Quality Assurance Technical Writer
Medasource, Lebanon, IN, United States
18 month contract with possibility of extensions
Lebanon, Indiana
Job Summary: The Quality Assurance Technical Writer will be working with the quality compliance team to help with document management and technical writing during startup phases of the new GMP site.
Responsibilities: Develop, edit, and maintain technical documents, including SOPs, required tools, protocols, and reports.
Experience with utilities, manufacturing equipment, or laboratory equipment is preferred
Collaborate with subject matter experts to ensure accuracy and clarity.
Ensure consistency, readability, and compliance with company and industry standards.
Assist in document revision and version control as necessary.
Qualifications: 3-5 years of pharma GMP technical writing experience
Experience with Veeva Quality Docs is preferred
Ability to work in different functional areas
Writing clear and easy to understand documents for people with a HS diploma and a PhD.
#J-18808-Ljbffr
Lebanon, Indiana
Job Summary: The Quality Assurance Technical Writer will be working with the quality compliance team to help with document management and technical writing during startup phases of the new GMP site.
Responsibilities: Develop, edit, and maintain technical documents, including SOPs, required tools, protocols, and reports.
Experience with utilities, manufacturing equipment, or laboratory equipment is preferred
Collaborate with subject matter experts to ensure accuracy and clarity.
Ensure consistency, readability, and compliance with company and industry standards.
Assist in document revision and version control as necessary.
Qualifications: 3-5 years of pharma GMP technical writing experience
Experience with Veeva Quality Docs is preferred
Ability to work in different functional areas
Writing clear and easy to understand documents for people with a HS diploma and a PhD.
#J-18808-Ljbffr