Abbott

healthcare

2ndshiftQualityTechnicianII

$0–0k Minnetonka, Minnesota, United States FULL TIME
The Brief

“2nd shift Quality Technician II at Abbott. Skills: Quality control, Documentation review, Compliance. Ensure documentation complies with procedures. Audit and verify processes”

What You'll Achieve.

Support sustainability of commercially released product; Ensure manufacturing processes meet daily production schedules; Enhance productivity and product quality; Assure all products conform to compliance requirements

Industry & Context.

healthcare
Eligibility Requirements

Ability to work 2nd shift hours (M-Th 2:30 PM - 12:30 AM CST with occasional overtime on Fridays), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Work in a clean room environment

What They're Looking For.

Must Have

H.S. diploma, equivalent or at least 2 years of experience as a QA Technician or areas related to quality control., Experience at medical devices companies or equivalent, Applies acquired knowledge of procedures and practices and a complete understanding of fundamentals in a functional area and working knowledge of other related disciplines., Will perform this job in a quality system environment., Some Microsoft Office - Handles MS Word, Power Point and Excel at a basic to intermediate level, Some Basic math knowledge- Basic Math calculations, Ability to work within a team and as an individual contributor in a fast-paced, changing environment., verbal and written communications with ability to effectively communicate at multiple levels in the organization., Multitasks, prioritizes, and meets deadlines in timely manner., organizational and follow-up skills, as well as attention to detail, Ability to work 2nd shift hours (M-Th 2:30 PM - 12:30 AM)

Nice to Have

Prior medical device experience preferred.

What You'll Do.

Ensure documentation complies with procedures

Audit and verify processes

Review and verify compliance of documentation

Notify supervision of issues or errors

Execute testing of samples

Identify and segregate nonconforming material

Input data to required systems

Comply with FDA regulations

How You'll Work.

Team & Collaboration

Maintaining positive and cooperative communications and collaboration with all levels of employees.; Maintaining a collaborative partnership with cross-functional team members

Communication Scope

verbal and written communications with ability to effectively communicate at multiple levels in the organization.

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