Job Title: Specialist – Safety Data Sheet (SDS) Writer
Location: Hyderabad, Telangana, India
Job Type: Full-Time
Experience Required: Minimum 3 years in SDS authoring or regulatory compliance
Company Overview:
Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to transforming patients’ lives through science. At BMS, every role contributes to meaningful, life-changing work—from advancing cutting-edge therapies to enhancing operational excellence. Our inclusive culture fosters innovation, collaboration, and career growth while promoting work-life balance and professional development.
Role Overview:
We are seeking a Specialist – Safety Data Sheet Writer to collect, compile, and document chemical, toxicological, physical, environmental, and regulatory data for BMS materials. This role ensures the accurate preparation of SDSs compliant with global standards and contributes to improving internal processes, reducing risk, and enhancing efficiency in chemical stewardship.
Key Responsibilities:
Author and maintain Safety Data Sheets (SDSs) in compliance with international regulations (GHS, OSHA HazCom, EU CLP, REACH).
Collect, interpret, and classify chemical hazards using toxicological, environmental, and physical data.
Collaborate with cross-functional teams to update SDSs following formulation changes, new hazard data, or regulatory updates.
Perform Dangerous Goods (DG) classification and maintain regulatory compliance.
Conduct quality control reviews to ensure SDS accuracy and completeness.
Maintain and update internal chemical and regulatory information databases.
Streamline SDS workflows to enhance efficiency, reduce turnaround times, and improve data collection processes.
Support the creation of guidance and training materials for internal stakeholders on SDS and hazard communication.
Contribute to continuous improvement initiatives leveraging AI or automation tools where applicable.
Required Qualifications:
Bachelor’s degree in Chemistry, Toxicology, Product Stewardship, Industrial Hygiene, or related discipline (Advanced degree preferred).
Minimum 3 years of experience in SDS authoring, chemical safety, or regulatory compliance within pharmaceutical, chemical, or manufacturing industries.
Proficiency in SDS authoring software (SAP EHS, WERCS, 3E, or equivalent).
Knowledge of global chemical regulations (GHS, OSHA HazCom, EU CLP, REACH).
Strong analytical, organizational, and communication skills with high attention to detail.
Demonstrated ability to work in cross-functional teams and manage multiple priorities.
Certification in DG regulations (DOT, IATA, IMDG) and Lean Six Sigma is a plus.
Innovative mindset with the ability to adapt to regulatory changes and evolving business needs.
Why Join BMS:
Be part of a global company with a mission to transform patients’ lives through science.
Work on challenging and impactful projects with high-achieving teams.
Access to comprehensive benefits, learning opportunities, and career development programs.
Flexible and supportive work environment with hybrid options for eligible roles.
Inclusive culture emphasizing collaboration, integrity, and diversity.
Equal Opportunity Statement:
Bristol Myers Squibb is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, religion, sexual orientation, gender identity, disability, veteran status, or any other protected characteristic under applicable law.
Apply Now to contribute to life-changing work in regulatory compliance and chemical safety at BMS.
Learn more about BMS careers: careers.bms.com
Job ID: R1597654
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