Regulatory Affairs Specialist — Veterinary & Animal Health

PLARIDEL PRODUCTS & SERVICES, INC.; Bulacan; On-site; PHP 420,000 - 600,000; Full time

Job summary

PLARIDEL PRODUCTS & SERVICES, INC. in the Philippines (Bulacan) is seeking a Regulatory Affairs Specialist to manage product registration, licensing, and compliance for veterinary drugs, biologics, feed additives, and related animal health products.

You will coordinate with government agencies, monitor status, review labels and packaging for regulatory approval, maintain regulatory documentation, and provide cross-functional regulatory support.

Qualifications

• Graduate of a related life science course.
• Licensed Pharmacist preferred.
• At least 2 years of regulatory affairs experience in animal health or veterinary pharmaceuticals.
• Familiarity with BAI, FDA, and government agency regulations is a plus.
• Strong written and verbal communication.
• Highly organized and able to manage multiple projects.

Responsibilities

• Prepare and submit product registration and licensing applications for veterinary drugs, biologics, feed additives, and other animal health products.
• Coordinate with regulatory authorities and monitor application status.
• Ensure compliance with applicable regulatory requirements and company standards.
• Maintain and update regulatory documentation and databases.
• Assist in reviewing product labels, packaging materials, and promotional claims for regulatory compliance.
• Provide regulatory support to internal departments and business partners.

Skills

Strong communication

Organized

Detail-oriented

Project management

Education

Life science degree

Pharmacist license preferred

Job description

PLARIDEL PRODUCTS & SERVICES, INC. in the Philippines (Bulacan) is seeking a Regulatory Affairs Specialist to manage product registration, licensing, and compliance for veterinary drugs, biologics, feed additives, and related animal health products.

You will coordinate with government agencies, monitor status, review labels and packaging for regulatory approval, maintain regulatory documentation, and provide cross-functional regulatory support.