Quality Control Analyst Protein Sciences
Responsible for conducting routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures. Compiles data for documentation of test procedures and prepares reports. Calibrates and maintains lab equipment. May develop testing methods. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis and other such duties and responsibilities as may from time to time be reasonably assigned. All employees are responsible for training on, understanding, and following documented procedures which apply to their departments that support the Quality System.
-Education: BS/MS level degree in a relevant science, biomedical or pharmaceutical technical education with experience in and/or knowledge of documentation and quality systems or the combination of experience and training that is equivalent
-2-3 years working experience in a GLP/GMP environment preferable
-Fluent in English both oral and written
-Experienced in relevant computer software
||1000 Research Parkway |
Meriden, CT 06450