Scientific Writer II Position at Bristol Myers Squibb in Hyderabad

A rare opportunity in BMS careers has emerged for aspiring scientific writers at Bristol Myers Squibb in Hyderabad. The organization seeks candidates with 2 to 4 years of experience in regulatory documentation, specifically those with a PharmD, PhD, or relevant life sciences background. Applications are currently open for this exciting opportunity.

About Bristol Myers Squibb

Bristol Myers Squibb (BMS) is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. With a commitment to scientific excellence and patient care, BMS operates in various therapeutic areas, including oncology, immunology, cardiovascular disease, and fibrosis. The company is headquartered in New York City, USA, and maintains a strong presence in India.

Company: Bristol Myers Squibb

Location: Hyderabad, Telangana, India

Job Type: Full Time

Job Requisition: R1606692

Experience: ~2–4 years in regulatory documentation

Qualification: PharmD / PhD / life sciences (Master’s with ~2–4 years in regulatory documentation)

Posted On: 24 September 2026

BMS Careers: Job Description

For professionals exploring BMS careers, the Scientific Writer II role focuses on preparing and coordinating important regulatory and clinical development documents. The position involves working with scientific, medical, and regulatory stakeholders to produce accurate, consistent, and high-quality documentation. This opportunity may be particularly relevant for PharmD, PhD, and life-science professionals interested in regulatory medical writing and clinical documentation.

Key Responsibilities

• Coordinating and authoring regulatory documents.
• Preparing documents such as Investigator’s Brochures (IBs), Development Safety Update Reports (DSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Clinical Study Reports (CSRs), and clinical protocols.
• Coordinating scientific, medical, and regulatory input from development teams.
• Participating in document subteams.
• Planning and managing document timelines.
• Participating in document strategy meetings.
• Contributing to messaging, document flow, logic, and consistency.
• Managing review processes according to internal and external guidelines.

Eligibility Criteria

• PharmD or PhD in a relevant scientific discipline; or
• Bachelor’s or Master’s degree with approximately 2–4 years of regulatory documentation experience.
• Strong scientific writing skills.
• Experience authoring or managing regulatory documents such as IBs, safety aggregate reports, clinical protocols, and/or CSRs.
• Ability to analyze and interpret complex scientific data.
• Understanding of global pharmaceutical drug development.
• Strong organizational and communication skills.
• Working knowledge of document management systems.

How to Apply

Interested candidates can apply through the official application link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

This opportunity within BMS careers is an excellent chance for qualified candidates to join Bristol Myers Squibb as a Scientific Writer II in Hyderabad. Interested individuals are encouraged to apply before the deadline to take the next step in their careers in the pharmaceutical industry.