International Labeling Support Specialist

Merck & Co., Inc.

Hybrid
Minimum 2-3 years pharmaceutical industry experience
Experience in regulatory affairs labeling and artwork
Proficiency in microsoft 365 applications
The position of International Labeling Support Specialist at Merck & Co., Inc. involves managing and executing regulatory operational activities related to labeling and artworks in compliance with company standards. The role requires collaboration across various functions and regions, focusing on process improvement and operational excellence within the pharmaceutical industry

Job Summary

  • The Specialist will partner cross-functionally to ensure all labeling and artwork regulatory activities are planned, managed, and executed timely and accurately.
  • Responsibilities include preparing high-quality labeling packages, maintaining databases, and supporting country regulatory affairs with necessary filings.
  • The role requires contributing to process improvements, re-engineering initiatives, and collaborating with global teams on CMC changes and product launches.

Matching Summary

Match Score: 85

The position of International Labeling Support Specialist at Merck & Co., Inc. involves managing and executing regulatory operational activities related to labeling and artworks in compliance with company standards. The role requires collaboration across various functions and regions, focusing on process improvement and operational excellence within the pharmaceutical industry.

Skills & Requirements

Must-have

  • Minimum 2-3 years pharmaceutical industry experience
  • Experience in regulatory affairs labeling and artwork
  • Proficiency in Microsoft 365 applications
  • Ability to work cross-functionally in matrix environment
  • Strong organizational and detail-oriented skills

Nice-to-have

  • Knowledge of operational excellence principles
  • Interest in new tools and automation
  • Design thinking and innovative mindset
  • Familiarity with local regional legislation frameworks
  • Master's degree in related field

Key Requirements

  • Bachelor's degree in life science or related field
  • 2-3 years minimum experience in pharmaceutical industry
  • Previous experience in Regulatory Affairs or Quality
  • No visa sponsorship available

Work Rights

Not specified

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