Location: Midrand
Seeking a skilled professional to drive regulatory excellence in African markets.
Are you an experienced Regulatory Affairs Pharmacist with a strong understanding of medicines registration and compliance across African health authorities?
This role offers the opportunity to oversee registration processes, ensure product compliance, and contribute to a dynamic, fast-paced regulatory team.
Key Responsibilities:
Lead submission, renewal, and maintenance of pharmaceutical product registrations.
Conduct dossier evaluations and gap analyses for new and existing products.
Prepare and submit regulatory applications, ensuring compliance with health authority requirements.
Liaise with regulatory bodies to address inquiries and additional information requests.
Maintain accurate product records and databases in line with good documentation practices.
Review packaging, marketing materials, and product changes for compliance across multiple markets.
What You Bring:
✔️ Qualifications: B.Pharm degree.
✔️ Experience: 2–3 years in regulatory affairs (SADC, EAC preferred).
✔️ Skills: Strong knowledge of pharmaceutical legislation, meticulous document preparation, ability to interpret regulatory guidelines, and scientific reasoning.
✔️ Competencies: Detail-oriented, deadline-driven, strategic thinker with problem-solving skills and adaptability in a dynamic environment.
✔️ Technical Expertise: Proficiency in Microsoft Word, Adobe, and Excel for high-quality document production.
This is your chance to make an impact in a highly regulated, evolving industry while working with a team that values expertise and forward-thinking solutions.
Interested? Apply today and take the next step in your regulatory career!
Call Christine 084 627 3603 / christine@cbpro.co.za