Regulatory Affairs Manager — Global Drug & Device Approvals

Novo Nordisk; Mississauga; On-site; CAD 100,000 - 120,000; Full time

Job summary

A leading pharmaceutical company in Mississauga is seeking a Regulatory Affairs Manager to ensure compliance and support drug approvals. The role requires a strong background in regulatory affairs, leadership skills, and experience in negotiation with regulatory agencies. Ideal candidates will have a B.Sc. degree and at least 5 years of relevant experience. This is an onsite position in a dynamic and engaging work environment.

Benefits

Opportunities for learning and development

Dynamic and inclusive work environment

Qualifications

• Minimum of 5 years of regulatory affairs experience, preferably in the pharmaceutical or biological industry.
• Experience in interacting with regulatory agencies and negotiating evidence.
• In-depth knowledge of advertising and promotional reviews.

Responsibilities

• Developing product registration applications, including supplements and clinical trials.
• Interacting and negotiating with regulatory agency personnel.
• Acting as a resource and mentor for colleagues.

Skills

Regulatory compliance

Leadership

Negotiation with regulatory agencies

Scientific background

Knowledge of Health Canada regulations

Education

B.Sc. in a relevant field

Job description

A leading pharmaceutical company in Mississauga is seeking a Regulatory Affairs Manager to ensure compliance and support drug approvals. The role requires a strong background in regulatory affairs, leadership skills, and experience in negotiation with regulatory agencies. Ideal candidates will have a B.Sc. degree and at least 5 years of relevant experience. This is an onsite position in a dynamic and engaging work environment.