Regulatory Affairs - 573+ job offers

About the role We are seeking a highly motivated Regulatory Affairs Officer to join our dynamic team at Square Pharmaceutical, Inc' in Carmona Cavite. As a Regulatory Affairs Officer, you will play a crucial role in ensuring our pharmaceutical products meet all relevant regulatory requirements and s

Location This is a hybrid role. Our office is located at Arthaland Century Pacific Tower, 5th Avenue, BGC. This role requires going to our office at least one day a week. Role Hours The expected working hours for this position are from 12:00 AM to 9:00 AM, based on the Philippine Time Zone (PHT). Ab

Location This is a hybrid role. Our office is located at Arthaland Century Pacific Tower, 5th Avenue, BGC. This role requires going to our office at least one day a week. Role Hours The expected working hours for this position are from 12:00 AM to 9:00 AM, based on the Philippine Time Zone (PHT). Ab

Point Digital Finance, Inc.

Location This is a hybrid role. Our office is located at Arthaland Century Pacific Tower, 5th Avenue, BGC. This role requires going to our office at least one day a week. Role Hours The expected working hours for this position are from 12:00 AM to 9:00 AM, based on the Philippine Time Zone (PHT). Ab

PRIMARY OBJECTIVE The Regulatory Affairs Manager is responsible for leading and managing the Regulatory Affairs team in ensuring that all pharmaceutical products comply with applicable regulations in the Philippines. This role involves overseeing regulatory submissions, managing relationships with r

THE RGP CONSULTING EXPERIENCE RGP has a unique consulting model that provides opportunities for consultants to work in different ways. Most consultants work in a model where they have the flexibility and autonomy to choose projects aligning to their experience, skills and desired lifestyle. Other op

Main Function A Regulatory Affairs Associate is responsible for managing, coordinating, and documenting internal regulatory processes, which may include inspections, internal audits, license renewals, registrations, and several other processes under government regulations and ensure compliance of th

Job description: Main Function A Regulatory Affairs Associate is responsible for managing, coordinating, and documenting internal regulatory processes, which may include inspections, internal audits, license renewals, registrations, and several other processes under government regulations and ensure

Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dent

Regulatory Submissions: Prepare, review, and submit product registration applications for medical devices, diagnostic reagents, and medical equipment to the Philippine FDA. Compliance Monitoring: Ensure that all products comply with the regulatory requirements of the Philippine FDA, including standa

Regulatory Submissions: Prepare, review, and submit product registration applications for medical devices, diagnostic reagents, and medical equipment to the Philippine FDA. Compliance Monitoring: Ensure that all products comply with the regulatory requirements of the Philippine FDA, including standa

Drugmaker's Laboratories Inc.

Job Description Graduate of Bachelor of Science in Nursing Must be Registered Analytical and good in problem solving With at least one (1) year of work experience in FDA transactions or any similar job tasks. Computer literate and must have good interpersonal skills Job Type: Full-time Job Type: Ful

Job Summary: We are seeking a Regulatory Affairs Pharmacist to ensure compliance with local and international regulations in the animal healthcare industry . This role involves preparing and submitting regulatory documents for veterinary pharmaceuticals, vaccines, and other healthcare products while

Manages FDA licensing (medical devices and food), prepares and submits regulatory documents, and coordinates product registration with suppliers and internal teams. Ensures compliance, document control, and inspection readiness, while supporting inventory, labeling, and accreditation requirements. H

Duties & Responsibilities Assist in preparing all the technical documents required for submission to FDA and other regulatory agencies Responsible for ensuring that all product registrations, licenses, and certificates are valid and submitted to the FDA for renewal prior to the expiration date U