Minimum 2-3 years pharmaceutical industry experience
Experience in regulatory affairs labeling and artwork
Proficiency with microsoft 365 apps excel powerpoint sharepoint
The Specialist will partner cross-functionally to ensure all labeling and artworks regulatory operational activities are planned, managed, and executed timely and accurately
Job Summary
The Specialist will partner cross-functionally to ensure all labeling and artworks regulatory operational activities are planned, managed, and executed timely and accurately.
Responsibilities include preparing high-quality labeling packages aligned with company requirements and supporting country regulatory affairs on database maintenance and records filings.
The role requires contributing to process improvement initiatives and collaborating with global and regional teams for labeling queries and project coordination.
Matching Summary
The Specialist will partner cross-functionally to ensure all labeling and artworks regulatory operational activities are planned, managed, and executed timely and accurately.
Skills & Requirements
Must-have
Minimum 2-3 years pharmaceutical industry experience
Experience in Regulatory Affairs labeling and artwork
Proficiency with Microsoft 365 apps Excel PowerPoint SharePoint
Nice-to-have
Interest in new tools or automatization
Innovative mindset and design thinking skills
Familiarity with local and regional legislation frameworks
Key Requirements
Bachelor's degree in life science engineering business or related field
Master's degree desired
Previous experience in Regulatory Affairs CMC compliance management or quality