To provide support to the RA department to ensure timely submissions and approvals of amendments in line with the submission plan and to meet regulatory objectives.
About The Role
Major accountabilities:
- Understanding the Medicine Act and Pharmacy Act and the related Regulations and guidelines and how these influence the Regulatory Environment.
- Understanding the elements of the Marketing Code.
- Preparation and submissions of regulatory applications to SAHPRA.
- Proof reading of artwork components.
- Supporting compliance activities within the RA team
- Being an active member of the RA team, participating in all team activities, meetings and gathering.
- Support the RA team to meet its overall objectives.
Education:
- Science degree with Honours or masters degree.
- Exposure to Regulatory Sciences or experience in Regulatory Affairs will be an advantage.
- Strong interpersonal and communication skills.
- Highly organized.
- Self-starter.
- Ability to manage multiple projects and consistently meet deadlines.
- Your application must be supported by a motivational letter and your academic transcripts
- Must be a South African Citizen.
- Ages between 18 - 35 Years.
- English.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards







