Operator I_MN ONLY – 2nd Shift

Operator/Assembler 2nd Shift Role

Location: Minnetonka, MN 55345

12+ Months of contract role

2nd shift schedule – 3:30 pm to 2:00 am

2nd shift interview – Monday, July 20th 4:30 PM – 6:00 PM

Main Purpose of Role

As an Operator I, you'll work under direct supervision, performing routine and repetitive assembly operations and processes.

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

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

Prefer 6 months of experience working in a medical or other regulated production environments Previous medical device, manufacturing, or assembly experience is helpful High school degree or equivalent preferred