Expand GSK's regulatory frontiers with your expertise as a Regulatory Affairs Manager. This hybrid position centers on achieving swift product approvals and compliance management.
GSK is looking for an experienced Regulatory Affairs Manager specializing in CMC and Oncology to lead regulatory submissions. The role demands deep familiarity with Canadian regulations and the ability to build effective relationships with Health Canada. You will play a crucial role in preparing and filing submissions timely while ensuring all compliance needs align with business objectives.
Key Responsibilities:
• Develop and implement regulatory strategies for product approvals
• Manage regulatory submissions and compliance for various products
• Foster relationships with Health Canada to expedite approvals
• Ensure alignment with GSK and industry regulatory guidelines
• Mentor junior staff and contribute to their regulatory knowledge
Requirements:
• Bachelor’s degree in life sciences or related field
• Significant experience in Canadian regulatory affairs
• Solid understanding of Canadian regulatory guidelines
• Exceptional communication and influencing skills
• Project management experience is essential
Bring your regulatory insight and strategic thinking to contribute to GSK's mission in Canada.
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