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Identifies trends, variances, deficiencies, and problems utilizing aggregated data and information as part of the integrated clinical documentation improvement program; performs provider and group level CDI data trend analysis, identifies issues and proposes solutions to leadership.
$104,811.2 a year depends on experienceFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Job Title: Documentation Specialist. Prior experience with Microsoft Office and eDMS or other applicable documentation system. This role requires the coordination, review, and revision of cGMP Documents, which include Standard Operating Procedures (SOPs), Work Instructions (WIs), FORMS, Job Aids (JAs), Specifications, Test Methods, and Manufacturing Batch Records.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Understanding of cGMP quality systems (e.g. change management and driving GDP within all documentation and records). Prior experience within Microsoft Office and eDMS (or other applicable documentation system.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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At Thermo Fisher Scientific, each one of our 65,000 extraordinary minds has a unique story to tell. When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe.
ExpandApply NowActive JobUpdated 2 days ago
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