Pharmaceutical Regulatory Affairs & Quality Operations (RAQ)

Program overview

Focus your career by specializing in the Pharmaceutical Regulatory Affairs & Quality Operations program, a one-year graduate certificate offered by Seneca College. This program provides a fundamental understanding of regulatory affairs and quality operations, preparing you for a career in drug or medical regulations and quality assurance roles. You will study regulatory compliance both in Canada and internationally. The first semester covers the basics of regulatory affairs, while the second semester delves deeper into regulation and quality operations. An optional work term is available, allowing you to gain practical experience in your field.

Program structure

The Pharmaceutical Regulatory Affairs & Quality Operations program is structured to provide a comprehensive education over a duration of 2 semesters (1 year). Key features of the program include:

• Online and flexible delivery options, allowing students to choose between in-person and online learning.
• Optional work term(s) that provide hands-on experience in the field, similar in length to an academic semester.
• Part-time study options available for those who need flexibility.

This program is designed to equip students with the necessary skills and knowledge to excel in the pharmaceutical regulatory landscape, ensuring they are well-prepared for their future careers.

Featured Experiences

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

• Optional work term(s) that provide valuable hands-on experience in the industry.
• Interactive learning spaces for courses delivered in a flexible format, combining in-person and online instruction.
• In-class career workshops and one-on-one coaching to support students in securing work term positions.
• Exposure to real-world regulatory compliance scenarios through practical assignments and projects.

These experiences are designed to prepare students for the challenges of the pharmaceutical industry and to enhance their employability upon graduation.

Career Options

Graduates of the Pharmaceutical Regulatory Affairs & Quality Operations program can explore a variety of career options in Canada, including:

• Regulatory Affairs Associate: Responsible for ensuring that products meet regulatory standards and compliance requirements.
• Regulatory Affairs Assistant: Supports regulatory affairs teams in preparing documentation and submissions to regulatory bodies.
• Quality Assurance Associate: Monitors and ensures the quality of products and processes within the pharmaceutical industry.
• Quality Assurance Investigator: Conducts investigations into quality issues and ensures compliance with industry regulations.
• Documentation Administrator: Manages and maintains regulatory documentation and records for compliance purposes.
• Medical Information Associate: Provides information and support regarding medical products and regulatory requirements to healthcare professionals.

These roles are essential in maintaining the integrity and safety of pharmaceutical products, making graduates valuable assets in the industry.

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