Quality Auditor Associate - Meet Life Sciences : Job Details

Description

Quality Auditor Associate

Screenings:

The QA roles WILL require the physical please, as a lot of their work is in the MFG space.

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