Inprocess Quality Assurance Associate ILocation: US-NJ-East WindsorHigh School Diploma or Equivalency.Up to 2 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.Responsibilities:Collaborates with other production staff and departments.Accurately and consistently completes and documents batch records/other required paperwork.Maintaining various logbooks to document the performance or completion of specific functions.Maintaining IPQA supply inventory.Qualifications:Ability and willingness to learn manufacturing/packaging procedures and federal regulations pertaining to manufacturing process.Experienced in proper documentation and correction practices.Must be a team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, and Supply Chain to meet finished product release goals.Be able to work long hours to support production requirements.Be available for overtime, including weekends, as needed for production support.
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