Regulatory Affairs Specialist

* KEY RESPONSIBILITIES*

1. *Technical Support*: Provide comprehensive technical assistance for the legal and registration activities of the Regulatory Affairs Department

2. *FDA Registration*: Prepare, compile, and submit high-quality registration dossiers to the Food and Drug Administration (FDA)

3. *Compliance Monitoring*: Ensure all products, documentations, and corporate operations strictly comply with current mandates from specific regulatory agencies

4. *Liaison Functions*: Act as a reliable point of contact between the company and government regulatory bodies

* QUALIFICATIONS*

- *Education*: Graduate of Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or any Life Sciences course

- *Experience*: Minimum 1 to 2 years of solid working experience in a regulatory affairs role

- *Domain Advantage*: Prior experience in handling FDA registrations for BOTH medical devices and pharmaceuticals is highly preferred

* WORK DETAILS*

- *Location*: Makati City

- *Schedule*: Monday to Friday, 8:00 AM to 5:00 PM

- *Requirement*: Willingness to conduct field work for government agency transactions