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Engage in impactful regulatory activities as a Regulatory Affairs Associate III. Support clinical and labelling submissions, driving compliance in a hybrid work setting with three days onsite weekly.
This key role oversees daily regulatory clinical and labelling tasks for marketed and developing products. You'll compile and assess documentation for submissions to Health Canada while collaborating with local and global regulatory teams. Your expertise will also aid operational activities within the Regulatory Affairs department, ensuring effective communication with development and manufacturing groups.
Key Responsibilities:
• Provide regulatory support for major pharmaceutical submissions
• Manage filing of clinical and labelling changes




• Review promotional and non-promotional materials
• Update product labelling materials promptly
• Support launch activities for new products
Requirements:
• University degree in a science-related field
• Minimum 3 years in the pharmaceutical industry
• Working knowledge of Health Canada regulations
• Proficiency in Microsoft Office, especially Word and Excel
• Bilingual communication skills in French and English
Utilize your expertise to contribute significantly to regulatory success and support the introduction of creative products.
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Apply on Kit Job: kitjob.ca/job/2fs6da

📌 Regulatory Affairs Associate Hybrid Role (Toronto)
🏢 Teva Pharmaceuticals
📍 Toronto