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Manufacturing specialist Jobs in Noblesville in
Manufacturing Technical Writer
Global Channel Management, IncIndiana, United States- Promoted
Senior Project Manager - Pharmaceutical, Manufacturing - IN
Michael PageCarmel, IN, United States- Promoted
Commissioning Specialist
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- Promoted
Industry X - Digital Manufacturing Specialist
AccentureCarmel, IN- Promoted
Manufacturing Director
MondelēzIndiana, US- Promoted
- New!
MANUFACTURING MAINTENANCE MECHANIC - 2ND SHIFT
Dairy Farmers of AmericaIN, United States- Promoted
Manufacturing Environmental Health & Safety Manager
O-ILapel, IN, USRegional Manufacturing Maintenance Manager
WestRockIN WFH IndianaAdvance Manufacturing Engineering Intern
Schlage Lock Company LLCCarmel, IN- Promoted
- New!
MANUFACTURING MAINTENANCE TECH 2 OR 3
Continental AGIN, United StatesAdditive Manufacturing Account Manager
GoEngineer IncCARMEL, Indiana, United States, 46032Logistics Specialist
Isotopia USAWestfield, IN, USManufacturing Technician
Curium Live ForwardNoblesville, IN, United StatesManufacturing Chemist
Cardinal HealthIndiana, United States- Promoted
Manufacturing Manager - 236808
Medix™IN, United States- Promoted
SAP Manufacturing Solution / Process Integration Architect
MAK Technologies LLCIN, 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.