Regulatory Affairs Manager at Teva (Toronto)

Lead regulatory strategy in Canada with Teva Pharmaceuticals as a Regulatory Affairs Manager in Scarborough, Ontario. Focus on submissions, product launches, and compliance within a hybrid work environment. Teva Pharmaceuticals is seeking a Regulatory Affairs Manager to spearhead Canadian regulatory planning for various medicinal products.

In this hybrid role, you will navigate the intricacies of Abbreviated New Drug Submissions, oversee labelling updates, and manage deficiency responses with precision. Collaborating with global teams, your expertise in health regulations will ensure timely product launches while adhering to evolving guidelines.

Key Responsibilities:

• Lead the preparation and submission of ANDSs and sANDSs
• Update product labelling materials for compliance
• Manage deficiencies and submission timelines
• Participate in essential regulatory meetings
• Act as Canadian regulatory lead in project teams

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Submit your application today and join our talented team at Teva Pharmaceuticals.

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