Biopharmaceutical Downstream Process Specialist

1 week ago


Lincoln, Lincolnshire, United Kingdom Zoetis Full time

Company Overview


Zoetis is the world's largest manufacturer and supplier of animal pharmaceuticals, serving customers by providing high-quality medicines for dogs, cats, and livestock.


Estimated Salary: $120,000 - $180,000 per year


Job Description


We are seeking a skilled Biopharmaceutical Downstream Process Specialist to join our team in Lincoln, NE. As a key member of our manufacturing team, you will be responsible for supporting robust processes and innovative technologies using scientific and engineering expertise.


The role involves providing technical support for complex equipment and biological and biopharmaceutical processes. You will be required to design, qualify, operate, maintain, and improve equipment and processes to support day-to-day manufacturing activities and lead process improvement projects and technical transfers.


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 results for operational issues of significant scope and complexity.
  • Conduct process monitoring and provide technical troubleshooting using sophisticated digital tools (PAT).
  • 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.

Requirements



  • Master's degree or equivalent in Biochemistry, Biology, or Biochemical Engineering, or related field.
  • 10+ years of downstream process development experience related to biochemical engineering and/or protein biochemistry, scale-up principles, and manufacturing of biopharmaceuticals (cGMP).
  • Strong academic and applied experience in science and/or engineering, troubleshooting, and problem-solving.
  • Demonstrated leadership skills and decision-making experience.
  • Excellent written and verbal communication with experience in technical writing and presentations.
  • Process optimization and change control experience.

Benefits



  • Great health benefits from day one.
  • Four weeks accrued paid vacation and 13 paid holidays.
  • 401(k) match with company profit sharing.
  • Tuition reimbursement.
  • Student loan repayment program.


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