Pharmaceutical Regulatory Affairs & Quality Operations (RAQ) (Seneca@York)

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 both Canadian and international regulatory compliance, preparing graduates for careers in drug and medical regulations as well as quality assurance roles. Students will gain a comprehensive understanding of the regulatory landscape and quality operations, ensuring they are well-prepared for the workforce. The program also offers an optional work term, allowing students to gain practical experience in their field of study.

Program structure

The Pharmaceutical Regulatory Affairs & Quality Operations program is structured to provide a thorough education over a duration of 2 semesters (1 year). The program includes:

• Fundamental studies in regulatory affairs and quality operations during the first semester.
• Advanced exposure to regulation and quality operations in the second semester.
• An optional work term, which is similar in length to an academic semester, providing hands-on experience.
• Flexible delivery options, including online and in-person classes.

This program is designed to accommodate both full-time and part-time students, ensuring that learners can tailor their education to fit their schedules. The work term option is available for students who meet the academic requirements, allowing them to gain valuable industry experience while studying.

Featured Experiences

The Pharmaceutical Regulatory Affairs & Quality Operations program offers several unique features that enhance the learning experience:

• Optional work term(s) that provide practical, hands-on experience in the field.
• Flexible delivery format, allowing students to choose between online learning and in-person classes.
• In-class career workshops and one-on-one coaching to prepare students for the work term.
• Interactive learning spaces that facilitate both online and in-person engagement.

These experiences are designed to ensure that students not only learn theoretical concepts but also apply them in real-world settings, making them more competitive in the job market.

Career Options

Graduates of the Pharmaceutical Regulatory Affairs & Quality Operations program can pursue a variety of 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 maintaining documentation.
• Quality Assurance Associate: Ensures that products meet quality standards and regulatory requirements.
• Quality Assurance Investigator: Conducts investigations into quality issues and ensures corrective actions are implemented.
• Documentation Administrator: Manages and organizes documentation related to regulatory submissions and quality processes.
• Medical Information Associate: Provides information and support regarding medical products and regulatory compliance.

These roles are critical in the pharmaceutical and healthcare sectors, ensuring that products are safe, effective, and compliant with regulations.

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