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.

📌 Pharmaceutical Regulatory Affairs Specialist (Kimberley)
🏢 Placements24
📍 Kimberley