QA Associate Specialist – Document Control
1 week ago
TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.
Our client, a leading pharmaceutical company is hiring a QA Associate Specialist – Document Control on a contract basis. Please only local candidates to Summit NJ.
Work Location: Summit NJ
Pay: $30-31/hour W2
Required Skills:
• Document Control & Reporting experience
• Veeva experience preferred
• Technical troubleshooting
• The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP
Document Control operations for Cell Therapy organization
• Managing an electronic document system which includes reviewing and approving document
change requests, troubleshooting and releasing documents to an effective state
• May write and revise document control procedures including participating in the
development and roll-out of document control tools
• Follow Policies, SOPs, and work instructions to support the document approval process,
assign effective dates and training workflows, and archive documents and document change
requests
• Assist with cross-training of Document Control personnel and customers to ensure adherence
with procedures
• Execute the process and procedures for identifying, collecting, distributing and filing the
controlled documents for the site
• Generate document management system reports for Quality Council metric reporting
• Support internal and external audits and regulatory inspections if required
• Assist with document retrieval /organization support during regulatory inspections
• Provide communication as to the status of Quality Systems deliverables to customers,
management, and stakeholders
• Some technical writing skill set and be able to critically review documents while effectively
inputting and expressing Quality principles
• Relevant document control experience in a cGMP/FDA regulated environment
• Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality
Systems (e.g. Document Management System, Quality Management System)
• Experience interacting with FDA or other regulatory agencies strongly preferred
• Strong knowledge of cGMPs and domestic regulatory requirements
• Knowledge of manufacturing quality (manufacturing, packaging, facilities, critical systems,
validation, etc.)
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