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