The Temporary Quality Control (QC) Technician performs a range of quality control activities, including receiving and inspecting raw materials, conducting in-process and finished product inspections, supporting Supply Chain Quality and the Returned Goods Authorization (RGA) process, and reviewing Device History Records (DHRs). The role supports compliance with applicable quality standards and regulations and uses facility inspection and test equipment for mechanical and visual evaluations. The technician also performs assigned audits, investigations, and tests, processes non-conformance material reports (NCMRs) through the QC area, and enters data into the NCMR database. This position requires 2–4 years of Quality Control experience in the medical device, pharmaceutical, or biotechnology industry, with working knowledge of FDA and ISO regulations. An associate degree or equivalent is desired but not required. The technician must be able to read technical drawings, procedures, and regulations; perform practical mathematical calculations; work with minimal supervision and in a team; and lift items weighing up to 35 pounds. Current U.S. work authorization is required.
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