Regulatory Affairs Associate – Injectable Submissions

A pharmaceutical company in Oakville, Ontario, is seeking an Associate in Regulatory Affairs to prepare regulatory submissions for complex injectable products. The ideal candidate will have at least 3 years of experience with drug submissions in Canada, particularly for parenteral dosage forms. Responsibilities include coordinating submission documentation, ensuring regulatory compliance, and handling lifecycle management activities. Knowledge of Health Canada regulations is essential.

This position offers the chance to contribute to a dedicated regulatory affairs team.
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