QA Associate

West Greenwich, RI 02817

Posted: 07/15/2016 Employment Type: Contract Industry: Process Development Job Number: 1741

  In this role you will be supporting the Corporate Product Quality department through the entry, verification, review, tracking, and archiving of technical data.

Required skills include knowledge of GMP, 2-3 years operational experience in pharmaceutical or regulated industry; data entry; data verification; clerical and/or administrative experience; proficient in MS Excel, Word, PowerPoint, MS Project

*GMP experience 1+ years. 
*Quality 1+years of experience. 
*Technical Writing 1+ years of experience. 
*Preferred bachelor in Life Sciences

The successful candidate will: 
• Perform transcriptional data verification of technical reports and other documents, following corporate Standard Operating Procedures. 
• Enter documents into corporate quality GMP Lab databases, checking for completion and correctness. 
• Enter data from external sources into MS Excel spreadsheets or MS Word documents. 
• Gather documents and materials, collates, distributes and/or files. 
• Enter and distribute documents and forms. 
• Data processing support to include maintaining database for all documentation. 
• Audit reports and files for discrepancies. 
• May compile information and metrics from various documents or databases. 
• Provide guidance or refer staff members to appropriate contacts. 
• Coordinate or manage multiple documents and team members through the document review and approval process following corporate SOPs. 
• Communicate via telephone, instant message, voice-mail, meetings, teleconferences, and/or e-mail.

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