Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition for products across all value streams to ensure product meets acceptable quality limits based on FDA regulations.
Responsible for entering in-process inspection results as required for Acceptable Quality Limits and defect recognition in manufacturing systems such as SAP, POMS and Laboratory Information Management System.
Responsible for accurate documentation and compliance with Good Documentation Practice requirements of the tasks performed.
Manages quality sampling across multiple production lines in accordance with the production schedule in a timely manner.
Effectively executes assigned tasks and priorities with minimal supervision and seeks additional guidance when problems are the beyond scope of training or knowledge.
Elevates higher level safety, quality, technical and operating issues/details in a timely manner to the appropriate group.
Provides support for improvement opportunities in the areas of documentation, procedures, processes and equipment through cross functional team interaction.
Collaborates with others to maintain a positive atmosphere to accomplish business objectives and fosters positive working relationships.

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Technician I, Manufacturing QA (2ND Shift M-F 3PM-11PM)