Job Description
This position is responsible for ensuring quality systems work properly and in compliance with Positive Manufacturing Practices and Health Canada Guidelines.
This position is responsible for monitoring GMP-related activities for the company such as Product Releases, Deviation Management, Change Control Management, CAPA Management, Master document Management, SOP Management, Annual Confirmatory Testing program, and 3pl warehouse activities, etc.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day.
We are an equal opportunity/affirmative action employer that believes everyone matters.
Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances.
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[email protected].
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Skills and Requirements
· Minimum University level degree (B.
Sc.) in a Science or Pharmacy discipline applicable to Health Canada Standards
· Minimum 3+ years of experience in the pharmaceutical industry, specifically in Quality Assurance/ Quality Control department working under Health Canada GMP regulations
· Excellent communication skills, both written and verbal
· Knowledge of Health Canada Guidelines will be preferred
· Knowledge of GMP and regulatory requirements for the pharmaceutical industry.
Strong proficiency with applicable computer software and MS applications.
📌 QA Associate (Concord)
🏢 Insight Global
📍 Concord