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Document Control Assistant

Manpower-Lakewood, CO

A Lakewood area company is in need of a Document Control Assistant. This position will run through the end of the year and will conclude by February. The successful candidate will have extensive experience working with MS Word. General duties include standardization of format, editing content, and formatting. Coding macros is a plus but usage of established macros is necessary. Basic working knowledge of MS Access is also necessary. The successful candidate will have extensive experience with advanced Word functions. The position will require flexibility and rapidly changing priorities. Att...
 

Document Control Assistant Jobs in Denver, Colorado Jobs

Manpower | Lakewood, CO, 80228 |
A Lakewood area company is in need of a Document Control Assistant. This position will run through the end of the year and will conclude by February. The successful candidate will have extensive experience working with MS Word. General duties include standardization of format, editing content, and formatting. Coding macros is a plus but usage of established macros is necessary. Basic working knowledge of MS Access is also necessary. The successful candidate will have extensive experience with advanced Word functions. The position will require flexibility and rapidly changing priorities. Att...
 
 

Manpower Jobs

Manpower Professional | Huntsville, AL | >5
Quote Specialist, If you could design your ideal position, what would you include? The opportunity to use your skills and experience fully? To make a strategic contribution? Rewards and recognition for your contributions? Growth potential? Whether you are pursuing a contract or permanent placement, Manpower Professional knows how and where to make your plans come to life. Develops quotes and costing summaries for contract items. Generates quotes and E-rate proposals for library and school system services. Develops quotes for other proposed network connections, upgrades, and services. Track ...
Manpower Professional | Redwood City, CA | >6
Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports). Review/approval of engineering study protocols/reports and validation study protocols/reports. Review and approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree and 5-8 years of direct experience in the field. Recent experience with Class III implantable medic...
 
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