Dr. Reddy’s Medical Writer Opportunity

Medical Writer Opportunity at Dr. Reddy’s – Hyderabad | M.Pharm Graduates with 3–6 Years Experience Preferred

Looking for a dynamic role in clinical development writing? Apply for the Medical Writer position at Dr. Reddy’s Laboratories in Hyderabad. This hybrid role is ideal for M.Pharm graduates with 3–6 years of experience in QC and formatting of clinical documents.

Medical Writer – M.Pharm Clinical Writing Job in Hyderabad

Apply now for Medical Writer job at Dr. Reddy’s in Hyderabad. M.Pharm with 3–6 yrs exp in QC & clinical documentation preferred. Hybrid work mode.

Career with Dr. Reddy’s as a Medical Writer – Hyderabad

Dr. Reddy’s Laboratories Ltd., a renowned name in global pharmaceutical innovation, invites applications for the Medical Writer role within the Clinical Development department. Based in Hyderabad, this hybrid full-time opportunity is a strategic fit for experienced professionals in clinical research documentation and quality control.

This role is part of the company’s fast-growing Biologics division, contributing directly to high-impact biosimilar development programs.

About Dr. Reddy’s Laboratories

Founded in 1984, Dr. Reddy’s has grown from a small Indian firm into a global pharmaceutical leader with a presence in 66 countries, over 24,000 employees, and a focus on affordable and innovative healthcare.

With robust R&D, end-to-end product development, and a strong commitment to sustainability and equality, the company aims to reach 1.5 billion+ patients globally by 2030. Dr. Reddy’s fosters a diverse and inclusive workplace, empowering professionals to thrive.

Key Responsibilities

Document Quality Control & Formatting

• Perform QC and formatting of clinical trial protocols, ICFs, CSRs, IBs, and clinical data summaries across all trial phases
• Ensure accuracy and compliance in eCTD dossier clinical modules for global regulatory submission

Ad-hoc Writing and Support

• Support document writing (ICFs, CSRs, protocols) on request
• Assist Medical Affairs and Clinical Development teams with QC and formatting
• CSR publishing and SOP/checklist/template development

Collaboration & Oversight

• Collaborate with cross-functional stakeholders within Clinical Development
• Maintain and track occupancy/resourcing in coordination with the Group Lead

Required Qualifications

• Educational Background: M.Pharm in Pharmaceutical Sciences or related discipline
• Experience: 3–6 years in QC, formatting, or medical writing in the pharmaceutical/clinical domain
• Proficiency in Microsoft Office, Adobe Acrobat, and document publishing tools
• Understanding of clinical trials, medical terminology, and regulatory writing standards
• Excellent communication, attention to detail, and time management skills

Preferred Skills

• Experience in regulatory writing and eCTD document submission
• Prior role as Medical Writer, QC Specialist, or in Clinical Operations support

Location & Work Environment

• Location: Hyderabad, Telangana
• Work Mode: Hybrid (on-site & remote flexibility)
• Business Unit: Biologics (Global Biosimilars Division)

Perks & Benefits

• Competitive compensation and relocation assistance
• Comprehensive health and life insurance for self and family
• Learning and development programs
• Maternity & paternity leave benefits

Dr. Reddy’s nurtures a culture of innovation, empathy, and integrity, making it a desirable destination for skilled pharma professionals.

Call to Action

Interested candidates can apply directly on the Dr. Reddy’s career portal:
Apply Here

Ensure your resume highlights relevant experience in clinical writing and document quality control.

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