Client SLC East: Quality Auditor Associate (contingent labor)
1st shift early (6 a.m. – 2:30 p.m. M-F)
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
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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1st shift early (6 a.m. – 2:30 p.m. M-F)
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
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.