Join Teva Pharmaceuticals as a Regulatory Affairs Manager based in Scarborough, Ontario. Focus on regulatory leadership for generic medicines while working in a hybrid arrangement.
As the Regulatory Affairs Manager at Teva, you will lead the Canadian regulatory strategies for a variety of products, including complex generics and drug-device combinations. This hybrid role necessitates a deep understanding of Health Canada regulations, timely submissions, and collaboration across multidisciplinary teams to meet safety standards and product launches. Your strategic outlook will drive compliance and improvement within the regulatory function.
Key Responsibilities:
• Lead ANDS and sANDS submissions strategically
• Update product labeling and safety information
• Manage deficiencies and facilitate timely responses
• Participate in collaborative regulatory discussions
• Ensure compliance with local and global regulations
Requirements:
• Bachelor’s degree in a scienc...