Quality Engineer

Location: Waltham, MA
Department: Azzur of NE, LLC

Job Description

Azzur Group is seeking an accomplished Quality Engineer to work with a pharmaceutical client in the Boston, MA area
Responsibilities and Duties:
  • General quality compliance support, with emphasis on helping to build the GxP Training program
  • Supplier documentation and audit writing, as well as general support to the Supplier Qualification Team
  • Auditing experience in a GMP realm (or even GCLP/GCP) would be a plus
  • QMS/Quality Systems experience as we build out their systems (Veeva experience is ideal)

Requirement

  • BS in Engineering, Science or equivalent technical
  • 3-10 years’ of quality engineering or related experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device
  • Excellent written and verbal communication skills; excellent technical writing
  • Ability to work effectively in a fast paced multitasking environment.
  • Strong working knowledge of FDA and cGMP regulations and documentation
  • Proficient in Microsoft Word, Excel, PowerPoint.
  • Ability to travel to client sites throughout the New England


Azzur Group is an equal opportunity employer and promotes diverse cultures, ethnicities, gender, and ages in our workplace. We believe that promoting diversity plays an important role in developing top-quality talent, fostering greater innovation and creativity, and enhancing our relationships with customers and the communities in which we operate.


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