Are you ready to shape the regulatory landscape for life‑saving medicines in South Africa? Join us in a role where your expertise will directly influence how patients living with serious chronic diseases gain timely access to the treatments they need. If you're passionate about regulatory excellence and want to be part of a team driving real impact, read on and apply today.

Johannesburg, Gauteng, ZA

Category: Reg Affairs & Safety Pharmacovigilance

As our new Regulatory Affairs Portfolio Manager, you will play a key role in compiling, submitting and securing approval for New Drug Applications (NDA) and Life Cycle Management (LCM) licences, while ensuring that Novo Nordisk remains fully compliant with the evolving South African regulatory environment. Working under the supervision of the RA Manager, you will be a trusted partner across the affiliate and a credible voice with local Health Authorities.

Your day‑to‑day responsibi...