REGULATORY PHARMACIST

PHILIPPINE UNITED PHARMA CORP.; Carmona; On-site; PHP 446,000 - 781,000; Full time

Job summary

PHILIPPINE UNITED PHARMA CORP. in Cavite, Philippines, seeks two licensed pharmacists to join regulatory affairs, handling product registration and ensuring compliance with government regulations.

You will coordinate with FDA/PRC, prepare regulatory documents, monitor changes, and support renewal of licenses. Candidates should be PRC-registered pharmacists with drug registration experience and strong documentation skills; MS Office proficiency is required.

Qualifications

• Licensed pharmacist with PRC registration.
• Experience in drug registration and regulatory affairs.
• Knowledgeable in FDA regulations and product registration.
• Strong documentation skills and attention to detail.
• Proficient with MS Office applications.
• Able to work independently and meet deadlines.

Responsibilities

• Handle product registration and regulatory submissions.
• Coordinate with government agencies for permits, licenses, and product approvals.
• Prepare, review, and maintain regulatory documents and records.
• Monitor regulatory requirements and ensure compliance.
• Assist in renewal of licenses, registrations, and certifications.
• Support quality assurance and regulatory compliance activities.
• Perform other duties related to regulatory affairs.

Skills

Regulatory affairs

Documentation

Drug registration

Attention to detail

Independent work

FDA regulations

Regulatory compliance

Education

Bachelor of Pharmacy

Tools

MS Office

Job description

We are looking for two (2) licensed pharmacists who will be responsible for regulatory affairs, product registration, and ensuring compliance with government regulations related to pharmaceutical products.

• Licensed Pharmacist (PRC Registered)
• Graduate of Pharmacy or any related course with experience in drug registration and regulatory affairs
• Knowledgeable in FDA regulations, product registration, and documentation
• Strong attention to detail and documentation skills
• Computer literate (MS Office applications)
• Able to work independently and meet deadlines
• Experience in a pharmaceutical company is an advantage

DUTIES & RESPONSIBILITIES

• Handle product registration and regulatory submissions
• Coordinate with government agencies regarding permits, licenses, and product approvals
• Prepare, review, and maintain regulatory documents and records
• Monitor regulatory requirements and ensure company compliance
• Assist in the renewal of licenses, registrations, and certifications
• Support quality assurance and regulatory compliance activities
• Perform other duties related to pharmaceutical regulatory affairs