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Document Specialist
| Details |
Country: USA
Location: CA South San Francisco
Total applied: 19
Relevant Work Experience: 1+ to 2 Years
Career Level: Experienced (Non-Manager)
Education Level: Bachelor's Degree
Job Type: Temporary / Contract / Project
Job Status: Full Time
Job Shift: First Shift (Day)
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Document Specialist
Major Biotech with a location in South San Francisco is seeking a Document Specialist to join their team.
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Description:
The Clinical Quality Assurance (QA) Documentation Specialist will be responsible for supporting Clinical QA operations in the data entry associated with clinical tickets and batch records; verification of data and generation of reports associated with ticket review and lot release activities. The individual will also work with product managers to support the compiling, review, and verification of product specification document data in support of clinical quality manufacturing documentation.?
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Requirements:??
Familiarity with electronic database systems and data record entry and review. Specific knowledge of GMP systems,Filemaker Pro, NovaManage and Livelink is a plus.?? BA/BS or equivalent?
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Key Words:? Quality Assurance, Clinical, Data, Database, Filemaker, Document, California
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Biotechnology and Pharmaceutical 
