Head of Regulatory Compliance

14 hours ago


Karachi, Sindh, Pakistan beBee Careers Full time
Regulatory Affairs Lead

This role is crucial for enabling compliant growth in both local and international markets by ensuring timely product registrations, smooth regulatory inspections, and effective lifecycle management of all dossiers.

The ideal candidate will possess a blend of deep regulatory expertise and strong cross-functional influence, especially across manufacturing, quality, supply chain, and business leadership.

Key Responsibilities:

  1. Lead end-to-end regulatory strategy and operations across all product categories and markets.
  2. Oversee registration, renewal, and variation submissions for DRAP and relevant global authorities.
  3. Ensure all dossiers (local and international) are compliant, audit-ready, and continuously updated.
  4. Partner closely with R&D, manufacturing, and quality teams to ensure regulatory readiness and alignment.
  5. Coordinate with international teams or partners on regulatory submissions for export markets.
  6. Manage regulatory audits, inspections, and correspondence with authorities, ensuring transparent and timely engagement.
  7. Build and strengthen internal regulatory systems, SOPs, and document management tools.
  8. Stay ahead of evolving local and international regulatory frameworks and lead internal adaptations.
  9. Support regulatory inputs into product development, new launches, and business expansions.

What You'll Bring:

  • 10+ years of experience in regulatory affairs within the pharmaceutical industry.
  • In-depth understanding of DRAP processes and documentation requirements.
  • Experience managing product lifecycles across both domestic and export markets.
  • Proven ability to lead teams and influence cross-functionally across technical and commercial domains.
  • Strong documentation, compliance, and stakeholder management skills.
  • Familiarity with global regulatory frameworks (e.g., WHO PQ, GCC, ASEAN, etc.) is a plus.


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