Regulatory Affairs

🔹 Job Title:

🏢 Company:

📍 Location:

🧾 Vacancies:

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🧪 Department:

About Cian Healthcare Ltd.

WHO-GMP & ISO-certified pharmaceutical company

quality, innovation, and compliance

Key Responsibilities

• Preparation, review, and compilation of

  CTD/eCTD dossiers

  for product registration in domestic and international markets.
• Coordinate with

  R&D, QA, QC, Production, and Packaging

  teams for documentation and data collection.
• Prepare

  Module 1–5

  as per country-specific regulatory guidelines.
• Handle

  regulatory submissions, renewals, and variations

  in coordination with global partners.
• Maintain and update

  product registration databases

  and submission trackers.
• Review

  labeling, artwork, and promotional material

  for compliance.
• Support in responding to

  regulatory queries and deficiency letters

  .
• Ensure compliance with

  regulatory updates and global guidelines

  (ICH, USFDA, EMA, MHRA, WHO, etc.).

Required Skills & Qualifications

• B.Pharm / M.Pharm / M.Sc.

  (Chemistry, Biotechnology, or related field).
• Minimum

  1 year of hands-on experience

  in dossier preparation (

  CTD/eCTD format

  ).
• Good understanding of

  international regulatory guidelines

  .
• Strong

  documentation, analytical, and communication skills

  .
• Proficiency in

  MS Office

  and

  eCTD compilation software

  will be an added advantage.

Work Location

Cian Healthcare Ltd.

Pune, Maharashtra

Employment Type:

How to Apply

Interested candidates can share their updated resumes at:

hrd@cian.co

ramanager@cian.co

suraj@cian.co

Vaishali: