• Regulatory Specialist

    Actalent (Indianapolis, IN)


    Regulatory Specialist

    Description

    Corteva Agriscience™ is the only major agriscience company completely dedicated to agriculture. By combining the strengths of DuPont Pioneer, DuPont Crop Protection and Dow AgroSciences, we've harnessed agriculture's brightest minds and expertise gained over two centuries of scientific achievement. Our purpose is to enrich the lives of those who produce and those who consume, ensuring progress for generations to come.

     

    Pay per Hour Rate: $28.00 - $32.00

     

    Shift Timings:1st shift (8 AM - 5 PM), Monday–Friday

    Summary:

    Currently Corteva has a local opening as a Regulatory Specialist that they are looking to fill within their Scientific Writing group that support crop protection. The Scientific Writing Team drafts study reports and study summaries to support regulatory submissions for both biotech and crop protection products. Scientific Writers collaborate closely with stakeholders and customers including Study Directors and Monitors, Subject Matter Experts, Quality Assurance, Statisticians, and Global Registration Teams.

    Job Description:

    • Draft high-quality Product Chemistry study reports and study summaries to support Crop Protection regulatory submissions. Strong scientific writing skills and a experience in chemistry or related science are needed for drafting reports.

    • Perform quality control reviews on draft reports and/or raw data. An understanding of Good Laboratory Practice (GLP) is required.

    • Assist in developing new report templates, optimize processes, and assess stakeholder feedback for continuous improvement.

    • Facilitate finalization of reports and audit responses.

    • Communicate effectively with key stakeholders and customers. Partnership with stakeholders and customers to understand regulatory reporting requirements is important for success.

     

    Skills

     

    Document Control, Quality Assurance, Laboratory, QMS, Quality Management System, LIMS, Technical Writing, Scientific Writing, SOP Revision, SOP Review, SharePoint, Quality Control, Document Management, Document Review, Regulatory Documents, Research Reports

     

    Top Skills Details

     

    Document Control,Quality Assurance,Laboratory

     

    Additional Skills & Qualifications

    Must Have:

    1) Bachelors Degree in Life Science or related field

     

    2) Demonstrated experience in scientific writing (preferably within the regulatory or crop protection industry)

     

    3) Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines.

     

    4) Excellent attention to detail and ability to perform quality control reviews on scientific documents and raw data.

     

    5) Proficient in using Microsoft Office Suite and document management systems.

     

    6) Effective communication and collaboration skills with cross-functional teams and stakeholders.

     

    7) Ability to manage multiple projects simultaneously and meet tight deadlines.

    VMS Notes:

    1) BS Chemistry/BioChem, MS okay, PhD overqualified.

     

    2) Prior experience with scientific writing, GLP experience highly preferred

     

    3) Strong attention to detail, capable of writing technical documents while understanding chemistry discipline

    Experience Level

    Intermediate Level

     

    Job Type & Location

     

    This is a Contract position based out of Indianapolis, IN.

    Pay and Benefits

    The pay range for this position is $28.00 - $32.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a hybrid position in Indianapolis,IN.

     

    Application Deadline

     

    This position is anticipated to close on Jan 27, 2026.

    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.