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Sanofi Hiring for Medical Regulatory Writer

Join Sanofi Business Operations and make an impact in the pharmaceutical industry as a Medical Regulatory Writer. Contribute to high-quality regulatory documentation while supporting global business units, including Specialty Care, Vaccines, General Medicines, and more. Sanofi Hiring for Medical Regulatory Writer


Job Details

  • Position: Medical Regulatory Writer
  • Location: Hyderabad
  • Experience: Minimum 2 years in regulatory writing
  • Salary: ₹6 – ₹12.5 LPA
  • Qualifications:
    • Required: PhD, B.Sc, M.Sc, M.Pharm, Pharm.D, B.Pharm, MBBS, BDS, BAMS, BHMS, or MD

About Sanofi Business Operations

Sanofi Business Operations is a strategic organization that provides centralized services to enhance Medical, HEVA, and Commercial operations globally. It supports various divisions, including R&D, Vaccines, Data & Digital functions, and more, focusing on innovation and quality. Sanofi Hiring for Medical Regulatory Writer


Main Responsibilities

As a Medical Regulatory Writer, your responsibilities include:

Document Development

  • Author and edit medical sections for:
    • Periodic Benefit-Risk Evaluation Reports (PBRER)
    • Addendums to clinical overviews
    • Disease and Product ID Cards
    • Product alerts and trial transparency documents
  • Deliver high-quality, compliant regulatory content.

Collaboration

  • Work with Scientific Communication, Medical Regulatory Writing, Pharmacovigilance, and Regulatory Affairs teams.
  • Build strong relationships with stakeholders within allocated business units and product areas.
Sanofi Hiring for Medical Regulatory Writer
Sanofi Hiring for Medical Regulatory Writer

Content and Process Management

  • Post and track documents on platforms like CTG, EUCTR, and EUDRACT.
  • Support the implementation of annual medical regulatory plans.
  • Ensure audit-readiness and compliance with Sanofi quality standards.

Expertise Development

  • Gain deep knowledge of Therapeutic Areas (TAs).
  • Participate in planning data analyses and presentations under guidance.

Skills and Qualifications

Experience

  • Over 2 years of regulatory writing experience in the pharmaceutical or healthcare industry.
See also  Sudeep Nutrition Hiring for Regulatory Affairs Executive – Walk-In Interview

Technical Skills

  • Proficiency in medical writing, editing, and summarizing scientific information.
  • Knowledge of ICH guidelines, GCP/GVP, and regulatory requirements.
  • Skills in data retrieval, scientific interpretation, and medical literature screening.

Soft Skills

  • Strong stakeholder and vendor management abilities.
  • Excellent communication skills, both verbal and written.
  • Ability to work independently and as part of a team.

Education

  • Advanced degrees in Life Sciences, Pharmacy, or related fields (e.g., PhD, M.Pharm, M.Sc).
  • Medical degrees like MBBS, BDS, BAMS, BHMS, or MD are also eligible.

Language Proficiency

  • Fluent in English (reading, writing, and speaking).

Why Join Sanofi?

Sanofi values work-life balance, flexibility, and career growth. This role offers an opportunity to contribute to global healthcare outcomes while working with cutting-edge regulatory processes.

Apply online now and become a part of a world-class organization dedicated to innovation and quality! Sanofi Hiring for Medical Regulatory Writer

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Sanofi Hiring for Medical Regulatory Writer
Sanofi Hiring for Medical Regulatory Writer
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