Manager Qrem & Pharmacovigilance

Fresenius Medical Care

Pakistan
Medical device and drug registration in pakistan
Liaising with drap health authority agencies
Pharmacovigilance responsible person duties
The role involves managing product-related regulatory and quality activities including drug and device registration in Pakistan

Job Summary

  • The role involves managing product-related regulatory and quality activities including drug and device registration in Pakistan.
  • Candidates will serve as the Pharmacovigilance Responsible Person, overseeing safety reporting and compliance with local regulations.
  • Fresenius Medical Care offers a corporate culture that encourages innovative thinking and professional development within a global team.

Matching Summary

The role involves managing product-related regulatory and quality activities including drug and device registration in Pakistan.

Skills & Requirements

Must-have

  • Medical Device and Drug registration in Pakistan
  • Liaising with DRAP health authority agencies
  • Pharmacovigilance responsible person duties
  • Quality Management System implementation
  • Customer complaint handling and reporting
  • GMP and GDP compliance knowledge

Nice-to-have

  • Solution-oriented mindset for regulatory issues
  • Strong stakeholder management skills
  • Experience with ISO 31000 standards
  • Knowledge of MedTech sector trends
  • Ability to work with minimal supervision

Key Requirements

  • Degree in Pharmacy, Chemical, Bioengineering, or Health Professional
  • At least 8 years of industrial experience in Medical Device or healthcare industry
  • Comprehensive expertise in South Asia regulatory requirements
  • Fluency in English written and spoken

Work Rights

Not specified

Tailored Resume

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