Pharmaceutical Regulatory Affairs & Quality Operations (RAQ)

Program overview

The Pharmaceutical Regulatory Affairs & Quality Operations (RAQ) program is a one-year graduate certificate designed to equip students with essential knowledge in regulatory affairs and quality operations. This program focuses on understanding regulatory compliance both in Canada and internationally, preparing graduates for careers in drug and medical regulations as well as quality assurance roles. The curriculum is structured to provide a solid foundation in the first semester, followed by a more in-depth exploration of regulatory and quality operations in the second semester. An optional work term is available, allowing students to gain practical experience in their field.

Program structure

The Pharmaceutical Regulatory Affairs & Quality Operations program is structured as follows:

• Program Length: 2 Semesters (1 Year)
• Study Options: Full-time & Part-time
• Delivery: Online, Flexible
• Work Term Option: Available for students who meet academic requirements

This program is offered at the Seneca@York campus and online, with classes starting in January, May, and September. The flexible delivery format allows students to choose between in-person and online learning, enhancing their educational experience.

Featured Experiences

• Optional Work Term: Provides hands-on experience in the field, typically lasting the length of an academic semester.
• Flexible Delivery Format: Courses can be taken online or in-person, allowing for a personalized learning experience.
• Career Workshops: In-class workshops and one-on-one coaching to prepare students for the work term and job market.
• Prior Learning Assessment: Students can earn credit for previous studies or work experience.

Career Options

Graduates of the Pharmaceutical Regulatory Affairs & Quality Operations program can pursue various career paths in Canada, including:

• Regulatory Affairs Associate: Responsible for ensuring compliance with regulations and guidelines in the pharmaceutical industry.
• Regulatory Affairs Assistant: Supports regulatory affairs teams in preparing submissions and documentation for regulatory bodies.
• Quality Assurance Associate: Ensures that products meet quality standards and regulatory requirements throughout the production process.
• Quality Assurance Investigator: Conducts investigations into quality issues and ensures corrective actions are implemented.
• Documentation Administrator: Manages and maintains regulatory documentation and records for compliance purposes.
• Medical Information Associate: Provides information and support regarding pharmaceutical products to healthcare professionals and patients.

DISCLAIMER: The information above is subject to change. For the latest updates, please contact LOA Portal's advisors.