Associate Quality Control

Role: Associate Quality Control technician supporting microbiology and endotoxin testing for biopharma manufacturing, primarily in sterile, cGMP environments. Responsibilities include routine microbiological testing (bioburden, endotoxin, sterility), validation testing, data review, documentation, equipment maintenance, and participation in investigations and audits. The role emphasizes compliance with safety, cGMP, and regulatory standards. Requirements: high school diploma/GED with 2 years of quality experience, associate's with 6 months, or a bachelor's degree. Preferred skills include microbiology testing expertise (bioburden, endotoxin, microbial ID), experience with electronic systems (LIMS, CDOCS, Trackwise), and familiarity with GxP labs, Deviations, and TRAs. Experience with laboratory equipment, operational excellence initiatives, and strong communication skills are valued. High-value specifics: support for microbiology and endotoxin testing in sterile biopharmaceutical manufacturing, working within regulated environments, with a focus on documentation, validation, and compliance. Work setup: day shift (Monday-Friday, 7 am-3:30 pm). The role involves collaboration with manufacturing, quality, and compliance teams.