×
Register Here to Apply for Jobs or Post Jobs. X

Scientific Writer-- GOEDC

Job in Zionsville, Boone County, Indiana, 46077, USA
Listing for: Compunnel Inc.
Full Time position
Listed on 2026-01-28
Job specializations:
  • Research/Development
    Research Scientist, Medical Science, Clinical Research
Salary/Wage Range or Industry Benchmark: 30 - 33.8 USD Hourly USD 30.00 33.80 HOUR
Job Description & How to Apply Below
Position: Scientific Writer-- GOEDC5713045

Job Title:
Regulatory Specialist-Scientific Writer

Duration: 12+ Months

Location: Indianapolis, IN 46077

Pay Rate: $30 - 33.80/hr on W2 (all inclusive)

Job Summary:

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 Summary

  • Draft high-quality Product Chemistry study reports and study summaries to support Crop Protection regulatory submissions. Strong scientific writing skills and a background 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.

Job Requirements and Qualifications:

  • Bachelor’s degree or higher in Chemistry, Biochemistry, or a related scientific discipline.
  • Demonstrated experience in scientific writing, preferably within the regulatory or crop protection industry.
  • Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines.
  • Excellent attention to detail and ability to perform quality control reviews on scientific documents and raw data.
  • Proficient in using Microsoft Office Suite and document management systems.
  • Effective communication and collaboration skills with cross-functional teams and stakeholders.
  • Ability to manage multiple projects simultaneously and meet tight deadlines.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary