Global Pharma Regulatory Submissions Intern

F. Hoffmann-La Roche AG; Mississauga; Hybrid; CAD 57,000 - 75,000; Full time

Job summary

Roche is seeking a Pharma Technical Regulatory Submission Intern in Mississauga for a 12-month hybrid internship. You will support high-quality regulatory submissions, manage information systems, and help streamline workflows within a global regulatory team.

This role builds core expertise in regulatory operations, project management, and data systems while contributing to patient outcomes. Ideal candidates are enrolled in a Master’s degree in biotechnology or related field, with a completed

Qualifications

• Knowledgeable in pharmaceutical/biotechnology industry operations and drug development processes.
• Highly detail-oriented with proven abilities in data consistency, proofreading, and language mechanics.
• Tech-savvy and adaptable, with a strong drive to leverage digital tools for efficient workflows.
• Organized team player and strong communicator who thrives under pressure and dynamic priorities.

Responsibilities

• Prepare global (CMC) regulatory submissions, including Module 3 CTD dossiers and electronic formatting standards.
• Manage regulatory information systems and documentation across diverse health authority submission types.
• Create and track project timelines to drive operational excellence and streamline regulatory workflows.
• Apply data quality management practices using core business IT systems to support data-driven content management.
• Collaborate with cross-functional technical development teams to provide clear regulatory guidance.
• Participate in agile methodologies (such as Scrum) to support continuous improvement initiatives.

Education

Master’s degree in Biotechnology or related field

Bachelor’s degree in life sciences

Job description

Roche is seeking a Pharma Technical Regulatory Submission Intern in Mississauga for a 12-month hybrid internship. You will support high-quality regulatory submissions, manage information systems, and help streamline workflows within a global regulatory team.

This role builds core expertise in regulatory operations, project management, and data systems while contributing to patient outcomes. Ideal candidates are enrolled in a Master’s degree in biotechnology or related field, with a completed