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Job Description

The Associate Director of Quality Control manages the Quality Control department to ensure that product standards are met or exceeded. S/he is responsible for the Quality Control testing of all Enzymatics products, including new and existing proteins, product formulations, buffers, nucleic acids, and reagent kits. 

Position responsibilities also include the development and implementation of new analytical and functional tests, creation and execution of product stability plans, and periodic re-testing of inventoried products. The Associate Director is also responsible to maintain close communications and a high level of service to internal stakeholders whose processes rely on Quality Control for success, including the Research, Applications Development, Sales Support and Manufacturing departments. 

The Associate Director will serve as Radiation Safety Officer.

  • 4+ years of managerial experience, prefer more than 5 years in non-academic industry experience and/or equivalent combination of education and experience

  • Experience with ISO 13485 certification and federal regulations 21 CFR 820 and 21 CFR Part 11

  • Experience in a Good Manufacturing Practice (GMP) environment

  • Strong Molecular Biology Applications background

  • Working experience with radioactive materials desired

  • Drive and Determination

  • Demonstrated Scientific “problem solving” skills

  • Positive external and internal relationship management skills

  • Strong communication and presentation skills

  • Proven ability to thrive in change oriented environment

  • Self Starter



  • Bachelor's degree from four year college or university in Life Science discipline

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