Principal Validation Engineer

  For CQV services in the Engineering  area.

WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree with eight (8) years of experience as a C&Q Engineer within the pharmaceutical or regulated industry.

Bilingual (English & Spanish).

Project Management skills.

Shift: Administrative, and according to business needs.

Experience in:  CQV Validation Expert: Risk-based qualification methods (ASTM E 2500) for pharmaceutical manufacturing equipment and utilities Sterilization & Cleaning Specialist (SME): CIP and SIP processes GMP Document Controller: Validation Protocols (IQ/OQ/PQ), Risk Assessments, and leading Root Cause Analysis (RCA) for quality issues.

Engineering Project Support: P&IDs and FAT/SAT.

The Personality Part:     Picture yourself in a lab… with all the equipment yo...

Ready to Apply?

Submit your application today and join our talented team at Flexible & Integrated Technical Services, LLC.