Site Quality Events Lead

Agilent Technologies UK

Windsor, Nova Scotia, Canada
Base: $31.92 - $55.86ph cad; bonus/equity: eligibl...
Bachelor's degree in science or engineering
6+ years gmp manufacturing experience
Expertise in rca and capa effectiveness
The role leads the site investigation program for manufacturing, environmental, contamination, and process-related events at BIOVECTRA, now part of Agilent Technologies

Job Summary

  • The role leads the site investigation program for manufacturing, environmental, contamination, and process-related events at BIOVECTRA, now part of Agilent Technologies.
  • Candidates will ensure timely, compliant, and scientifically sound investigations while driving the effectiveness of Corrective and Preventive Actions (CAPAs).
  • This position offers the opportunity to work with cutting-edge technologies in microbial fermentation, synthetic small molecules, and sterile filling capabilities.

Matching Summary

The role leads the site investigation program for manufacturing, environmental, contamination, and process-related events at BIOVECTRA, now part of Agilent Technologies.

Salary

Base: $31.92 - $55.86/hr CAD; Bonus/Equity: Eligible for bonus and stock; Benefits: Eligible for benefits

Skills & Requirements

Must-have

  • Bachelor's degree in Science or Engineering
  • 6+ years GMP manufacturing experience
  • Expertise in RCA and CAPA effectiveness
  • Knowledge of CGMP, ICH, and Health Canada standards
  • Experience leading cross-functional investigation teams

Nice-to-have

  • Advanced degree in applicable field
  • Experience supporting FDA, EMA, or Health Canada inspections
  • Knowledge of biologics upstream/downstream operations
  • Strong technical writing and presentation skills
  • Familiarity with contamination control strategies

Key Requirements

  • Bachelor's degree in Science or Engineering required
  • Minimum 6 years of GMP manufacturing environment experience
  • Proven expertise in Root Cause Analysis (RCA) and CAPA management
  • Experience representing sites during regulatory audits (FDA, Health Canada)

Work Rights

Not specified

Tailored Resume

Cover Letter