Please Note: This is a night shift opportunity that follows a 2-2-3 schedule. It will be eligible for a shift differential.
Job Summary
The QA Manufacturing Specialist is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems, and governmental regulations.
This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for on the floor review of executed records (batch record section review, solution records, equipment records, and logbooks) supporting all aspects of cGMP operations. Client and regulatory audit/inspection support is also within job scope.
Job Responsibilities
Perform on-the-floor compliance review on executed records including batch records, equipment preparation records, and solution record and associated forms, in...