Regulatory Affairs Pharmacist

GlaxoSmithKline

Johannesburg, South Africa
Hybrid
Manage regulatory submissions
Product lifecycle activities
Maintain compliance
You will manage regulatory submissions for new product applications and product lifecycle activities and support cross-functional teams to maintain compliance with local regulatory requirements

Job Summary

  • You will manage regulatory submissions for new product applications and product lifecycle activities and support cross-functional teams to maintain compliance with local regulatory requirements.
  • This role offers progression, meaningful impact and the chance to help GSK unite science, technology and talent to get ahead of disease together.
  • You will join a team that supports your development through on-the-job learning and formal regulatory training.

Matching Summary

You will manage regulatory submissions for new product applications and product lifecycle activities and support cross-functional teams to maintain compliance with local regulatory requirements.

Skills & Requirements

Must-have

  • manage regulatory submissions
  • product lifecycle activities
  • maintain compliance
  • SAHPRA regulations
  • document control
  • change control processes

Nice-to-have

  • ambitious for patients
  • accountable for impact
  • doing the right thing
  • clear thinking
  • practical problem solving
  • collaboration
  • focus on patient safety

Key Requirements

  • Bachelor of Pharmacy (B.Pharm) or equivalent
  • current registration with the South African Pharmacy Council
  • Minimum 3 years’ experience
  • pharmaceutical product registration
  • regulatory affairs
  • preparing CMC submissions
  • Good written and verbal communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter