Senior Biopharmaceutical Downstream Process Specialist
4 weeks ago
Zoetis: A Leader in Animal Pharmaceuticals
Zoetis is a world-renowned manufacturer and supplier of animal pharmaceuticals. Our Lincoln, NE facility is a testament to our commitment to quality and excellence.
About the Role
We are seeking a highly skilled Biopharmaceutical Downstream Process Specialist to join our team. As a key member of our downstream process team, you will be responsible for supporting the design, qualification, operation, maintenance, and improvement of equipment and processes.
Key Responsibilities
- Apply advanced science and engineering principles to design and implement major system modifications, process, and/or capital projects.
- Support clinical and commercial tech transfers of late-stage Zoetis products from laboratories and across manufacturing facilities.
- Represent manufacturing and provide input to development teams.
- Develop, organize, analyze, and present interpretation of results for operational issues of significant scope and complexity.
- Conduct process monitoring and provide technical troubleshooting using sophisticated digital tools (PAT). Identify and implement process improvements that lead to yield and capacity improvements.
- Serve as a process expert of Biological and Biopharmaceutical operations and processes such as single-use technologies, Media/Buffer Prep solutions, Inoculation, Bioreactors, Centrifugation, Chromatography, and Tangential Flow Filtration.
- Author protocols, study reports, SOPs, and other documents in support of process changes/optimization.
- Mentor junior colleagues and provide direction to manufacturing colleagues and contractors.
- Provide technical guidance and lead investigations for process-related deviations, change control, and operational excellence projects.
- Demonstrate project management skills and application of concepts.
- Work within a cGMP environment and maintain regulatory and quality compliance.
Requirements
- Master's degree and 10 years of Downstream Process Development experience and tech transfer or scale-up experience.
- Or Bachelor's degree and 15 years of Downstream Process Development and tech transfer or scale-up experience.
- Master's or PhD degree in Biochemistry, Biology, or Biochemical Engineering.
- 10+ years Downstream Process Development experience related to biochemical engineering and/or protein biochemistry, scale-up principles, and manufacturing of Biopharmaceuticals (cGMP).
Benefits
- Great Health Benefits from day 1.
- 4 weeks accrued paid vacation and 13 paid holidays.
- 401(k) match with company profit sharing.
- Tuition reimbursement.
- Student Loan Repayment Program.
Work Environment
- 1st shift, 7:15am – 3:45pm.
- Travel to domestic and international sites may be required
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