Lead Regulatory Affairs at Teva

Take charge of regulatory affairs with Teva Pharmaceuticals as a Regulatory Affairs Manager in Scarborough, Ontario. This hybrid role emphasizes compliance, submissions, and product launch strategies in the pharmaceutical sector.

As a regulatory lead, you will handle Abbreviated New Drug Submissions and update product labelling for compliance. You'll collaborate with global teams to uphold health regulations and support timely launches of medicinal products.

Key Responsibilities:

• Prepare and submit ANDSs and sANDSs

• Ensure product labelling meets compliance standards

• Manage deficiencies and maintain submission timelines

• Engage in essential regulatory meetings

• Lead Canadian regulatory efforts in project teams

Requirements:

• Bachelor’s degree in a science-related field

• At least 5 years in the pharmaceutical industry

• Solid regulatory strategy experience

• Knowledge of complex generics and biosimilars

• Familiarity with Health Canada regulations

Leverage your leadership in regulatory affairs at Teva Pharmaceuticals to drive compliance and successful launches.
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