Regulatory Affairs Associate

A Regulatory Affairs Associate supports the development and execution of regulatory strategies to ensure products meet all necessary legal and safety requirements. They prepare and manage regulatory documentation, interact with regulatory agencies, and contribute to the overall compliance of products with relevant laws and guidelines. 

• Documentation Management:

  Preparing, reviewing, and managing regulatory submissions and documentation, including those for clinical trials and product registrations.   

  • Submission Management:

    Overseeing the submission process to regulatory agencies and tracking submissions to ensure timely approvals.   

    Compliance Monitoring:

    Ensuring that products and processes comply with all relevant regulations and guidelines

    • Labeling and Packaging Review:

      Reviewing and approving product labeling, packaging, and advertising materials to ensure compliance.   

      Technical Skills

      Project Management

      Communication Skills

      Interpersonal Skills

       
     

    Adaptability