MSD

Specialist, Regulatory Affairs

MSD(3 days ago)

HybridFull TimeMedior$48,000 - $58,000Regulatory Affairs
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About this role

This role involves coordinating the product registration process to ensure compliance, approval, and proper documentation for market entry and product changes within the pharmaceutical industry. The focus is on supporting regulatory initiatives, maintaining compliance, and liaising with internal and external stakeholders.

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Required Skills

  • Regulatory Affairs
  • GMP
  • Regulatory Submissions
  • Documentation
  • Process Improvements
  • Compliance
  • Pharmaceutical Regulations
  • Cross-functional Communication
  • Project Management
MSD

About MSD

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