Pharma Technical Regulatory Submission Intern

Prepare global CMC regulatory submissions, including Module 3 CTD dossiers and electronic formatting standards, while managing regulatory information systems and documentation across diverse health authority types. Create and track project timelines to drive operational excellence and streamline workflows, applying data quality management practices using core business IT systems. Collaborate with cross-functional technical development teams to provide clear regulatory guidance and participate in agile methodologies like Scrum to support continuous improvement initiatives. This 12-month full-time internship begins January 2027 in Mississauga, ON, under a hybrid model requiring minimum three days in the office.