Regulatory Affairs

Regulatory Affairs

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Farbe Firma Pvt. Ltd.

time outline iconAnkleshwar, Gujarat, India

Posted on 27-11-2025

1 Vacancy

Description

  • Prepare, review, and submit regulatory documents for product approvals, renewals, and variations.
  • Ensure compliance with national and international regulatory guidelines (e.g., FDA, EMA, CDSCO).
  • Coordinate with R&D, QA, QC, and production teams to gather required data for submissions.
  • Maintain up-to-date knowledge of regulatory laws, standards, and industry changes.
  • Review product labels, artwork, and packaging for regulatory compliance.
  • Communicate with regulatory authorities regarding queries, audits, and inspections.
  • Maintain regulatory databases, documentation, and submission records.
  • Support product registration, licensing, and certification processes across markets.
  • Assist in managing regulatory risks and ensuring timely compliance with changing regulations.

Category

Pharmaceuticals

Key Skills

CommunicationTeam WorkStrategic ThinkingMultitaskingAttention to Detail

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