Asst. Manager-Regulatory Affairs

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Asst. Manager-Regulatory Affairs

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

Abryl Laboratories

time outline iconDera Bassi, Punjab, India

Posted on 24-12-2024

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1 Vacancy

Description

  • Ensure all products meet regulatory requirements for approval in domestic and international markets.
  • Liaise with regulatory bodies to ensure the submission process is smooth and compliant.
  • Prepare and submit regulatory applications, dossiers, and documents.
  • Monitor regulatory developments and trends to keep the organization up-to-date with the latest regulatory changes.
  • Prepare and review regulatory submission documents, ensuring accuracy and completeness.
  • Maintain and organize regulatory files, ensuring all documentation is up-to-date and readily accessible for audits or inspections.
  • Coordinate and manage the preparation of dossiers for product registrations with appropriate regulatory authorities.
  • Draft and review labeling, packaging, and advertising materials to ensure compliance with applicable regulations.

Category

Pharmaceuticals

Functional Area

Regulatory Affairs / Pharmacovigilance

Key Skills

Attention to DetailProblem solvingCommunicationTeam Work

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