Regulatory Affairs Pharmacist

Centurion, South Africa | Full time | Hybrid | R1570534
Regulatory Affairs Pharmacist

Location: Johannesburg, South Africa
Contract Type: Fixed-Term Contract (12 Months)

About the Opportunity

IQVIA's client, a leading healthcare and pharmaceutical organisation, is seeking an experienced Regulatory Affairs Specialist to join their Regulatory team on a 12-month fixed-term contract based in Johannesburg.

This role will be responsible for managing regulatory activities across South Africa and selected Sub-Saharan African markets, ensuring compliance with applicable regulatory requirements while supporting product registrations, lifecycle management, and regulatory compliance initiatives.

Key Responsibilities

Manage product portfolios of registered products and products under review.
Compile and submit regulatory dossiers, including new product registrations, variations, renewals, and maintenance submissions.
Support New Chemical Entity (NCE), CTD, and electronic submissions.
Liaise with regulatory authorities and respond to regulatory queries.
Maintain regulatory licenses and ensure timely renewals.
Create and approve product artwork and labelling materials.
Ensure compliance with applicable regulations governing medicines, packaging, advertising, and promotion.
Monitor and communicate relevant regulatory intelligence and changes in legislation.
Support quality and compliance activities, including audits and SOP implementation.
Provide regulatory guidance and training to internal stakeholders where required.

Minimum Requirements

BPharm degree.
Registered with the South African Pharmacy Council (SAPC).
Minimum 3 years' experience in pharmaceutical regulatory affairs.
Proven experience with product registrations, variations, renewals, and dossier maintenance.
Working knowledge of:
eCTD
DocuBridge
SAHPRA Engagement Portal
FTP
Veeva Vault
Strong understanding of regulatory requirements for pharmaceuticals and lifecycle management.
Excellent communication, stakeholder management, and project management skills.
Strong attention to detail and ability to manage multiple priorities.

Preferred Experience

Experience working across South Africa and other Sub-Saharan African markets.
Knowledge of quality management systems and pharmaceutical compliance requirements.
Experience engaging directly with regulatory authorities.

What We're Looking For

The successful candidate will be a proactive, detail-oriented regulatory professional with strong technical expertise and the ability to work effectively across cross-functional teams. You will thrive in a fast-paced environment and be passionate about ensuring regulatory compliance while enabling successful product commercialisation.

Important Information

This is a 12-month fixed-term contract position based in Johannesburg, South Africa.

If you meet the above requirements and are looking for an opportunity to contribute to a dynamic healthcare environment, we encourage you to apply.

#LI-DNP #LI-CES

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work
Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.
Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.