Regulatory Affairs
Global Quest Consulting Group
Job Description
- Ensure company products and processes comply with applicable laws, regulations, standards, and guidelines (e.g., health authority, procurement, and quality regulations).
- Monitor changes in regulatory and compliance requirements and assess their impact on existing and new products.
- Support internal audits, regulatory inspections, and compliance reviews.
- Maintain proper document control systems, SOPs, and compliance records.
- Prepare, compile, review, and maintain regulatory dossiers in compliance with local and international regulatory requirements.
- Manage product registration, renewal, variation, and amendment submissions with relevant regulatory authorities.
- Licensed Pharmacist
- Preferably with 1-2 years of experience in regulatory affairs or FDA registration of pharmaceutical or medical supplies
- Knowledgeable in regulatory documentation, product registration, compliance processes, and government hospital bidding.
- Computer literate and highly organized, with strong analytical and problem-solving skills.
- Excellent communication, coordination, and leadership abilities.
- Proactive, detail-oriented, and capable of handling multiple tasks efficiently.
- Willing to be assigned in Greenhills, San Juan City, Metro Manila.
- Salary : Negotiable
Avie Vinalon
RecruiterGlobal Quest Consulting Group
More than ten replies today
Posted on 15 Jan 2026
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