Manufacturing Quality & Inspection Tech – 2nd Shift (M-F 3:00 PM – 11:30 PM)

Role: Perform quality inspections of finished biopharmaceutical products to ensure compliance with specifications and regulatory standards. Responsibilities: conduct visual and instrumental tests, document non-conformances, prepare inspection certifications, and collaborate with production teams to improve manufacturing quality. Requirements: high school diploma or GED, basic computer skills, understanding of quality inspection processes, and ability to follow instructions; capable of working in a regulated environment. Preferred: experience with medical device quality systems, familiarity with Oracle or EDHR systems. High-Value: role supports biopharma quality assurance in a regulated environment, emphasizing compliance with industry standards and documentation; potential experience with medical devices relevant to biopharma manufacturing. Work Setup: on-site with flexibility for overtime; based in the U.S., not including visa sponsorship.