Regulatory Affairs Officer

Global Quest Consulting Group; Quezon City; On-site; PHP 350,000 - 550,000; Full time

Job summary

Global Quest Consulting Group in Quezon City is seeking a Regulatory Affairs Officer responsible for ensuring pharmaceutical products comply with local and international regulatory requirements. You will prepare, submit, and maintain product registrations and licenses with authorities such as the FDA, and ensure adherence to applicable laws and guidelines.

The role requires a Pharmacy degree, a valid PRC license, and 1–3 years of regulatory affairs experience, with strong attention to detail,

Qualifications

• Bachelor’s degree in Pharmacy and licensed pharmacist.
• Registered Pharmacist with a valid PRC license.
• 1–3 years of experience in regulatory affairs (preferred).
• Strong knowledge of pharmaceutical regulations and FDA requirements.
• Excellent attention to detail and organizational skills.
• Good communication and coordination skills.
• Proficient in documentation and regulatory submission processes.

Responsibilities

• Ensure pharmaceutical products comply with local and international regulatory requirements.
• Prepare, submit, and maintain product registrations and licenses with regulatory authorities such as the FDA.
• Ensure adherence to applicable laws and guidelines.

Skills

Regulatory knowledge

Attention to detail

Organizational skills

Communication skills

Documentation & submission

Education

Bachelor’s degree in Pharmacy

Job description

On-site - Quezon City 1-3 Yrs Exp Diploma Full-time

Job Description

Job Summary:

The Regulatory Affairs Officer is responsible for ensuring that pharmaceutical products comply with all local and international regulatory requirements. The role involves preparing, submitting, and maintaining product registrations and licenses with regulatory authorities such as the Food and Drug Administration and ensuring adherence to applicable laws and guidelines.

Qualifications

• Bachelor’s Degree in Pharmacy (Licensed Pharmacist).
• Registered Pharmacist with a valid PRC license.
• With at least 1-3 years of experience in regulatory affairs (preferred).
• Strong knowledge of pharmaceutical regulations and FDA requirements.
• Excellent attention to detail and organizational skills.
• Good communication and coordination skills.
• Proficient in documentation and regulatory submission processes.