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QA Specialist
Ref No.: 18-07076
Location: Rockville, Maryland
Provide bioanalytical support for the production of biopharmaceutical products Responsible for running GMP samples on various methods. Responsible for following standard operating procedures to maintain cGMP compliance. Maintain laboratory equipment and facilities. Calibrate laboratory instrumentation. Mechanical aptitude and familiarity with cGMP's is required. Word processing and database software (I.e. MS Word and Excel). Bachelor's Degree in Chemistry or Biochemistry with 1-3 years of experience.