Quality Assurance Auditor - Good Manufacturing Practices ChanTest
THIS JOB HAS EXPIRED This position will be responsible for implementing and sustaining cGMP (21 CFR part 211) compliance for the R&D and Cell Biology departments. Specific responsibilities include SOP implementation, instrument calibration and process validation infrastructure. Provide site guidance to ensure Federal, State, Local and Corporate compliance. Maintain the current Quality System and update as needed; also provide the site?s quality approval. Act as quality liaison to R&D and Cell Biology.
Candidates must be self-motivated with the ability to prioritize and handle multiple deadline-driven projects, with a strong attention to detail. B.S. in Chemistry, Biology, Chemical Engineering or related science, along with 5-7 years of FDA-regulated, quality laboratory experience. Thorough understanding of FDA current GMPs, as well as chemical and laboratory safety requirements, along with general knowledge of use and operation of laboratory equipment.
||14656 Neo Parkway |
Cleveland, OH 44128
THIS JOB HAS EXPIRED