Job Summary

• Lead the development, revision, review, agreement, and maintenance of primary labeling for assigned compounds.
• Contribute to the global labeling strategy, including understanding competitors and labeling aspects for development.
• Ensure high quality and compliant labeling documents and contribute to continuous improvement of the end-to-end labeling process.

Matching Summary

Salary

Base: $117,000.00 - $201,250.00; Bonus/Equity: Eligible for annual performance bonus and long-term incentive program; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Key Requirements

• Bachelor's degree in a scientific discipline
• 4 years of relevant pharmaceutical industry experience
• 3 years of Regulatory Affairs experience in product labeling/labeling regulations preferred
• Experience discussing and communicating scientific concepts
• Basic understanding of worldwide regulatory guidelines for labeling
• Experience leading project teams in a matrix environment
• Experience participating in continuous improvement projects
• Experience working with document management systems

Work Rights