Manager, Central Monitor, Data Surveillance, Clinical Data Sciences

Roles & Responsibilities

• Create and maintain Safety Data Sheets (SDS) for global markets
• Perform hazard classification as per GHS, CLP, OSHA regulations
• Handle regulatory compliance workflows including labels, registrations, renewals
• Review raw materials, formulations, and finished products for compliance
• Maintain regulatory data accuracy in SDS authoring tools and ERP systems
• Respond to regulatory queries from internal and external stakeholders
• Ensure documentation and records meet regulatory standards and timelines

Qualification

• Bachelor’s or Master’s degree in Chemistry, Pharmacy, Chemical Engineering, or related field

Experience

• Experience in corporate regulatory affairs or chemical regulatory environment
• Hands-on exposure to SDS and label authoring
• Experience in product registration or regulatory compliance preferred

Skills

• Strong knowledge of global chemical regulations (GHS, CLP, OSHA)
• SDS and label authoring experience
• Good analytical, documentation, and communication skills
• Ability to work independently and with cross-functional teams

About the Organisation

Diversey, a Solenis company, is a global leader in hygiene and cleaning solutions. Its Global Regulatory Affairs Service Center (GRASC) in Mumbai supports worldwide regulatory compliance across Diversey’s chemical product portfolio, offering strong global exposure and professional growth.