Medical Regulatory Writer Jobs for Life Science, Pharma Graduates – Sanofi Hyderabad

Medical Regulatory Writer Jobs for Life Science, Pharma Graduates – Sanofi Hyderabad

Apply now for Medical Regulatory Writer roles at Sanofi in Hyderabad. Openings for PhD, MPharma, BPharma, MBBS, BHMS, BDS with 2+ years experience.

Medical Regulatory Writer Jobs at Sanofi – Apply in Hyderabad Today!

If you’re a science graduate looking to work with a global pharmaceutical giant, here’s your opportunity! Sanofi is hiring Medical Regulatory Writers for its Hyderabad location. Whether you hold a PhD, MSc, BPharma, MPharma, MBBS, BDS, BHMS, or BAMS, and have 2+ years of regulatory writing experience, this role opens the door to a promising career in medical regulatory writing with one of the top players in healthcare.

About Sanofi Business Operations

Sanofi Business Operations in India serves as a strategic hub, supporting multiple global verticals—Specialty Care, General Medicines, Vaccines, R&D, and more. This division functions as the backbone for delivering high-quality, compliant content and communications to Sanofi’s global teams.

Job Overview

Position: Medical Regulatory Writer

Location: Hyderabad, India

Job Type: Permanent, Full-Time

Department: Scientific Communications

Reporting To: Head Scientific Communications / Team Lead

Key Responsibilities

Core Medical Writing Tasks

• Author and edit high-quality safety and medical documents.
• Deliver materials such as:
  • Periodic Benefit-Risk Evaluation Reports (PBRERs)
  • Addendum to Clinical Overview (ACO)
  • Disease/Product ID Cards
  • Product Alerts
  • Trial Transparency Documents
• Maintain compliance with internal/external writing standards.

Strategic Collaboration

• Partner with global scientific, regulatory, and pharmacovigilance teams.
• Contribute to strategic planning and execution of medical writing needs.
• Support content development for trial registry submissions (CTG, EUCTR, EUDRACT).

Stakeholder Engagement

• Engage with global stakeholders in clinical, medical, legal, and corporate affairs teams.
• Maintain audit-readiness and manage documentation systems.

 Continuous Improvement

• Monitor feedback and continuously enhance writing quality.
• Stay updated on Sanofi’s evolving quality and policy documents.

Eligibility Criteria

Required Education

• PhD, MPharma, BPharma
• MSc in Life Sciences
• MBBS, BDS, BHMS, BAMS
• DPharm, PharmD

Required Experience

• Minimum 2 years in regulatory writing in pharma or healthcare.

Technical & Soft Skills

• Proficient in ICH/GCP/GVP guidelines.
• Strong command of medical terminology and scientific literature.
• Excellent communication, stakeholder, and time-management skills.
• Fluent in English.

Call to Action

Ready to elevate your career in regulatory medical writing? Apply now and become a part of Sanofi’s mission to deliver better science and better healthcare outcomes globally.

Apply Now on Sanofi Careers

 Quick Summary Table

Company Name	Current Vacancies in Departments	Required Education	Experience Required
Sanofi	Medical Regulatory Writing	PhD, MPharma, BPharma, MBBS, BDS, BHMS, MSc, DPharm, PharmD	Minimum 2 years