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Maithri Drugs Hiring In Regulatory Affairs

Published on

Maithri Drugs

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

25,000 - 35,000 /month

Hyderabad

1 to 2 Years

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This is a full-time on-site role for a Regulatory Affairs Executive located in Hyderabad. The Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs.

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Responsibilities

  • Regulatory Documentation: Assist in the preparation, compilation, and maintenance of regulatory documentation.
  • Compliance: Ensure that all products comply with regulatory requirements.
  • Dossier Preparation: Prepare and manage regulatory dossiers for submission.
  • Regulatory Affairs Management: Oversee and manage regulatory affairs processes.

Qualifications

  • Experience:
    • Regulatory documentation
    • Regulatory requirements
    • Regulatory compliance
  • Skills:
    • Proficiency in dossier preparation
    • Knowledge of regulatory affairs
    • Excellent attention to detail and organizational skills
    • Strong problem-solving and analytical skills
    • Good communication and interpersonal skills
    • Ability to work effectively in a team

Application Link

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PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.

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