• Regulatory Affairs Director

    Actalent (Bowling Green, OH)


    Regulatory Affairs Director

     

    INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM

     

    OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823

    Job Description

    As a Regulatory Affairs Director, you will develop, implement, and coordinate compliance with federal, state, local, and international regulatory requirements applicable to institution cleaning chemicals, equipment, water-based coatings, and bacillus species. You will be responsible for providing analysis and support for the company’s compliance activities, managing day-to-day administration of regulatory matters, and promoting sound product stewardship. This role requires providing technical advice concerning regulatory affairs to internal team members and customers, as well as organizing and maintaining proper documentation regarding regulatory compliance.

    Responsibilities

    + Proof all labels for chemical and equipment, Basic Coatings, and Bio-Systems, including accompanying literature, training materials, or other written or digital materials for compliance with OSHA, FIFRA, CPSC, OAQPS, FDA, DOT, EPA, USDA, CDC, VOC, and other applicable federal, state, or local requirements.

    + Ensure accuracy of warning statements and first aid statements on labels, and compliance on labels and (M)SDS’s according to US and International requirements.

    + Monitor activities at federal, state, and regional regulatory agencies to find opportunities for new product development and present findings.

    + Analyze, interpret, and present information to senior management concerning regulatory affairs related to current and potential future products.

    + Lead the implementation of regulatory requirements to ensure compliance.

    + Maintain and ensure accuracy of OSHA SDS generation Sphera, raw material SDS database, and assignment of proper BOL codes to products.

    + Ensure communication and compliance with OSHA, FIFRA, CPSC, OAQPS, FDA, DOT, EPA, USDA, CDC, VOC, and other applicable federal, state, or regional requirements.

    + Handle DOT UN approved container testing, NAFTA classification of chemicals and equipment parts, EU REACH regulations, Canadian compliance for DIN, CFIA, CEPA, and Nonylphenol phase-out regulations.

    + Manage California Mill assessments for EPA products, sub-registrant relationships, and coordination with vendors.

    + Prepare letters of guarantee for food establishments, state and regional compliance in formulation and labeling for Phosphate, and annual EPA state registration.

    + Accountable for monthly, quarterly, and annual regulatory reporting and fees.

    + Communicate with internal/external customers regarding questions and requests for documentation related to regulatory activities.

    + Complete jurisdictional and company-specific safety paperwork on behalf of customers as requested.

    + Advise on storage, handling, and spill clean-up.

    + Attend seminars, conferences, and workshops to track new trends in regulatory activities and interact with trade associations and other regulatory professionals.

    + Prepare annual regulatory affairs budget.

    + Manage direct reports to support overall regulatory needs and provide regulatory support for affairs.

    Essential Skills

    + 7-10 years of regulatory experience in a chemical/product manufacturing environment.

    + 4-year college degree in Chemistry, Biology, or Environmental Science.

    + Knowledge of law and regulations.

    + Proficiency in Microsoft Office.

    + Time management skills.

    + Ability to work independently and with minimal supervision.

     

    Additional Skills & Qualifications

     

    + Law degree is desirable.

    + Minimum of 1 year of college-level math.

    Work Environment

    The role will involve collaboration with lab, field, and manufacturing teams. The physical requirements include standing for long periods and lifting up to 50 pounds.

    Pay and Benefits

    The pay range for this position is $100000.00 - $140000.00/yr.

     

    PTO, Holiday, Relocation package available, Medical, Dental, Vision

     

    Workplace Type

     

    This is a fully onsite position in Bowling Green,OH.

     

    Application Deadline

     

    This position is anticipated to close on Jul 30, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.