Job Purpose
The Quality Assurance (QA) Batch Record Reviewer performs the Technical and Final release function of the graft release process. The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately determines and documents the final disposition of each graft on the controlled batch records and in the VIVEX Biologics computer system. This position requires attention to detail and must be performed in accordance with standard operating procedures, as well as all applicable state, regulatory and AATB requirements.
Duties and Responsibilities
2. Work closely with operations and customer service personnel on inventory needs for customer orders and back orders.
3. Knowledgeable of the VIVEX BTM computer system and able to perform all functions as required.
4. Responsible for reporting all variances, errors and deviations to Quality Assurance.
5. Able to collaborate on complaint and/or nonconformance reports according to VIVEX procedure.
6. Performs other duties as assigned by the Manager and Director of the Department.
Qualifications
Working Conditions
Primarily a quiet office-oriented work environment. Some evening and weekend work may be required to ensure customer commitments and goals are met.
Physical Requirements
While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds.
Direct Reports
No direct reports.
QA Batch Record Reviewer • Miami, FL, US