*Dear Associate, Please check the below requirement and advise us the right consultant’s along with Rate, Availability, Contact Details, Current Location & Visa Status. It’s an immediate requirement please sent me the suitable resumes ASAP. Please make sure the candidate has all the required skills.Send me the resumes on Email: zia.k...@panzersolutions.com
Job Title: QA Analyst with clinical Location: Totowa NJ Duration: 12+ Months Contract No H1B Summary of Work Manage and track the review and approval of all Clinical Manufacturing & Packaging Batch Records, PSOs, Label proofs, SOPS, GLP CRO Audit Reports, Audit Responses, and Audit CAPAs. Maintain Master Documentation Vault. This includes the scanning of designated Master Documentation into automated storage databases. Retrieve all requested GLP/Clinical Manufacturing and Packaging related Master Documentation in a timely manner for all customers Coordinate scheduling of GLP CRO audits Coordinate review and approval of audit reports Scan and e-mail master GxP documentation to external departments and customers Scan all completed batch records into shared drive; file and archive to Master Documentation vault Maintain Batch Record Review logbook Perform Data verification and follow up Management and coordination of GLP/Clinical Supply Master Documentation Bachelor's Degree Best Regards, Zia Khan| Sr Technical Recruiter Panzer Solutions LLC Email: zia.k...@panzersolutions.com GTalk: zia.khn786 Voice : 203 652 1444 Ext: 120 * -- You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To post to this group, send email to reqsresumes@googlegroups.com. To unsubscribe from this group, send email to reqsresumes+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/reqsresumes?hl=en.
