Regulatory Affairs Specialist: Submissions and Compliance

8trive

Valenzuela

On-site

PHP 420,000 - 660,000

Full time

6 days ago
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Job summary

8trive in the Philippines is seeking a Regulatory Affairs professional to support regulatory documentation, submissions, and filing of accurate regulatory records.

Ideal candidates will have solid knowledge of regulatory compliance and requirements, and expertise in coordinating regulatory activities with regulators and internal teams.

Experience in regulated industries and familiarity with local Philippine regulations, as well as international frameworks (FDA, EMA, ISO), is a plus.

Qualifications

  • Strong skills in Regulatory Documentation and Regulatory Submissions to prepare and file records.
  • Solid knowledge of Regulatory Compliance and Regulatory Requirements to meet standards.
  • Expertise in Regulatory Affairs to coordinate activities with regulators and internal teams.
  • Experience in compliance, quality assurance, or legal support in regulated industries is beneficial.
  • Bachelor’s degree in related field or equivalent practical experience.
  • Strong analytical, documentation, and organizational skills with attention to deadlines.
  • Excellent verbal and written communication; able to work on-site with diverse teams.
  • Familiarity with local Philippine regulations and international frameworks (FDA, EMA, ISO) is a plus.

Skills

Regulatory Docs
Regulatory Submissions
Regulatory Compliance
Regulatory Requirements
Regulatory Affairs
Analytical Skills
Documentation
Organizational Skills
Communication

Education

Bachelor’s degree in Regulatory Affairs/Life Sciences/Pharmacy/Engineering/Law/Business

Job description

8trive in the Philippines is seeking a Regulatory Affairs professional to support regulatory documentation, submissions, and filing of accurate regulatory records.

Ideal candidates will have solid knowledge of regulatory compliance and requirements, and expertise in coordinating regulatory activities with regulators and internal teams.

Experience in regulated industries and familiarity with local Philippine regulations, as well as international frameworks (FDA, EMA, ISO), is a plus.

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