Upvote
Downvote
Specialist, QA II
Share Job
- Suggest Revision
- As the Specialist QA II you will be responsible for shop floor monitoring, clearance, and record review during aspects of parenteral manufacturing which includes, but is not limited to raw material release, compounding, aseptic filling, lyophilization, inspection, labeling, and packaging.
- Perform AQL sampling and inspection of raw materials, and inspected, labelled, and finished products according to ANSI/ASQ Z1.4 standards and approved procedures.
- Perform batch record review for all production steps – ensure compliance to established and validated parameters.
- Train on and Support Controlled (Grade C and D) and Aseptic (Grade A and B) processing areas with Line Clearances, QA oversight, and batch record review (MBR and EBR).
- based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance.
Active Job
Updated 7 days agoSimilar Job
Relevance
Active