Oversee regulatory compliance and documentation processes for pharmaceutical products.

• Coordinated internal audits and inspections, ensuring adherence to regulatory standards and timely resolution of compliance issues.
• Compiled and prepared submission materials for FDA and EMA, resulting in a 95% approval rate for new product registrations.
• Developed and implemented internal training programs on regulatory requirements, enhancing team knowledge and operational efficiency.

Assisted in the preparation and submission of regulatory documents for medical devices.

• Conducted thorough reviews of product labeling and promotional materials to ensure compliance with regulatory guidelines.
• Collaborated with cross-functional teams to streamline the submission process, reducing time to market by 20%.
• Maintained up-to-date knowledge of regulatory changes and communicated impacts to stakeholders.