Elevate your career with Zenith PV Solutions as a Senior Regulatory Affairs Specialist. This hybrid role focuses on Health Canada regulations and requires expertise in pharmacovigilance and client management.

As a seasoned professional in Regulatory Affairs, you will provide guidance and support for regulatory strategies and submissions. Your responsibilities include collaborating with executives, overseeing project timelines, and ensuring compliance with industry regulations. Leveraging your deep knowledge, you'll help strengthen Zenith's expanding client base and uphold high-quality service.

Key Responsibilities:
• Develop regulatory strategies for product submissions
• Handle NDSs and ANDSs for diverse pharmaceuticals




• Manage eCTD submissions efficiently for clients
• Participate in Health Canada pre-submission meetings
• Facilitate ongoing CMC filings and project onboarding

Requirements:
• MSc or equivalent in pharmaceutical sciences
• Minimum 5 years of RA experience in Canada
• Robust understanding of regulatory requirements
• Excellent English and French communication skills
• Robust project management abilities to meet deadlines

Bring your Regulatory Affairs expertise to Zenith PV Solutions and make an impact on client satisfaction.
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📌 Senior Regulatory Affairs Specialist in Toronto (Ontario)
🏢 Zenith PV
📍 Ontario