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Regulatory Affairs Assistant

Full-time

Global Quest Consulting Group, Inc.

Key Qualifications

  • Must be a Licensed Pharmacist.
  • With at least 1–2 years of relevant experience in Regulatory Affairs.
  • Experience in FDA processing and/or government bidding is required.
  • Knowledgeable in regulatory compliance and documentation.
  • Familiar with preparation and submission of regulatory requirements and permits.
  • Proficient in Microsoft Office applications and documentation management.
  • Detail-oriented with strong organizational and communication skills.
  • Able to work under pressure and meet deadlines with minimal supervision.

Job Responsibilities

  • Prepare, review, and submit regulatory documents to the FDA and other government agencies.
  • Monitor product registrations, renewals, licenses, and compliance requirements.
  • Ensure company compliance with applicable pharmaceutical and regulatory standards.
  • Coordinate with internal departments regarding regulatory concerns and documentation.
  • Handle government bidding requirements and related documentation
  • Maintain accurate records of permits, licenses, and regulatory submissions.
  • Monitor updates on FDA regulations and ensure timely implementation.
  • Perform other related duties that may be assigned from time to time.
Vacancy posted a month ago
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