Sr Validation Engineer

Location: Los Angeles Consulting
Department: Azzur of CA, LLC

Job Description

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)
  • Equipment and tooling qualifications/validations.
  • Protocol/report writing and execution.
  • Tooling design and FAI.
  • Writing procedures and creating production routers
  • Test method development and validation
  • Other tasks may be assigned to satisfy project requirements with pre-approval of Azzur team management.

Requirement

  • BS in Engineering, Science or equivalent technical
  • 3-10 years of quality engineering or related experience in a regulated, manufacturing environment within the medical device industry
  • 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.

 



Apply Now

Life Science Moves FAST

Stay in the know by signing up for our newsletter. We’ll share company successes, industry must-know information, and keep you updated on the latest events you don’t want to miss.