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Regulatory Affairs professional with 2.5 years of experience in CRO and pharmaceutical submissions. Skilled in CTD/eCTD dossier preparation, global compliance (EMEA, APAC, NA, LATAM) and regulatory documentation. Hands-on expertise in Raw material specifications, packaging documentation, and regulatory databases. Recognized for process excellence, accuracy, and cross- functional collaboration. Completed a Certified Regulatory Affairs course to strengthen knowledge of global regulations.

Experienced with managing document workflows and ensuring compliance with relevant standards. Utilizes advanced document management software to streamline processes and maintain accuracy. Track record of effectively collaborating with team members and adapting to evolving requirements.
Professional with strong experience in managing and organizing documentation processes and systems. Known for reliability, adaptability, and results-driven approach. Skilled in maintaining accurate records, ensuring compliance, and facilitating seamless team collaboration. Proven ability to thrive in fast-paced environments while maintaining high standards and flexibility.

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