The role involves leading investigations for manufacturing deviations, events, and process issues within Windsor biologics operations
Job Summary
The role involves leading investigations for manufacturing deviations, events, and process issues within Windsor biologics operations.
Candidates will partner with Manufacturing, Quality, Engineering, QC, and MS&T to identify true root causes and implement corrective actions.
The position offers the opportunity to work with cutting-edge technologies at BIOVECTRA, a leader in contract development and manufacturing now part of Agilent.
Matching Summary
The role involves leading investigations for manufacturing deviations, events, and process issues within Windsor biologics operations.
Salary
Base: $27.59 - $48.29/hr CAD; Bonus/Equity: Eligible for bonus and stock; Benefits: Eligible for benefits
Skills & Requirements
Must-have
Bachelor's degree in Science or Engineering
GMP manufacturing experience in biologics
Root cause analysis (RCA) and investigation tools
CAPA development and effectiveness evaluation
Knowledge of Health Canada, FDA, and EMA standards
Nice-to-have
Strong technical writing skills
Experience with MasterControl or TrackWise QMS systems
Understanding of aseptic behavior and environmental monitoring
Ability to lead cross-functional teams
Proficiency in MS Office
Key Requirements
Bachelor's degree in Science, Engineering, Biotechnology, or related field
GMP manufacturing or quality experience preferably in biologics