Operator II - 1st Shift

The Opportunity

This position works out of our Plymouth, MN, location in the Electrophysiology (EP) business. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

As an Operator, you’ll be working under general supervision in accordance with specific procedures and practices may perform a combination of assembly, weld, x-ray, repair, and test operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, electronic systems, and related medical device assemblies.

What You’ll Work On

• Ensure that relevant job documentation for cell operations and functions is accurate and up to date
• Troubleshooting skills
• Interpersonal skills such as conflict resolution, active participation, active listening, interpreting, cooperation, and flexibility to allow for a successful self-managed team
• Be able to clearly communicate ideas, problems, and solutions to all levels of manufacturing management in both written and oral form
• Positively represent the company during tours by demonstrating techniques and sharing appropriate information
• Positively represents and supports the company’s policies and procedures
• Maintain a positive attitude when interacting with internal customers and external customers, such as tours
• Follow safety guidelines and utilize appropriate safety devices when performing all operations
• Participate in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics
• Perform routine/preventative maintenance on applicable equipment to maximize efficiency, minimize accidents to enhance longer life of equipment and tools
• Maintain accurate records to ensure traveler and quality documents are accurate, all parts are traceable, and quality issues can be addressed to assure the quality of all products
• Demonstrates a basic understanding of Lean Manufacturing
• Demonstrates a basic understanding of continuous improvement
• Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations
• Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements

Required Qualifications

• High School Diploma / GED
• Minimum 2 years of experience working in a medical or other regulated production environments
• Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions
• Understanding of and ability to utilize electronic data collection systems and computer software packages
• Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance
• Ability to handle and maneuver small components and parts
• Ability to make critical decisions and judgments with minimal supervision

Preferred Qualifications

Previous medical device, manufacturing, or assembly experience is helpful