Regulatory Affairs Associate (Temporary Contract - 6 Months)

• Assist in the preparation and submission of regulatory documentation for new product registrations and variations, ensuring adherence to global health authority guidelines. • Support the maintenance of regulatory databases and submission tracking systems, ensuring data accuracy and completeness for ongoing compliance. • Conduct literature searches and gather scientific information to support regulatory submissions and respond to health authority queries. • Review product labeling and promotional materials for compliance with applicable regulations and company policies. • Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or a related scientific field. • Minimum of 1-2 years of experience in a regulatory affairs role within the pharmaceutical or medical device industry. • Familiarity with global regulatory submission processes (e.g., FDA, EMA). • Proficiency in using regulatory information management systems (RIMS) and document management systems.