Senior Associate – Regulatory Affairs at J&J

Take on a key role as a Senior Associate in Regulatory Affairs at Johnson & Johnson in Toronto, Ontario. This 12-month contract is centered on regulatory compliance and product lifecycle management.

As a senior associate, you will act as a subject matter expert, guiding regulatory strategies for drug products. Your responsibilities will include preparing regulatory submissions and collaborating with Health Canada to ensure compliance with regulations. Engage with cross-functional teams to support business goals and enhance processes within the department.

Key Responsibilities:

• Develop strategic plans for regulatory submissions

• Oversee New Drug and Supplemental New Drug submissions

• Respond to regulatory queries from Health Canada

• Foster partnerships with internal and external stakeholders

• Address emerging regulatory issues proactively

Requirements:

•

B.Sc. in Biological Sciences minimum, MSc/PhD preferred

• 4 years of experience in pharmaceutical Regulatory Affairs

• Understanding of Canadian regulations and drug development

• Strong problem-solving and analytical skills

• Communication skills for effective collaboration

Advance your career in Regulatory Affairs with Johnson & Johnson and influence drug registration processes in Toronto.
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