Regulatory Affairs Specialist – Pharma Submissions & Lifecycle

A leading pharmaceutical company in Midrand, Gauteng is looking for a Regulatory Affairs Specialist to manage regulatory submissions and lifecycle activities for pharmaceutical products. Candidates should have a Bachelor of Pharmacy and at least three years of experience in Regulatory Affairs. This full-time role requires proficiency with DocuBridge and a strong focus on compliance and communication. The successful applicant will contribute to bringing life-changing medicines to market efficiently.
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