Regulatory Affairs Pharmacist — Compliance & Strategy Lead

Largen Med Inc.; Quezon City; On-site; PHP 600,000 - 1,000,000; Full time

Job summary

Largen Med Inc. is seeking a Regulatory Affairs Pharmacist for a full-time, on-site role in Quezon City.

You will prepare, review, and submit regulatory documents to ensure compliance with national and international pharmaceutical regulations. You will monitor regulatory updates, interpret guidelines, advise internal teams on product development, labeling, and marketing, and coordinate with manufacturing, quality, and marketing.

Qualifications

• Strong knowledge of Regulatory Affairs and compliance requirements.
• Licensed Pharmacist with pharmacy practice background.
• Excellent written and verbal communication for regulators and teams.
• Ability to interpret laws, guidelines, and standards with attention to detail.
• Proficiency in documentation management and basic office software.
• Collaborative mindset and ethical decision-making prioritizing patient welfare.
• Experience with product registration, labeling review, and regulatory submissions in the Philippines is an advantage.
• Bachelor’s degree in Pharmacy; additional regulatory affairs training is beneficial.

Responsibilities

• Prepare, review, and submit regulatory documents to ensure compliance.
• Monitor regulatory requirements and interpret guidelines for product development.
• Maintain regulatory files and coordinate with manufacturing, quality, and marketing teams.
• Support audits and inspections and communicate with regulatory authorities.
• Contribute to regulatory strategies for new and existing products.

Skills

Regulatory affairs knowledge

Regulatory interpretation

Communication skills

Attention to detail

Documentation management

Team collaboration

Ethical decision-making

Education

Bachelor's degree in Pharmacy

Job description

Largen Med Inc. is seeking a Regulatory Affairs Pharmacist for a full-time, on-site role in Quezon City.

You will prepare, review, and submit regulatory documents to ensure compliance with national and international pharmaceutical regulations. You will monitor regulatory updates, interpret guidelines, advise internal teams on product development, labeling, and marketing, and coordinate with manufacturing, quality, and marketing.