Regulatory Affairs Operations Excellence Associate (12 Month Contract)

AstraZeneca

Toronto, Canada
Base: 75,752.00 - 99,424.50; bonus/equity: annual ...
Health canada correspondence processing
Global regulatory information management system data entry
Submission document coordination
Your role will be crucial in supporting the timely and high-quality preparation and delivery of Canadian submissions and optimization of product labelling in accordance with AstraZeneca standards and our local GxP Quality Management System (QMS)

Job Summary

  • Your role will be crucial in supporting the timely and high-quality preparation and delivery of Canadian submissions and optimization of product labelling in accordance with AstraZeneca standards and our local GxP Quality Management System (QMS).
  • You will play an active role in enhancing team efficiency, performance, and productivity, while ensuring compliance with AstraZeneca's corporate responsibility policies.
  • AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination.

Matching Summary

Your role will be crucial in supporting the timely and high-quality preparation and delivery of Canadian submissions and optimization of product labelling in accordance with AstraZeneca standards and our local GxP Quality Management System (QMS).

Salary

Base: 75,752.00 - 99,424.50; Bonus/Equity: Annual Variable Pay Bonus/Short Term Incentive opportunity; Benefits: Contract Benefits Program

Skills & Requirements

Must-have

  • Health Canada correspondence processing
  • Global Regulatory Information Management System data entry
  • submission document coordination
  • product labelling QC reviews
  • GxP Compliance and QMS activities

Nice-to-have

  • collaborative culture
  • ambitious thinking and innovation
  • individualized flexibility
  • dedication to sustainability
  • customer-focused approach

Key Requirements

  • University degree in health science or equivalent experience
  • 1-2 years pharmaceutical/biotech experience
  • Knowledge of Canadian regulatory environment
  • Familiarity with electronic labeling systems
  • Proficient in MS Office and document management systems

Work Rights

Not specified

Tailored Resume

Cover Letter