Senior Operator

Abbott • Minnetonka, MN

20h • Onsite

About The Position

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Their portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Their 115,000 colleagues serve people in more than 160 countries. In Abbott’s Electrophysiology (EP) business, they are advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. This position works out of the Minnetonka location in the EP division. The main purpose of this role is to support the assigned area Production Supervisor in ensuring the continuous flow of high-quality production through assigned work-cells in accordance with manufacturing obligations. The Senior Operator acts as the lead person in self-directed cells or teams and assists in ensuring that high levels of productivity and product quality are consistently maintained, and helps coordinate efforts towards their continuous improvement.

Requirements

• High School Diploma / GED
• Minimum 4 years related experience in the assembly of digital and analog circuitry/devices, including the demonstrated ability to provide work/lead direction to a team.
• Must be able to demonstrate comprehensive product assembly techniques, related process knowledge, plus a mastery of appropriate skill sets as confirmed by cognizant Engineering and/or Production/Quality Assurance supervisory personnel.
• Prior experience working in an air-conditioned clean-room manufacturing environment is required.
• Demonstrated ability to read and understand engineering drawings, schematics, diagrams, notes, and layouts.
• Demonstrated ability to use frequently used hand tools; demonstrated eye-hand coordination and capable of working with small precision devices.
• Experience working in a broader enterprise/cross-division business unit model preferred.
• Ability to work in a highly matrixed and geographically diverse business environment.
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Demonstrated verbal and written communication, interpersonal, organizational and basic math skills.
• Ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to maintain regular and predictable attendance.
• Occasional scheduled overtime is a requirement of this position.

Nice To Haves

• Minimum 5 years medical device or related assembly experience is preferred.

Responsibilities

• Responsible for coordinating production activity in assigned work areas, ensuring that product is continuously processed in accordance with build schedules.
• Coordinates communication of work instructions to personnel in designated areas in accordance with supervisory objectives.
• May perform direct manufacturing operations in support of build schedules, as directed or as necessary.
• Performs regular process and quality performance audits of personnel, tooling and equipment in assigned areas.
• Advises supervisor or other appropriate contact in the event of issues affecting the productivity of the cell.
• Accumulates information for assigned areas regarding work in process inventory status and daily output quantities.
• Assists in providing direct training to area operators as required.
• Provides feedback on defects encountered, and provides re-training support as necessary.
• Accumulates and organizes data to support area continuous improvement plans, as directed.
• Provides assistance in expediting priority product and tasks in assigned areas.
• Performs inspection and determines disposition of rejects per required documentation, as directed.
• Resolves and/or facilitates resolution of problems including identifying causes to prevent re-occurrence.
• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
• Performs other related duties and responsibilities, on occasion, as assigned.

Benefits

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
• Health and wellness benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees