NorthWest Biotherapeutics Inc (NWBO)

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Job description: QC Document Specialist I position.

(Cognate Website December 14, 2017.)

Cognate Bioservices Inc in Memphis, TN is seeking applicants for the QC Document Specialist I position. Applicants will be expected to have experience with reviewing cGMP documentation with strong attention to detail. Reporting to the QC Ops Manager, this position will be responsible for receiving completed documentation from QC analysts for review of calculations and documentation practices.
Essential Duties / Responsibilities
Receives and reviews results from QC Analytical group for completeness and accuracy.
Data entry into QA metric logs, reviewing electronic data entries
Recognize GDP and calculation errors in QC documentation, and ensure the correction of those errors
Data entry of product analytical test results in QC tracking and trending spreadsheets/software
Comprehend QC assay procedures, calculations, and expected documentation practices in order to enforce compliance through peer review of completed documentation
Maintain an organized document review system
Assist in compiling QC data packets when needed
Assist with document and record control functions as needed
Qualifications
Bachelor’s or higher degree in a science related field, or 2 years of experience in a cGMP lab environment
Strong attention to detail
Strong math skills and demonstrated knowledge of life sciences
Knowledge of GDP, GMP, and GLP
Very organized with the ability to prioritize and multi-task requests
Good computer skills (MS Word and Excel)
Good written and verbal communication skills
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