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Process Engineer-Production Systems, Oral Solid Dose

Job in Bridgeton, St. Louis city, Missouri, 63044, USA
Listing for: Virbac Corporation
Full Time position
Listed on 2026-05-31
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Quality Engineering, Chemical Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Bridgeton

Overview

Virbac Animal Health is seeking a Process Engineer for our Industrial Operations teams. The role focuses on oral solid dose (granulation, compression) process optimization and supports new product launches through engineering expertise.

Responsibilities Area of responsibility 1:
Technical Resource for Manufacturing Processes
  • Standardize existing manufacturing processes (equipment and steps) to increase robustness and compliance.
  • Develop and implement process improvements in collaboration with the Industrial Operations Team.
  • Troubleshoot and resolve manufacturing process problems, performing investigations and determining root causes and corrective actions.
  • Monitor and improve the efficiency, output, and safety of manufacturing processes through observation, measurement, and data analysis.
  • Support the Corporate Risk Management program.
Area of responsibility 2:
Process Engineering Documentation
  • Develop process documentation and training material to support standardized processes and new product launches.
  • Provide documentation to support compliance requirements for existing products and new product regulatory filings.
Area of responsibility 3:
Collaboration in New Product Development
  • Provide process engineering recommendations to R&D and MSAT during development phases to ensure robust manufacturability.
  • Advise on compliance and product quality during the development phase.
Area of responsibility 4:
Collaboration in New Product Launches
  • Participate in technology transfer to transition new products into production.
  • Ensure new processes meet production, quality, and compliance requirements.
  • Provide guidance on manufacturing equipment and systems purchases.
Area of responsibility 5:
Support Production Training
  • Develop general training material related to process engineering.
  • Serve as Subject Matter Expert and trainer for process engineering knowledge.
Area of responsibility 6:
Support Continuous Improvement Activities
  • Participate in kaizen events and develop new support systems, incorporating a quality perspective.
  • Identify and lead continuous improvement initiatives to eliminate waste and increase efficiency.
  • Review process history to identify improvement trends.
Qualifications
  • 5-7 years of increasing responsibility in a pharmaceutical cGMP environment.
  • BS in Chemical or Mechanical Engineering (preferred).
  • Prior proven experience processing powders (oral solid dose, granulation, compression).
  • Experience with extrusion processes (preferred).
  • Leadership experience of process improvement teams.
  • Experience in pharmaceutical or other FDA‑regulated industry.
  • Experience applying lean and Six Sigma principles and tools (preferred).
  • Ability to travel up to 10% of the time.
Compensation & Benefits
  • Competitive base compensation and bonus opportunities.
  • 401(k) match: 6%.
  • Paid time off (prorated): 13 days.
  • Company‑paid holidays: 15.
  • Vacation days: 5.
  • Personal days: 5.
  • Floating holidays: 5.
  • Growth opportunities through professional development and internal mobility.
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