Regulatory Affairs Manager Pharmacist
Location: N JHB
Ref: MVG/RA-NJ
We're Hiring: Regulatory Affairs Manager | Gauteng
Are you a seasoned Regulatory Affairs professional ready to take the lead in ensuring compliance and driving successful product registrations across multiple territories? An exciting opportunity has opened up for a Regulatory Affairs Manager to join a dynamic team within the pharmaceutical sector. Reporting to the Head of Regulatory Affairs, you'll be instrumental in providing strategic regulatory oversight, managing a portfolio of products, and engaging with both internal stakeholders and external regulatory bodies.
What You'll Bring:
- A degree or diploma in Pharmacy with SAPC registration
- 5+ years' experience in Regulatory Affairs (preferably human medicines)
- Strong understanding of the product development lifecycle
- Project management expertise and cross-functional collaboration skills
- Hands-on experience with CTD/eCTD submissions
- Prior RA Management experience leading a small team
Key Responsibilities:
- Manage end-to-end regulatory submissions (new applications & maintenance)
- Liaise with SAHPRA, other MRAs, and 3rd party partners
- Allocate resources, set priorities, and ensure compliance with evolving regulations
- Maintain internal training, mentor junior staff, and support audits/inspections
- Keep up to date with relevant legislation and regulatory trends
What Makes You Stand Out:
- Strategic mindset with the ability to work under pressure
- Excellent leadership, decision-making, and problem-solving skills
- Passion for quality, compliance, and continuous improvement
If you thrive in a fast-paced, collaborative environment and want to play a key role in bringing medicines to market - this could be the next step in your career.
Interested? Send your CV to response "at" [URL Removed] or apply online.
Desired Skills:
Desired Work Experience:
Desired Qualification Level & Accreditations: