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Regulatory Affairs

1 month ago

Fort Lauderdale, United States 5TH HQ LLC Full time
Job DescriptionJob Description

We are currently seeking a detail-oriented and motivated Regulatory Affairs Specialist. This role is crucial in ensuring that our products comply with all regulatory requirements. If you are passionate about regulatory affairs and looking for an opportunity to grow within a dynamic company, we encourage you to apply.

Responsibilities:

  • Prepare, review, and submit regulatory documents to ensure compliance with FDA and other regulatory authorities.
  • Maintain up-to-date knowledge of regulations, guidelines, and standards relevant to the pharmaceutical industry.
  • Assist in the preparation of regulatory submissions including New Drug Applications (NDAs), Investigational New Drug Applications (INDs), and amendments.
  • Coordinate with cross-functional teams to gather necessary information for regulatory submissions.
  • Ensure timely and accurate communication with regulatory authorities.
  • Monitor and track the progress of submissions and respond to any inquiries from regulatory bodies.
  • Assist in the development and implementation of regulatory strategies to support product approvals and lifecycle management.
  • Maintain accurate and organized regulatory files and records.

Requirements:

  • Bachelor’s degree in a related field such as biology, chemistry, or pharmaceutical sciences.
  • Previous experience in a regulatory affairs role within the pharmaceutical industry is preferred.
  • Strong understanding of FDA regulations and guidelines.
  • Excellent organizational and time management skills.
  • Strong attention to detail and ability to handle multiple projects simultaneously.
  • Effective communication skills, both written and verbal.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Ability to work independently and as part of a team.