Regulatory Affairs Executive - Abbott Pharmaceuticals (Third-party contract)

Job description

JOB DESCRIPTION:ABOUT ABBOTT Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. WORKING AT ABBOTT At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: Career development with an international company where you can grow the career you dream of. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. ROLES & RESPONSIBILITIES MAIN PURPOSE OF ROLE Responsible for supporting regulatory lifecycle management activities for Abbott products in Vietnam, including preparation and submission of variation dossiers, maintenance of regulatory documentation and databases, and coordination of regulatory change implementation to ensure compliance with local regulations and business timelines. MAIN RESPONSIBILITIES Prepare and submit variation dossiers for assigned AHVN products to the Drug Administration of Vietnam (DAV). Maintain accurate and complete regulatory documentation, including electronic and hard-copy archiving of submissions and approvals. Coordinate with cross-functional stakeholders to support regulatory Management of Change (MOC) implementation and ensure timely completion of action items. Track and maintain regulatory databases, registration trackers and submission records to ensure data integrity and compliance. Support ongoing regulatory maintenance activities to ensure continuous compliance of marketed products with local regulatory requirements. Perform other duties and responsibilities as assigned by the manager to support regulatory operations, business objectives and organizational priorities. MINIMUM BACKGROUND/ EXPERIENCE REQUIRED Bachelor's Degree in pharmacy or Registered Pharmacist in Vietnam Knowledge of regulations and standards. From 2 years relevant experience in regulatory affairs. Good English communication Proficient working with systems and managing large volumes of data. Compliance mindset The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted. JOB FAMILY:Regulatory Operations DIVISION:EPD Established Pharma LOCATION:Vietnam > Hanoi : Handi Resco Tower ADDITIONAL LOCATIONS: WORK SHIFT:Standard TRAVEL:Not specified MEDICAL SURVEILLANCE:Not Applicable SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)