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.
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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