Integrated Resources
Job Title: Quality Auditor Associate
Location: Salt Lake City, UT 84108 - onsite
Duration: 5 Months+
Shift: 3rd shift (10 p.m. - 6:30 a.m. M-F, Onsite) Shift: 1st shift early (6 a.m. - 2:30 p.m. Mon - Fri)
Position: 1 Position
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 1yrs+ 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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Shift: 3rd shift (10 p.m. - 6:30 a.m. M-F, Onsite) Shift: 1st shift early (6 a.m. - 2:30 p.m. Mon - Fri)
Position: 1 Position
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 1yrs+ 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.
#sczr2