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  • Bristol Myers Squibb (BMS) Hiring SDS Specialist Writers in Hyderabad: Transforming Patient Lives Through Science
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Bristol Myers Squibb (BMS) Hiring SDS Specialist Writers in Hyderabad: Transforming Patient Lives Through Science

Pharm'Up 2 min read

Bristol Myers Squibb (BMS), a premier global biopharmaceutical leader known for its groundbreaking work in oncology and immunology, has announced an opening for a Specialist – Safety Data Sheet (SDS) Writer at its Hyderabad facility. This role is central to the company’s mission of ensuring the highest safety standards for its innovative medical solutions, including global brands like Opdivo and Eliquis.

The position offers a unique opportunity for scientific professionals to bridge the gap between complex toxicological data and international regulatory compliance, contributing directly to global chemical stewardship and patient safety.

Key Responsibilities & Impact

The SDS Specialist Writer will be responsible for the end-to-end authoring and management of safety documentation. Primary duties include:

  • Data Synthesis: Collecting and documenting toxicological, physical, and environmental scientific data for BMS materials.
  • Regulatory Interpretation: Classifying chemical hazards based on GHS and regional frameworks like EU CLP and OSHA HazCom.
  • Cross-Functional Collaboration: Partnering with internal teams to update safety data following formulation changes or new regulatory insights.
  • Operational Excellence: Performing Dangerous Goods (DG) classifications and utilizing Lean Six Sigma principles to streamline the SDS workflow and reduce turnaround times.
  • Innovation: Implementing process automation and potentially AI-driven tools to enhance data collection and business agility.

Candidate Profile

BMS is looking for detail-oriented professionals with a strong scientific background:

  • Education: Bachelor’s degree in Chemistry, Toxicology, Product Stewardship, or Industrial Hygiene (Advanced degrees preferred).
  • Experience: 3+ years in SDS authoring or regulatory compliance within the Pharma or Chemical manufacturing sectors.
  • Software Proficiency: Mandatory experience with SDS authoring software such as SAP EHS module, WERCS, or 3E.
  • Certifications: While not mandatory, certifications in DG regulations (DOT, IATA, IMDG) or Lean Six Sigma are highly desirable.

Job Details at a Glance

  • Location: Hyderabad, Telangana, India
  • Experience Level: 3+ Years
  • Industry: Pharma / Biopharma / Clinical Research
  • Application Deadline: February 10, 2026

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