Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control (QC) Analyst I is responsible for conducting routine analysis of GMP and ISO materials under general supervision and in accordance with standard operating procedures (SOPs). The individual compiles data for documentation of test procedures, prepares reports, and maintains lab equipment. The QC Analyst I uses existing procedures to solve routine or standard problems and performs basic troubleshooting under guidance or supervision. Occasional travel between sites may be required.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
501-1,000 employees