Regulatory Affairs Associate Salary in Montréal, Québec

Regulatory Affairs Associate job description

Job Title: Regulatory Affairs Associate

Overview/Summary of the role:

A Regulatory Affairs Associate is responsible for monitoring and ensuring compliance with regulatory requirements and guidelines set forth by governmental agencies that govern the development, production, and marketing of pharmaceutical, biotechnology, or medical device products. The role is crucial in ensuring that products are safe for consumer use and are approved by regulatory agencies before they are released.

Responsibilities and Duties:

- Prepare and submit regulatory submissions to regulatory agencies such as FDA, EMA, and other regional regulatory authorities

- Monitor regulatory guidelines and notify departments of changes in regulations and guidelines that may affect their activities

- Coordinate and track regulatory documentation activities to ensure timely submission

- Review and approve labeling, advertising, and promotional materials for regulatory compliance

Regulatory Affairs Associate interview questions

Interviewer: Good morning/afternoon, please introduce yourself and explain how your experience aligns with this Regulatory Affairs Associate position?

Candidate: Good morning/afternoon, my name is John Doe. I have a Bachelor's degree in Biochemistry, and I have worked as an intern in the regulatory affairs department at XYZ Pharmaceuticals for three years. During that time, I have gained experience in preparing and submitting regulatory documents, tracking regulatory changes, and managing the database for the department.

Interviewer: Can you explain your understanding of Regulatory Affairs?

Candidate: Regulatory Affairs is the process of ensuring that a medical product meets regulatory requirements and standards set by governing bodies such as the FDA. It involves compiling and submitting documentation to demonstrate the safety and efficacy of the product as well as ensuring compliance with regulations.

Interviewer: Can you explain your experience working with regulatory submissions?

Candidate: As an intern at XYZ Pharmaceuticals, I have worked on regulatory submissions for new drug applications (NDA), abbreviated new drug applications (ANDA), and investigational new drug applications (INDA). I have experience in compiling and submitting regulatory documents, maintaining and tracking documents, and eCTD submissions.