Senior Biopharmaceutical Downstream Process Specialist

4 weeks ago


Lincoln, Lincolnshire, United Kingdom Zoetis Full time

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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