Quality Auditor Associate
3rd shift (10 p.m. 6:30 a.m. M-F, Onsite)
Salt Lake City, UT
5 Months (possible extension)
Screenings:
The QA roles WILL require the physical please, as a lot of their work is in the MFG space.
Candidate start date: Goal is September 8th
The job requirements include the following essential areas of responsibility:
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 perform subsequent room/equipment release.
Ensures compliance with all Company policies and procedures, including safety rules and regulations.
Performs related duties as assigned.
Education/Certification/Experience:
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.
Associate s degree or higher (or equivalent) achieved or in process preferred.
Skills/Knowledge/Abilities:
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems.
Self-directed with ability to organize and prioritize work
Ability to communicate effectively with excellent written and oral communication skills
Ability to interact positively and collaborate with co-workers and management
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