Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions.
Post : Safety Data Sheets Expert
Job Description
• Provision of strategic advice to the businesses with regards to regulatory compliance linked to substances including biological products, infectious agents etc (e.g. safety data sheets, classification, packaging & labelling, transport classification, local regulations). This includes monitoring of regulations.
• Act with efficiency with the Global Product Stewardship team.
• Edit and maintain Safety Data Sheets using our IT tools.
• Independent evaluation and validation of substance data for classification and labelling according to international regulations e.g., GHS/CLP, Seveso, and transport regulations.
• Documents all product stewardship information including references, reports to track and to justify any modification in the versioning of the documents used by Product Stewardship (SDSs, Hazard Classification Sheets & data).
• Conducting substance data searches and evaluating the results. Collecting, documenting and providing data in internal substance databases.
• Communicating effectively in written and oral ways, results and conclusions with contacts of sites and business units.
Candidate Profile
• Education : Bachelor’s degree in Biological Science (biology, microbiology, Molecular Biology) or technical discipline at minimum.
• Languages : Good coordination and communication skills.
• Experience : 5+ years of industry experience including 2+ years' experience in Product Stewardship.
• Soft skills : Be able to work effectively in a team and on your own initiative. Self-starter with the ability to perform under rapidly evolving contexts. Data-based decision maker and methodical in the analysis. Ability to provide clear concise explanations. Able to work independently, team player and networker. Important sense for transversal impact. Ability to communicate effectively, orally and in writing. Knowledge in biologicals is required not a plus
Technical skills : Professional experience in the field of product safety/product stewardship, chemical / biological laws, classification and labelling of hazardous substances. Experience in writing and reading Material Safety Data sheets. SDS-Writing - Certified competent person according to §18 (4) Hazard Substance Ordinance (Germany) Ability to rank relative compliance risks, high sense of responsibility and compliance and prioritize resulting actions. Ability to keep abreast of compliance changes. Strong proficiency in common chemical regulations. Have critical thinking, problem solving & planning skills. Proficiency in SAP-EHS module is needed. Proven experience of interactions of SAP-EHS with SAP based ERP is needed.
• Proven experience of SERC – SAP EHS Regulatory Content (now 3E ERC EHS Regulatory Content) is needed. Certified IATA training for Dangerous Goods Transportation is needed. Proven knowledge on toxicological / pharma toxicological backgrounds would be a plus. Knowledge in the use of Artificial Intelligence for the use of designing SDSs would be a plus(e.g. tool from Opesus). Experience on Extended SDS would be a plus. Knowledge on Biocides and Biological agents
Additional Information
Experience : 2+ years
Qualification : Bachelor’s degree in Biological Science (biology, microbiology, Molecular Biology)
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : Oct. 23, 2026
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