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 20 days ago
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