Bristol Myers Squibb Require Safety Data Sheet Specialist Writer

Bristol Myers Squibb (BMS) is a major global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases, particularly in areas like oncology, immunology, hematology, and cardiovascular conditions, with key products including Opdivo, Eliquis, and Revlimid, aiming to transform patient lives through science. Headquartered in Princeton, New Jersey, BMS has a significant global presence and invests heavily in research and development to address unmet medical needs.

Post : Specialist - Safety Data Sheet Writer

Job Description
• Collect, compile and document toxicological, physical, environmental, and other scientific data, as well as regulatory information, related to BMS materials for the creation of SDSs.
• Interpret chemical data and classify hazards based on GHS and other regional frameworks (e.g., EU CLP).
• Ensure compliance with international regulations regarding SDSs (e.g., OSHA HazCom, EU CLP, REACH).
• Collaborate with cross-functional teams following formulation changes, regulatory updates or new hazard information.
• Design and/or improve internal chemical stewardship processes to enhance agility and minimize business risk.
• Perform dangerous goods (DG) classifications.
• Participate in quality control reviews to ensure accuracy and completeness of data used in SDS authoring.
• Help maintain and update internal databases/repositories for chemical hazard and regulatory information.
• Contribute to streamlining the SDS workflow, reducing turnaround time, and enhancing data collection processes.
• Support creation of training content or guidance documents for internal teams regarding SDS requirements and hazard communication.

Candidate Profile
• Bachelor's degree in chemistry, toxicology, product stewardship, industrial hygiene or related discipline required.
• Advanced degree is a plus.
• 3+ years in SDS authoring and/or regulatory compliance in chemical, pharmaceutical, or manufacturing industries.
• Proficiency with SDS authoring software required (e.g., SAP EHS module, WERCS, 3E).
• Familiarity with GHS, OSHA HazCom, EU CLP and/or other global chemical regulations.
• • Certification in DG regulations (DOT, IATA, IMDG) is desirable.
• Lean Six Sigma or similar certifications are not required but considered a plus.
• Exposure to project management principles or experience working in cross-functional teams is beneficial.
• Strong communication and interpersonal skills; Excellent attention to detail and organizational skills are a must; acts with integrity.
• Ability to innovate. Strives to enhance performance by doing things that are unique and leading edge; experience with AI and/or process automation is a plus. Willingly embraces changes needed to adapt to new circumstances and uncertainties.

Additional Information
Experience : 3+ years
Qualification : Bachelor's degree
Location : Hyderabad - TS - IN
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Safety Data
End Date : 10th February 2026