[FOR HIRE] Regulatory Affairs Specialist | SAHPRA | eCTD | Pharmacovigilance | Remote

Hi everyone,

I’m currently looking for remote, after-hours or weekend opportunities in Regulatory Affairs where I can add value to your team or projects.

I have solid experience as a Head of Regulatory Affairs in South Africa, working extensively with SAHPRA and international regulatory frameworks (ICH, WHO, PIC/S). I’ve managed full product lifecycles across human, veterinary, and medical device portfolios.

What I can help with:

eCTD publishing & lifecycle management

Dossier compilation (Modules 1–5)

SAHPRA submissions, variations & renewals

Pharmacovigilance systems (PSMF, safety reporting)

Quality Management Systems (QMS) & SOP development

Regulatory strategy & gap analysis

Audit & inspection readiness

Tools & systems:

Veeva Vault, Extedo, Lorenz DocuBridge

Strong MS Office & document management skills

I’ve successfully managed 30+ medicine dossiers, built compliant PV and QMS systems, and worked directly with health authorities.

I’m reliable, detail-oriented, and used to managing multiple projects under tight timelines. Open to freelance, consulting, or part-time remote work globally.

If you’re looking for support in regulatory submissions, compliance, or documentation — feel free to DM me or comment below.

Thanks!