Safety Data Sheet Writer - New Brunswick, United States - SSi People

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    Description

    Roles & Responsibilities:

    • Collect, compile, evaluate and document toxicological, physical, pharmacological, , investigator brochures, clinical study reports, environmental, and other scientific data, as well as regulatory information, related to BMS materials.
    • Perform routine categorizations and calculations.
    • Prepare toxicological classification forms for materials with 5-pack studies (eye, skin, respiration, sensitization and mutagenicity) in regulation with US, Europe and Globally Harmonized jurisdictions.
      • Author Safety Data Sheets using BMS software in SAP.
    • Complete and revise SDS requests within established timelines
    • Regular communication with toxicologists, Scientists and Chemists for supporting documents for Safety Data Sheets.
    • Maintain material documentation files.
    • Perform physical classification of materials based off chemical structures as part of the classification process.
    • Work collaboratively with various organizations including but not limited to R&D, Marketing, Product Management to produce required documentation in a timely manner for key stake holders.

    Knowledge & Skills

    • Working knowledge of Global Harmonized System (GHS)
    • The ability to learn technical processes quickly.
    • Ability to effectively communicate with wide variety of stakeholders.
    • Demonstrated computer skills and proficiency using Microsoft tools: SharePoint, access, excel, outlook.
    • Ability to take initiative and adapt to frequently changing priorities simultaneously and think creatively, critically, and strategically to solve problems in a complex environment with urgency, agility, and calm.

    Education & Experience:

    • Bachelor's degree or higher in EHS, Toxicology, Industrial Hygiene, Chemistry, Engineering, or other science discipline.
    • At least of 1- 2 year of related experience authoring SDS's required. Experience using SAP to author SDS is a plus.
    • Regulatory affairs/Product stewardship experience.