Develops regulatory strategies for rapid approvals with optimal labelling for products within therapy or for submissions within specialization area.
Accountable for a portfolio of products, including the preparation, filing and approval of regulatory submissions (NDSs, SNDSs, CTAs, NCs, etc) to aggressive targets.
Ensures compliance with applicable Health Canada, industry, and GSK codes and guidelines in alignment with business needs.
Builds trust with Health Canada contacts to improve GSK submission approval times, achieve competitive labelling and resolve product related issues impacting submissions, supply continuity, or compliance activities.
Communicates with and influences multiple local and global functions to achieve regulatory objectives.
Identifies and responds to issues related to assigned projects and/or products.
Interprets Canadian regulations, guidelines and policies as they apply to GSK regulatory activities.
Mentors junior staff.
Qualifications Required:
B.Sc. in life science or relevant scientific field (e.g. pharmacology, toxicology, chemistry)
Extensive Canadian regulatory affairs experience leading multiple submissions at all stages of the product lifecycle
Must possess a thorough understanding of the Canadian Food & Drug Regulations, relevant guidelines and policies
Must possess a thorough understanding of drug development and commercialization process
Highly innovative (strategic and functional) and creative problem solver and decision maker who can apply continuous improvement techniques to gain efficiencies in submission preparation, product approval process, and resolving issues
Agile and able to effectively navigate change
Demonstrated ability to develop effective regulatory strategies aligned with commercial objectives
Working knowledge of global regulatory agencies and their practices
Excellent oral and written communication skills including the ability to present information and contribute ideas in small and large groups
Good influencing and relationship management skills
Excellent negotiation skills
Fully developed project management skills
Must act with integrity and demonstrate a strong and effective risk management perspective
Ability to provide and receive feedback, raise issues, share experiences and lessons learned
Proactive and seeks to constantly learn and develop, ensures that skills meet changing business needs
Fosters strong team collaboration, with the ability to engage constructively with others and demonstrate a positive mindset. Open to diverse ideas, styles and perspectives
Strong commitment to quality mindset
Strong computer literacy and computer skills including Word, Excel, PowerPoint, Outlook
Canadian CMC Regulatory experience with small molecules, vaccines, and other biologics is an asset
Preferred Qualifications
Graduate degree and/or Post-Graduate Certificate in Regulatory Affairs.
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