*Dear Associate,
Please check the below requirement and advise us the right consultant’s
along with Rate, Availability, Contact Details, Current Location & Visa
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
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


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