Quality Auditor Associate

SGS_JOB_1877

Pharmacy
 Utah
MS Office
GMP

Contract - 04+ Months (Contract)

Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a moderate scope and complexity of activity. Work Schedule: 1st shift early (6 a.m. – 2:30 p.m. M-F) and 3rd shift (10 p.m. – 6:30 a.m. M-F, Onsite)

Job Responsibilities:

  • Perform sampling and delivery of intermediate and finished products.
  • Assist with retain sample management.
  • Conduct monthly GMP and batch-specific room audits.
  • Perform in process record review of commercial manufacturing batch records.
  • Review completed swab data and performed subsequent room/equipment release.
  • Ensures compliance with all Company policies and procedures, including safety rules and regulations.
  • Performs related duties as assigned.

Skills:

  • Requires a minimum of one year experience in a regulated environment such as pharmaceutical, medical device, nutraceutical, or food processing industries.
  • Requires basic understanding of Good Manufacturing Practice (cGMP) and the application to a production environment.
  • Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems.

Education/Experience:

  • Associate’s degree or higher (or equivalent) achieved or in process preferred.

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