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 creative 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.

📌 Regulatory Submissions Specialist Kimberley
🏢 Placements24
📍 Kimberley