Lead pharmaceutical regulatory submissions in Kimberley using detailed compliance knowledge and solid communication skills. Coordinate approvals across local and international requirements.
This experienced Regulatory Affairs Specialist manages regulatory activities for pharmaceutical products. The position covers product registration, variations, post-market surveillance, and regulatory guidance. You will support timely approval and market access while working within a dedicated regulatory team.
Key Responsibilities: Prepare and submit product registration applications
Manage regulatory applications for product variations
Liaise with SAHPRA regarding submissions and inquiries
Review promotional materials for regulatory compliance




Monitor legislation and assess impacts on products
Requirements: Bachelor's degree in Pharmacy, Life Sciences, Chemistry, or related field
Minimum four years' pharmaceutical regulatory affairs experience
Knowledge of South African regulatory submission requirements
Understanding of key international market requirements
Experience with regulatory databases and submission software
Apply pharmaceutical regulatory expertise, submission management, and analytical skills to support compliant market access in Kimberley.

#J-18808-Ljbffr

📌 Pharmaceutical Regulatory Affairs Specialist (British Columbia)
🏢 Placements24
📍 British Columbia