Lead regulatory submissions, health-authority liaison, and compliance activities from a hybrid pharmaceutical role in Kimberley, Northern Cape. CTD expertise matters.
This Regulatory Affairs Specialist supports cutting-edge therapies through accurate documentation and regulatory guidance. You will manage filings, review promotional materials, and contribute to product development and lifecycle strategies. Your work connects cross-functional teams with national and international regulatory expectations.
Key Responsibilities: Develop regulatory strategies for product development and lifecycle management
Review promotional materials against advertising regulations
Maintain regulatory databases and documentation systems
Participate in regulatory inspections and audits




Contribute to departmental SOPs and training materials
Requirements: Strong written and verbal communication skills
Analytical, problem-solving, and organizational capabilities
Three to five years’ regulatory affairs industry experience
Strong knowledge of global submission processes
Ability to work independently and collaboratively in hybrid teams
Bring regulatory submissions, lifecycle management, and clear communication skills to support compliant pharmaceutical access from Kimberley.

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📌 Regulatory Submissions Specialist Kimberley (British Columbia)
🏢 Placements24
📍 British Columbia