Process Engineer

3 weeks ago


Elizabeth, New Jersey, United States Zoetis Full time

Job Summary

Zoetis is seeking a highly skilled Process Engineer to join our team. As a Process Engineer, you will be responsible for providing biochemical process engineering support for formulation, testing, and reagent beads. You will use industry best practices and your expertise in biochemistry to measure, analyze, and specify requirements that lead to best-in-class quality products and design for manufacturability.

Key Responsibilities

  • Improve testing methods and quality control measures for reagents, incoming materials, standards, and controls.
  • Perform reagent and finished product testing as needed. Utilize common analytical methods such as UV-Vis, FTIR, DSC, TGA, MFI, stress strain, SEM, etc.
  • Build test finished products as necessary as part of root-cause investigation.
  • Investigate root cause of production issues impacting product quality or yield, support implementation of improvement and countermeasures.
  • Identify sources of variation (procedure, process, equipment, people) within the manufacturing process and design solutions.
  • Recognize need for and embrace concept of continuous improvement. Create new ideas and recommendations based on engineering data, facts, and observations.
  • Collect process data, perform trending, and statistical evaluation to monitor process performance to understand stability and areas for improvement.
  • Effectively partner with and motivate enabling support teams to improve operations for the advancement of the whole site and company.
  • Maintain quality control and safety standards.
  • Actively contribute to meeting business objectives around compliance, cost savings, and potentially capital spend requirements.
  • Assist in completing validation activities as required.
  • Assist in non-conformance and CAPA investigations.
  • Update procedures as necessary.

Requirements

  • BS/MS in Chemistry, Chemical Engineering, Material Engineering, and/or Biology with 2+ years of experience in a manufacturing environment.
  • Food and Drug Administration, USDA, and/or Drug Product Formulation is required.
  • Experience with lyophilization and test methods validation is preferred.
  • Demonstrated ability to interact effectively with colleagues and management across departmental boundaries.
  • Candidate must possess flexibility and agility to respond to constantly changing conditions and priorities.
  • Proficient computer skills such as Excel, Word, MS Visio, JMP, Minitab, or similar software.
  • Must be willing to quickly learn and become proficient in common systems used to manage the business – to include production schedule, quality deviations, ERP system, and change control.
  • Work Environment: Colleague must work onsite, be able to lift at least 50 pounds, and work near moving mechanical parts with moderate noise level where the use of hearing protection is optional and eye protection is required.

Benefits

This position is eligible for short-term incentive compensation. We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, and retirement savings benefits along with paid holidays, vacation, and disability insurance.


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