Process Engineer-Production Systems, Oral Solid Dose
Job in
Bridgeton, St. Louis city, Missouri, 63044, USA
Listed on 2026-05-31
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
Job Description & How to Apply Below
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.
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.
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.
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.
Support Production Training
- Develop general training material related to process engineering.
- Serve as Subject Matter Expert and trainer for process engineering knowledge.
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.
- 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.
- 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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