Related engagement
Biologics CMC Analytical Dev. Consultant
Phase III biologics analytical development support with LCMS expertise and new CRO relationships.
Services
Engineering
Process engineering, validation, facilities qualification, and manufacturing readiness for regulated environments.
Overview
Engineering support at Viltis focuses on regulated manufacturing environments: CQV, facilities and utilities qualification, tech transfer, change control, process scale-up, GxP automation, and equipment reliability. The work is practical - protocols, execution, and records that stand up in audit.
Programs call when a new line is coming online, a transfer is at risk, deviations point to equipment or utility issues, or validation packages need to catch up with the floor. Our engineers work beside site teams so ownership stays with manufacturing and quality.
Open a capability below for detail, or talk with us about where engineering support would remove the most schedule risk. Viltis provides consulting and specialist resources; we do not certify equipment or facilities.
Engineering capabilities in this practice area include
- Commissioning, Qualification & Validation (CQV)
- Facilities & Equipment Qualification
- Manufacturing Readiness & Technical Transfer
- Engineering Change Control & Lifecycle Management
- Utilities & Cleanroom Systems Qualification
- Process Engineering & Scale-Up Support
- Automation & Control Systems (GxP)
- Equipment Reliability & Preventive Maintenance
Featured capabilities
Where teams typically start
Full directory
All Engineering capabilities
Need engineering support?
Discuss scope, timelines, and the specialists required for your program.