Aequor
Title: Quality Auditor Associate
Read the overview of this opportunity to understand what skills, including and relevant soft skills and software package proficiencies, are required. Duration: Salt Lake City Utah Duration: 06+ months with possibility of extension Shift– 1st shift early (6 a.m. – 2:30 p.m. M-F) OR 3rd shift (10 p.m. – 6:30 a.m. M-F, Onsit e) Job Description: 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
Read the overview of this opportunity to understand what skills, including and relevant soft skills and software package proficiencies, are required. Duration: Salt Lake City Utah Duration: 06+ months with possibility of extension Shift– 1st shift early (6 a.m. – 2:30 p.m. M-F) OR 3rd shift (10 p.m. – 6:30 a.m. M-F, Onsit e) Job Description: 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