QA Document Control Specialist

Fremont  ‐ Onsite
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Keywords

Description

Responsibilities:
  • Provide support for processing controlled documents through the change control process
  • Edit documents that are being routed for changes and revision ensuring that changes are accurately tracked
  • Work with reviewers of documents to ensure that review of documents are performed in a timely manner
  • Issue DCRs
  • Track in-process DCRs and obtain signatures
  • Compilation and filing of documents
  • Scanning and archiving


Candidate must possess:
  • BA/BS degree in Science or equivalent with at least four years of direct QA document control experience in the biotechnology or pharmaceutical industry
  • Must have experience with MS Word, Adobe Acrobat Professional, MS Excel, PowerPoint, SharePoint
  • Must have strong knowledge of cGMPs and cGCPs
  • Proven record working in a fast-paced multi-disciplinary project team environment
  • Excellent oral and written communication skills


To find out more about Real please visit www.realstaffing.com
Start date
05/2013
Duration
12 months
From
Real Staffing
Published at
24.05.2013
Project ID:
541172
Contract type
Freelance
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