Poultry Process Improvement Lead

Zoetis, Inc

Charles City (IA)

On-site

USD 90,000 - 130,000

Full time

5 days ago
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Job summary

Zoetis, Inc. in Charles City, IA is seeking a Manufacturing Lead to drive the introduction of new methods and processes, partnering with GMT and QA to improve efficiency, yield and regulatory compliance.

The role requires strong technical/analytical skills, cross-functional collaboration, and hands-on process optimization in a biologics manufacturing setting. You will lead investigations, implement corrective actions, work with suppliers, and train colleagues on best practices to maintain cGMP

Qualifications

  • Bachelor's Degree in Poultry Science or related technical field.
  • Strong technical/analytical skills and ability to interact across divisional boundaries.
  • Working knowledge of GLP or cGMP and regulatory guidelines (FDA, USDA, APHIS).
  • Lean/Six Sigma experience; Green Belt preferred or commitment to certification within 1 year.

Responsibilities

  • Take the manufacturing lead in introducing new methods or modifications to processes.
  • Collaborate with GMT, Manufacturing Team, QA, Regulatory and Engineering as needed.
  • Work with suppliers and Procurement to ensure proper materials are used.
  • Lead process improvement initiatives to reduce bioburden, contamination and increase yield.
  • Author investigations and corrective actions using RFT tools and scientific reasoning.
  • Train colleagues on best practices and ensure compliance with GMP requirements.

Skills

Technical/analytical skills
Interpersonal skills
Cross-functional collaboration
GMP/cGMP knowledge
Lean/Six Sigma
Technical writing
Regulatory awareness

Education

Bachelor's Degree in Poultry Science
MBA/MS in a relevant field
Minimum 8 years relevant experience

Job description

Zoetis, Inc. in Charles City, IA is seeking a Manufacturing Lead to drive the introduction of new methods and processes, partnering with GMT and QA to improve efficiency, yield and regulatory compliance.

The role requires strong technical/analytical skills, cross-functional collaboration, and hands-on process optimization in a biologics manufacturing setting. You will lead investigations, implement corrective actions, work with suppliers, and train colleagues on best practices to maintain cGMP

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