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Document Specialist I-26229  

Permanent
Description
  • Works with primary originators of documentation to translate the documentation into written form.
  • Coordinates and ensures that documentation is written, edited, reviewed and approved in a timely manner to meet established deadlines.
  • Issues document change requests and documentation status reports, files technical reports and master SOPs and associated historical data, writes departmental SOPs.
  • Ensures GLP and/or cGMP documentation is correct, clear, and consistent.
  • Updates and maintains document as well as other databases.
  • Provides guidance to other employees, as needed.
  • Assists with cGMP documentation training.
Performs data entry for tracking documents.

Qualifications
  • High school diploma required with 3-5 years related experience, Bachelor's degree with 1 year preferred.
  • Experience with Livelink, Access, Catsweb, MS Office.
  • Excellent typing, editing and proofing skills required.

Job: Quality
Primary Location: United States-Massachusetts-Framingham
Shift: Day Job
Job Type: Regular
Employee Status: Regular.

LocationUnited States-Massachusetts-Framingham
CountryUnited States of America
CompanyGenzyme
ContactGenzyme
Web Linkhttp://www.genzyme.com
ReferenceJS26229
Posted Date05/26/2011 01:03:09
 
 
 
 
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