Regulatory Affairs Pharmacist

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

Company Description

Largen Med Inc., established in 1994, is a Filipino pharmaceutical company focused on the discovery, research, and marketing of effective immunity and disease prevention supplements and prescription medicines. The company emphasizes ethically promoted products designed to support patient compliance and convenience. Its work is guided by a framework built on a united team of professional, responsible, motivated, and disciplined individuals. Largen Med Inc. is committed to advancing the welfare of Filipino patients through high-quality pharmaceutical solutions and continuous innovation.

Role Description

The Regulatory Affairs Pharmacist is a full-time, on-site role based in Quezon City. This role is responsible for preparing, reviewing, and submitting regulatory documents to ensure compliance with national and international pharmaceutical regulations. The individual monitors updates to regulatory requirements, interprets guidelines, and advises internal teams on implications for product development, labeling, and marketing. Daily tasks include maintaining regulatory files, coordinating with manufacturing, quality, and marketing teams, and supporting audits and inspections. The role also involves communicating with regulatory authorities, addressing queries, and contributing to the development and implementation of regulatory strategies for new and existing products.

Qualifications

• Strong knowledge and practical experience in Regulatory Affairs, including understanding and application of Regulatory Requirements and Regulatory Compliance.
• Licensed Pharmacist with solid grounding in Pharmacy practice, preferably with experience in pharmaceutical or healthcare industry.
• Excellent Communication skills, both written and verbal, for effective interaction with regulators, internal teams, and external partners.
• Ability to interpret and apply relevant laws, guidelines, and standards; strong attention to detail and document accuracy.
• Proficiency in documentation management and use of basic office software; strong organizational and time management skills.
• Capacity to work collaboratively in multidisciplinary teams and make sound, ethical decisions aligned with patient welfare.
• Experience with product registration, labeling review, and regulatory submissions in the Philippines is an advantage.
• Relevant bachelor’s degree in Pharmacy or a related field; additional training in regulatory affairs or quality systems is beneficial.