📢 New: get today's jobs on our WhatsApp Channel
Jobiglo

No results.

Senior Manager: RA Strategy & Innovation

PSM Personnel

New
Senior 🇬🇧 English
Regulatory strategy Regulatory intelligence Regulatory lifecycle management Regulatory due diligence Clinical data assessment

Job description

About the role

The client, a leading pharmaceutical company, seeks a Senior Manager to provide strategic regulatory leadership for innovative and complex medicine portfolios. You will shape regulatory pathways, assess benefit‑risk evidence and influence development, registration and market‑access decisions.

Key responsibilities

  • Develop and lead regulatory strategies for NCEs, biologics, biosimilars, complex generics, peptides and advanced therapies.
  • Critically assess clinical, non‑clinical, safety, quality and benefit‑risk data to support registrations, variations, waivers and lifecycle decisions.
  • Provide regulatory intelligence on SAHPRA, reliance pathways, labeling and local documentation requirements.
  • Lead engagements with regulatory authorities, scientific advice meetings, query responses and waiver requests.
  • Conduct regulatory due diligence for licensing, in‑licensing, acquisitions and partnership opportunities.
  • Collaborate with Medical, Pharmacovigilance, Quality, R&D, Commercial, Supply Chain and global regulatory teams.

Required profile

  • Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, Medicine, Toxicology, Biotechnology or related field.
  • 10–12 years of regulatory affairs experience, preferably with pharmaceutical, biological or complex product portfolios.
  • At least 5 years in a strategic regulatory role covering product strategy, clinical data assessment, lifecycle management and authority engagement.
  • Proven experience with NCEs, biologics, biosimilars or complex generics supported by clinical data.
  • Strong knowledge of SAHPRA, ICH, EMA and WHO regulatory requirements and direct experience engaging with SAHPRA.

Required skills

  • Regulatory strategy development and implementation.
  • Regulatory intelligence and due‑diligence analysis.
  • Clinical data assessment and benefit‑risk evaluation.
  • CMC expertise (Module 3, comparability, site readiness, post‑approval variations).
  • Engagement with regulatory authorities and scientific advice processes.

Questions fréquentes

Le salaire n'est pas communiqué publiquement par le recruteur. Vous pouvez postuler et négocier directement avec PSM Personnel.
Cliquez sur "Postuler maintenant" en haut de la page. Vous pouvez importer votre CV en 1 clic — Jobiglo extrait automatiquement vos informations et postule pour vous.

Why are you reporting this job?

Thank you for your report. We will review this job.

Explore further

Salaries, guides and searches in South Africa.

Apply in 30 seconds

Enter your email to apply. An account will be created automatically.

Apply now →

By continuing, you accept our terms of use.

Already have an account? Login

A question about this job?

Ask it here: you will get the full job summary by e-mail, right away.

💬 Chat with us on Telegram

Published 18 hours ago

Expires 1 month from now

8 views · 0 interested

Boost your chances

Upload your CV — we will match you with relevant openings.

Analyzing your CV...

PSM Personnel