Regulatory Pharmacist

Rivermed, Inc; Pasig; On-site; PHP 279,000 - 334,800; Full time

Job summary

A pharmaceutical company in Pasig is seeking a Regulatory Pharmacist responsible for preparing and submitting product registrations to the FDA. The ideal candidate is a licensed pharmacist with at least one year of regulatory affairs experience and strong communication skills. This full-time position offers a competitive salary of ₱25-30K monthly. Join us in ensuring compliance with local and international regulations.

Qualifications

• At least 1 year of experience in regulatory affairs or a related pharmaceutical role.
• In-depth knowledge of FDA regulations and product registration processes.
• Strong ability to manage multiple deadlines.

Responsibilities

• Prepare and submit product registration dossiers.
• Ensure compliance with local laws and regulations.
• Act as primary liaison with regulatory agencies.

Skills

Excellent communication skills

Documentation skills

Organizational skills

Attention to detail

Education

Licensed Pharmacist in the Philippines

Job description

Regulatory Pharmacist

Rivermed, Inc

Salary: ₱25-30K [Monthly] On-site - Pasig

Experience: 1-3 Yrs Exp

Bachelor Full-time

Job Description

• Prepare, review, and submit product registration dossiers to the FDA (Food and Drug Administration) and other relevant regulatory bodies.
• Ensure all products comply with local laws and regulations, including labeling, advertising, and marketing guidelines.
• Maintain up-to-date knowledge of current local and international regulatory requirements.
• Act as the primary liaison with regulatory agencies and respond to queries or audits as needed.
• Monitor and manage product renewals, amendments, and post-approval variations.
• Support quality assurance and pharmacovigilance functions, as needed.

Qualifications

• Licensed Pharmacist in the Philippines
• At least 1 year of experience in regulatory affairs or a related pharmaceutical role
• In-depth knowledge of FDA regulations, product registration processes, and other applicable laws
• Excellent communication, documentation, and organizational skills
• Strong attention to detail and the ability to manage multiple deadlines

Preferred Qualifications

• Experience with regulatory affairs in pharmaceuticals, and medical devices
• Familiarity with ASEAN CTD/ICH guidelines
• Background in quality assurance or product development is a plus

Working Location

Kapitolyo. Kapitolyo, Pasig, Metro Manila, Philippines

Posted on 27 June 2025

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Unfinanced / Angel

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Pharmaceutical

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