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 innovative 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:
Solid written and verbal communication skills
Analytical, problem-solving, and organizational capabilities
Three to five years’ regulatory affairs industry experience
Robust knowledge of global submission processes
Ability to work independently and collaboratively in hybrid teams

Bring regulatory submissions, lifecycle management, and explicit communication skills to support compliant pharmaceutical access from Kimberley.

📌 Regulatory Submissions Specialist Kimberley (Canada)
🏢 Placements24
📍 Canada