Operator I - MN

Cynet Systems•Saint Paul, MN

About The Position

The Operator I works under direct supervision, performing routine and repetitive assembly operations and processes. The role maintains accurate job, traveler, and quality documentation; follows safety procedures; supports quality and continuous-improvement initiatives; performs routine and preventive equipment maintenance; and helps ensure parts are traceable and products meet quality requirements. The Operator communicates ideas, problems, and solutions to manufacturing management, works effectively with a self-managed team, and represents the company positively during tours and interactions with internal and external customers. The role supports divisional initiatives and applicable Quality Management Systems, Environmental Management Systems, and regulatory requirements. The work schedule shown is 3:00 p.m. to 1:30 a.m. Overtime may be required on Fridays and Saturdays based on business needs. The position requires use of a microscope for 50%–90% of the workday, depending on line assignment, and compliance with specified cleanroom clothing, footwear, and personal-appearance requirements.

Requirements

Ability to read, comprehend, and follow written procedures at a 7th-grade level and understand and follow verbal instructions at a 7th-grade level.
Understanding of and ability to use electronic data collection systems and computer software packages.
Ability to prioritize work by determining the sequencing and timing of 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.
Ability to use a microscope for 50%–90% of the workday, depending on line assignment.
Ability to work overtime on Fridays and Saturdays based on business needs.
Comply with specified clothing, footwear, and appearance requirements, including wearing clean, non-shedding clothing that covers the torso, upper arms, and legs and fits under required lab clothing; closed-toe, closed-heel shoes with socks or stockings; and no makeup, nail polish, artificial nails, strong fragrances, or unsafe jewelry or piercings. Religious or cultural head coverings are permitted if fully covered by required PPE. Open wounds must be covered with a bandage.

Nice To Haves

Six months of experience working in a medical or other regulated production environment.
Previous medical device, manufacturing, or assembly experience.
High school degree or equivalent preferred.

Responsibilities

Ensure job documentation for cell operations and functions is accurate and up to date.
Communicate ideas, problems, and solutions clearly to all levels of manufacturing management, both orally and in writing.
Represent the company positively during tours by demonstrating techniques and sharing appropriate information.
Support company policies and procedures and maintain a positive attitude when interacting with internal and external customers.
Follow safety guidelines and use appropriate safety devices during all operations.
Participate in continuous-improvement and quality initiatives to improve production processes and meet quality and profitability metrics.
Perform routine and preventive maintenance on applicable equipment to maximize efficiency, minimize accidents, and extend the life of equipment and tools.
Maintain accurate traveler and quality records, ensure parts are traceable, and support resolution of quality issues.
Participate with the Manufacturing Supervisor or Manager in setting and monitoring individual goals and cell performance metrics.
Support divisional initiatives and applicable QMS, EMS, and other regulatory requirements.
Apply troubleshooting and interpersonal skills, including conflict resolution, active participation, active listening, cooperation, and flexibility, to support a successful self-managed team.
Demonstrate a basic understanding of Lean Manufacturing and continuous improvement.