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QA Specialist - Auditing

Mt. Prospect, IL
An established Biotechnology company is looking to hire an experienced Quality Assurance Specialist to their team. This position offers valuable industry knowledge, experience within a clinical research environment, a fast-paced work environment, and experience leading projects pertaining to pre-clinical studies. 

  • Coordinate and perform quality assurance operations in accordance with GLP regulations. 
  • Write and review SOPs and other documentation as it pertains to clinical studies. 
  • Will be trained in FDA and EPA regulations. 
  • Will get experience in auditing various studies. 
  • Must have a BS in Biology, Chemistry, or related science.
  • 1 - 3 years of experience within a cGLP/GMP regulated environment is required.
  • Must have the ability to take on responsibility, pay close attention to detail and communicate with multiple departments.
  • Very strong written and verbal communication skills are required
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