Operator I - MN

Abbott Laboratories•St. Paul, MN

1d•Onsite

About The Position

The Operator I is responsible for producing high-quality medical devices and equipment in an ESD manufacturing environment, not a clean room. Work includes assembling or packaging capital equipment similar to computers. Under close supervision, the operator may perform a combination of assembly, repair, and test operations on capital equipment such as computers and generators. Assignments follow specified or standardized procedures and are closely and continually reviewed. The role is 100% onsite in St. Paul, Minnesota, with daytime hours Monday through Friday, 7:00 AM–3:30 PM. The position requires a commitment to 40 hours per week and no absences during the first 30 days. Overtime is relied upon, and the amount may vary from week to week. The stated duration is 12 months. The operator maintains accurate, up-to-date job documentation and records, including traveler and quality documents, and helps ensure part traceability and timely resolution of quality issues. The role supports safety, continuous improvement, quality initiatives, Lean Manufacturing, divisional initiatives, and applicable Quality Management Systems, Environmental Management Systems, and other regulatory requirements. Business-casual attire is specified, subject to detailed production-area clothing and footwear rules.

Requirements

English communication skills, written and verbal.
Ability to recognize colors.
Commitment to 40 hours per week and no absences during the first 30 days.
Experience following manufacturing processes.
Ability to read, comprehend, and follow written procedures and understand and follow verbal instructions.
Ability to use electronic data collection systems and computer software packages.
Ability to prioritize work by sequencing and timing jobs according to precedence and importance.
Ability to handle and maneuver small components and parts.
Ability to make critical decisions and judgments with minimal supervision.

Nice To Haves

ERP experience.
Background in medical device or other regulated environments.
High school degree or equivalent.

Responsibilities

Perform assembly, repair, test, or packaging operations on capital equipment according to specified or standardized procedures.
Ensure job documentation for cell operations and functions is accurate and up to date.
Maintain accurate traveler and quality records, ensure parts are traceable, and support addressing quality issues.
Communicate ideas, problems, and solutions clearly in written and oral form to manufacturing management at all levels.
Maintain a positive attitude when interacting with internal customers and external customers, including tours.
Follow safety guidelines and use appropriate safety devices during operations.
Participate in continuous improvement and quality initiatives to improve production processes and meet quality and profitability metrics.
Demonstrate a basic understanding of Lean Manufacturing.
Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics.
Support divisional initiatives and applicable QMS, EMS, and other regulatory requirements.