Quality Documentation Auditor

Contract

Chicago,IL

Position Overview:

Detail oriented quality person with experience in QA/QC or auditing of documentation.  Responsibilities include quality review of documents generated during recovery, processing, cryopreservation, labeling, storage, and distribution of human allografts.  Experience with excel, word, and outlook required.

Essential Responsibilities:

• Responsible for quality review of documents generated during recovery, processing, cryopreservation, labeling, storage, and distribution of tissue.
• Responsible for making sure company is compliant with adhering to Good Tissue Practices established by FDA 21 CFR Part 1271, AATB and company procedures and policies.
• Auditing charts –Auditing Batch Records and Data Entry.
• Auditing labels and uploading documents into Vitals database.
• Audit RFA culture reports and file donor charts.
• Adheres to company policies, procedures, and documentation requirements.
• Treats others with courtesy, sensitivity, and respect at all times.
• Other duties as assigned.