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• Collect, compile, and document toxicological, physical, environmental, and regulatory data required for authoring Safety Data Sheets (SDSs) for BMS materials.
• Interpret chemical and toxicological data to classify hazards in accordance with GHS and other regional regulatory frameworks (e.g., EU CLP).
• Ensure SDS compliance with global regulations including OSHA Hazard Communication, EU CLP, and REACH requirements.
• Perform Dangerous Goods (DG) classifications in line with applicable regulations (DOT, IATA, IMDG).
• Collaborate with cross-functional teams to manage formulation changes, regulatory updates, and new hazard information.
• Participate in quality control and peer review processes to ensure accuracy, consistency, and completeness of SDS content.
• Maintain and update internal databases and repositories for chemical hazard and regulatory information.
• Design, improve, and streamline internal chemical stewardship and SDS authoring workflows to reduce turnaround time and minimize business risk.
• Support the development of internal training materials and guidance documents related to SDS requirements and hazard communication.
• Contribute to process improvement initiatives, including automation, AI-driven solutions, and continuous improvement efforts.
• Bachelor’s degree in Chemistry, Toxicology, Product Stewardship, Industrial Hygiene, or a related scientific discipline.
• Advanced degree is preferred but not mandatory.
• Minimum of 3 years’ experience in SDS authoring and/or regulatory compliance within chemical, pharmaceutical, or manufacturing industries.
• Hands-on experience with SDS authoring software such as SAP EHS, WERCS, 3E, or equivalent platforms.
• Exposure to project management and cross-functional collaboration is beneficial.
• Strong knowledge of global chemical regulations including GHS, OSHA HazCom, EU CLP, and REACH.
• Proficiency in hazard classification, toxicological data interpretation, and regulatory documentation.
• Certification in Dangerous Goods regulations (DOT, IATA, IMDG) is desirable.
• Excellent attention to detail with strong organisational and documentation skills.
• Strong communication and interpersonal skills with the ability to work effectively in cross-functional teams.
• Ability to innovate, adapt to change, and enhance performance through process improvement and automation initiatives.
• High level of integrity, accountability, and commitment to quality and compliance.
• Bristol Myers Squibb (BMS) is a global biopharmaceutical company committed to transforming patients’ lives through science.
• BMS delivers innovative medicines in areas such as oncology, immunology, cardiovascular disease, and cell therapy.