advanced degree in biological sciences or chemical engineering
BS and 7+ years or MS and 6+ years of experience for Scientist
MS and 15+ years or PhD and 1-2 years of experience for Sr. Scientist

Tools

GMP systems (change control, SAP, LIMS)
Instrumentation and control systems
Single-use bioreactor technology

Job description

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As a Scientist in the Biopharmaceutical Pilot Registration Lab, you will play a vital role in the development, scale-up, and technology transfer of CHO-expressed monoclonal antibodies for veterinary use. You will operate in a GMP-regulated environment, collaborating with multidisciplinary teams to ensure a successful transition from development to pilot to commercial manufacturing. This role requires hands-on technical expertise in downstream processing, as well as strong organizational and communication skills. The position is based in Lincoln (Nebraska, USA) with frequent interactions with colleagues and external partners located around the globe.

Position Responsibilities

  • Advanced experience in setting up, programming, operating and troubleshooting large-scale equipment for purification of recombinant therapeutic proteins
  • Execute GMP batches for downstream purification (centrifugation, chromatography, precipitation, ultrafiltration, sterile filtration)
  • Support upstream operations (aseptic inoculation, cell culture growth at 50L-2000L scale)
  • Perform preventative maintenance on portable and stationary equipment
  • Maintain, clean, and perform steam-in-place procedures for equipment
  • Demonstrate advanced expertise in authoring and reviewing process documentation, SOPs, protocols, technology transfer documents and regulatory filings ensuring the highest standards of scientific rigor and quality
  • Ensure accurate and compliant record-keeping in accordance with current GMP standards
  • Represent the lab as a key technical leader in cross-functional project teams, collaborating with process development and manufacturing teams, driving process optimization and scale-up, ensuring seamless, high-quality technology transfer
  • Drive continuous improvement by optimizing existing workflows and procedures

Education and Experience

  • Advanced degree in biological sciences, chemical engineering, or related field is preferred
  • For Scientist: BS and 7+ years of experience or MS and 6+ years of experience
  • For Sr. Scientist: MS and 15+ years of experience or PhD and 1-2 years of experience
  • Significant practical experience and theoretical knowledge of downstream processing (centrifugation, filtration, chromatography) and upstream cell culture.
  • Proven track record in GMP-regulated environments, including process scale-up and tech transfer to commercial facilities.

Technical Skills Requirements

  • Strong scientific and engineering background in the principles for process scale-up and robustness
  • Experience with instrumentation, control systems, and advanced troubleshooting for pilot-scale GMP operations, including practical experience with automated control and data capture systems such as SCADA, Delta V, and Unicorn
  • Knowledge of equipment specification, qualification, operation, and maintenance in a regulated environment
  • Experience with large-scale single-use bioreactor technology and mammalian cell culture is desirable.
  • Working knowledge of GMP systems (change control, SAP, LIMS) is desirable
  • Willingness to work flexible hours, including after-hours monitoring as needed
  • Ability to perform physically demanding tasks typical of a pilot-scale lab environment
  • Excellent aseptic technique
  • Experience with cGMPs, inspection, and compliance in a pilot lab setting
  • Demonstrated ability to work independently on multiple concurrent programs
  • Familiarity with regulatory frameworks for veterinary biopharmaceuticals is desirable
  • Strong organizational and people skills
  • Excellent written and verbal communication skills
  • Proven ability to work effectively as part of a collaborative team

About Zoetis

At
Zoetis, our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues' careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources.

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Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Research and Science
  • Industries
    Research Services and Veterinary Services

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