Seeking highly motivated Aseptic Manufacturing Technician. Job Summary: Work in a controlled environment, adhere to GMP, and maintain the highest quality standards. Perform tasks related to the preparation, assembly, and sterilization of drug products, ensuring cleanliness, safety, and efficacy of aseptic drug products. Key Responsibilities: Operate and monitor sterile manufacturing equipment (filling machines, autoclaves, aseptic processing equipment); follow SOPs and regulatory guidelines (GMP, FDA); perform sterilization and filtration; maintain accurate production documentation (batch records, QC checks, equipment logs); assist with setup, cleaning, and sanitization; conduct routine inspections and maintenance; collaborate with QA/QC; monitor/report production metrics; adhere to health and safety protocols; participate in training. Qualifications: HS diploma or equivalent and certificate in Bioprocess Technology (Associate degree or higher preferred); prior pharma or sterile manufacturing experience highly desirable; knowledge of GMP and sterile practices; familiarity with aseptic techniques; attention to detail; troubleshooting ability; strong communication and teamwork; ability to work in fast-paced, regulated environment; willingness to work shifts, weekends, holidays as needed. Physical Requirements: lift up to 30 lbs; stand/sit for extended periods; work in cleanroom with PPE. QCL offers competitive salaries, excellent benefits, and subsidized childcare.