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Manufacturing Technical Writer
Global Channel Management, IncIndiana, United States- Promoted
Anime Content Writer
VirtualVocationsFort Wayne, Indiana, United States- Promoted
Korean Freelance Writer
OutlierFort Wayne, IN- New!
Outlier is hiring : Swedish Freelance Writer in Fort Wayne
MediabistroFort Wayne, IN, United StatesContracted Grant Writer
Cardinal Services of IndianaFort Wayne, IN, USADirector of Data Content and Strategy
LexisNexis Risk Solutions FL Inc. CompanyIndiana- Promoted
- New!
Manager, Human Resources
Ingram Content GroupFort Wayne, IN, United StatesOrder Writer / Merchandiser
Boar’s Head BrandWestford, CTSr Content and Policy Analyst
World Compliance, Inc. CompanyIndiana- Promoted
Administrative Assistant
Ingram Content Group LLCFort Wayne, IN, United StatesFreelance Writer
WebProps.orgFort Wayne, IN, USFull Time Nabisco Merchandiser / Order Writer
Mondelēz InternationalIndiana, United StatesManufacturing Technical Writer
Global Channel Management, IncIndiana, United States- Full-time
Manufacturing Technical Writer needs 7 years' experience
Manufacturing Technical Writer requires :
Willing to perform testing in a laboratory environment using automated laboratory equipment
Word, Excel, PPT
Able to reference company standards to meet regulatory guidelines
Lead validation documentation efforts
Able to capture software develop terms and transfer Subject Matter Experts knowledge to documents
May be asked to perform system test cases in a laboratory setting
Expert in creating new design requirements documents including User requirements, System Overview and Configuration, Validation and Security Plans required for GMP automation platforms.
Manufacturing Technical Writer duties :
Support the manufacturing, quality assurance, engineering and a variety of other departments by incorporating subject matter expert comments into well-constructed and easy-to-read approvable documents.
Edit / write a variety of technical articles, reports, manuals, flow charts, and other documentation for a wide range of uses, including GMP operations and validation activities.
Edit / create presentations, charts, diagrams, graphics, and research documentation. Write test scripts.
Assist data entry, report generation, accuracy checks and tracking. Assist in assembly of validation package documents for GMP libraries.