Regulatory Affairs Associate, Post-Approval

KEY RESPONSIBILITIES

• Prepares generic drug product submissions for Health Canada (eg NCs, SANDSs, DINAs, etc). Ensures that submissions are accurate and meet format and content requirements.
• Reviews, evaluates, prepares, and files deficiency responses to Health Canada in a timely manner within given deadlines.
• Evaluates change requests.
• Reviews and contributes to implementation of post-approval changes of drug products.
• Interprets scientific data and conclusions from CMC reports and summaries.
• Attends, and may organize and facilitate, meetings and teleconferences with external partners and internal stakeholders to maintain progress of projects. Tracks and communicates critical attributes of projects to ensure accountability and efficiency.
• Maintains a healthy working relationship with business partners. Liaises with partners to collect documents and information for submission preparation or in response to technical queries / deficiency letters from Regulatory Agencies.
• Contributes to an efficient and effective regulatory affairs team, and uses knowledge and expertise towards a culture of continuous improvement.
• Maintains current awareness of regulatory guidelines (Health Canada, ICH, FDA, etc) and shares knowledge with the department.

TECHNICAL SKILLS :

LEADERSHIP SKILLS :

QUALIFICATIONS :

Skills Required

Regulatory Compliance, Document Review, Risk Assessment, Quality Assurance, Clinical Trials