Become a key player in drug product registration as a Senior Associate in Regulatory Affairs. Ensure compliance, manage submissions, and collaborate with diverse teams to impact health positively. This full-time position in Toronto requires a minimum of four years of experience in Regulatory Affairs.
You will manage the preparation of important submissions, engage with Health Canada, and provide regulatory guidance to internal teams. Your role is crucial in aligning regulatory strategies with business goals while addressing emerging issues and improving department processes.
Key Responsibilities : • Oversee regulatory strategic plans for product registrations • Manage New Drug Submission and lifecycle maintenance • Collaborate with Health Canada for submission reviews • Work with cross-functional teams on regulatory strategies • Provide guidance on promotional material and messaging
Requirements : • B.Sc. in Biological sciences; MSc/PhD preferred • 4+ years of regulatory experience required • Knowledge of Canadian drug development essential • Strong problem-solving and writing abilities needed • Ability to interpret clinical data and biostatistics Be part of a transformative healthcare journey, enhancing lives through effective regulatory strategies and submissions.
Monday to Friday, 9 AM – 5 PM (full-time)
Submit your application directly to Johnson & Johnson.
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