Work as Associate Regulatory Specialist at Solenis

A Solenis Company, our commitment to Diversity, Equity, and Inclusion (DE&I) is not just a philosophy but a fundamental part of our organizational DNA. Diversey India has once again been recognized as one of the "100 Best Companies for Women in India 2023" by AVTAR & SERAMOUNT Group. This prestigious acknowledgment reflects our sustained dedication to cultivating a workplace that champions gender inclusivity.

Post : Associate Regulatory Specialist

Job Description
• Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard communication regulations.
• Derive hazard classifications for substances and mixtures using various classification regulations including but not limited to GHS, CLP, & OSHA Hazard Communication Standard.
• Perform raw material compliance, formula and finished products reviews for various regions as per the Globally Harmonized System (GHS).
• Maintain data integrity within the SDS authoring software & ERP System to ensure that Safety Data Sheets & information reflect the most current health, safety, environmental, and regulatory information available.
• Efficiently address queries from internal/external stakeholders & coordinate with team lead/ SME’s if required, for quick resolution for high priority requests.
• Prioritize & complete requests based on defined turnaround time.
• Ensure records are maintained as per defined formats.

Candidate Profile
• Good knowledge of global chemical regulatory environment and applicable legislations / guidelines
• Working experience in a corporate regulatory environment with a proven track record of interaction with competent authorities in carrying out the responsibilities of product registration, regulatory compliance, regulatory consulting or equivalent
• Knowledge of hazard communication as per GHS and country specific requirements, hands-on experience on label and SDS authoring
• Demonstrated success in completion of difficult tasks in a timely manner
• Good communication, presentation, and analytical skills.
• Desirable to have knowledge of regulatory terminology and regulatory landscape.
• Ability to work effectively with a cross functional team and independently with minimal supervision
• Excellent communication in English, verbal and writing.

Additional Information
Job ID : R0014389
Qualification : M.Pharm, B.Pharm, M.Sc
Location : Mumbai, India
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 31st August 2024