Bristol Myers Squibb (BMS) has announced an opening for the position of Scientific Writer II in Hyderabad, Telangana. The role is focused on the preparation, coordination and review of regulatory and clinical development documents.
Candidates with a PharmD, PhD, Master’s or Bachelor’s degree in a relevant scientific discipline may be eligible, depending on their relevant regulatory documentation experience. Candidates with approximately 2 to 4 years of experience in regulatory documentation are specifically mentioned in the job requirements.
Interested candidates can check the complete details below and apply through the official BMS careers portal.
BMS Scientific Writer II Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company | Bristol Myers Squibb |
| Job Title | Scientific Writer II |
| Job Requisition ID | R1606692 |
| Job Location | Hyderabad, Telangana |
| Employment Type | Full Time |
| Experience | Approximately 2–4 years in regulatory documentation |
| Qualification | PharmD / PhD / Master’s / Bachelor’s in relevant scientific discipline |
| Job Category | Scientific / Regulatory Writing |
| Application Mode | Online |
BMS Scientific Writer II Eligibility
Candidates applying for the Scientific Writer II position should have an appropriate scientific or pharmaceutical educational background along with relevant regulatory documentation experience.
Educational Qualification
Candidates with any of the following backgrounds may be considered:
- PharmD
- PhD in a relevant scientific discipline
- Master’s degree in a relevant scientific discipline
- Bachelor’s degree in a relevant scientific discipline
The job description specifically states that PhD candidates in biological sciences and PharmD candidates are considered.
Experience
Candidates with approximately 2 to 4 years of experience in regulatory documentation are mentioned in the qualification requirements.
Relevant experience may include authoring and managing regulatory and clinical development documents such as:
- Investigator’s Brochures (IB)
- Safety Aggregate Reports
- Clinical Study Reports (CSR)
- Clinical Protocols
- Other regulatory documentation
Key Responsibilities
The selected candidate will support the preparation and management of important scientific and regulatory documents throughout the drug development process.
Key responsibilities include:
- Coordinate and author regulatory documents such as Investigator’s Brochures, Development Safety Update Reports, Periodic Benefit-Risk Evaluation Reports, Clinical Study Reports and protocols.
- Coordinate scientific, medical and regulatory input received from development team members.
- Participate in document subteams and help manage timelines for assigned documents.
- Contribute to document strategy discussions involving messaging, document flow, logic and consistency.
- Maintain document prototypes and document shells.
- Coordinate the review process in accordance with applicable internal and external procedures.
- Identify and resolve document-related issues, errors and inconsistencies in collaboration with relevant team members.
- Review and edit scientific and regulatory documents when required.
- Help ensure assigned documents are completed on time and meet expected quality standards.
Required Skills
Candidates should have strong scientific writing and document management abilities.
Important skills include:
- Strong scientific and regulatory writing skills.
- Experience authoring or managing regulatory documentation.
- Ability to analyze and interpret complex scientific information.
- Understanding of global pharmaceutical drug development.
- Good organizational and time-management skills.
- Strong written and verbal communication.
- Ability to work effectively with cross-functional teams.
- Facilitation and stakeholder coordination skills.
- Working knowledge of document management systems.
- Basic understanding of the document publishing process.
- Strong attention to document quality, consistency and timelines.
Regulatory Documents Experience
Experience with documents such as the following can be relevant to this role:
- Investigator’s Brochures (IB)
- Safety Aggregate Reports
- Clinical Study Reports (CSR)
- Clinical Protocols
- Development Safety Update Reports
- Periodic Benefit-Risk Evaluation Reports
The ability to coordinate scientific, medical and regulatory contributions is an important part of the position.
About Bristol Myers Squibb
Bristol Myers Squibb (BMS) is a global biopharmaceutical company focused on discovering, developing and delivering medicines for serious diseases.
The company describes its work environment as purpose-driven and emphasizes collaboration, inclusion, employee development and patient impact.
BMS Scientific Writer II Recruitment 2026 – Application Process
Eligible and interested candidates can apply online through the official Bristol Myers Squibb careers portal.
Job Details
Job Title: Scientific Writer II
Job Location: Hyderabad, Telangana
Job Type: Full Time
Job Requisition ID: R1606692
Candidates should review the complete eligibility requirements before submitting their application.
Official Apply: BMS Careers – Scientific Writer II
Important Points
- The position is based in Hyderabad, Telangana.
- This is a full-time opportunity.
- Relevant experience in regulatory documentation is required.
- PharmD and relevant PhD candidates are specifically considered.
- Candidates should have strong scientific writing and document management skills.
- Experience with regulatory and clinical documents is relevant to the position.
- The job description does not provide a salary or CTC figure.
- BMS states that candidates are evaluated based on skills and capabilities and encourages interested applicants to apply even if their profile does not perfectly match every listed requirement.
Frequently Asked Questions
What is the position offered by BMS?
Bristol Myers Squibb is hiring for the position of Scientific Writer II.
Where is the Scientific Writer II job located?
The position is based in Hyderabad, Telangana, India.
What is the job requisition number?
The BMS job requisition number is R1606692.
What qualification is required?
Candidates with a PharmD, PhD, Master’s or Bachelor’s degree in a relevant scientific discipline may be considered, depending on their relevant experience.
How much experience is required?
The job description mentions approximately 2 to 4 years of regulatory documentation experience.
What type of documents will the candidate work on?
The role involves regulatory and clinical development documents, including Investigator’s Brochures, safety reports, clinical protocols and Clinical Study Reports.
Is salary information available?
No salary or CTC information is provided in the supplied job description.
How can candidates apply?
Interested candidates can submit their application through the official Bristol Myers Squibb careers portal using the job requisition ID R1606692.
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