Want to know if you’re a fit? Upload your resume and let our AI show you.
Skills
Capital Equipmentunmatched
Cleanroomunmatched
Communication Skillsunmatched
Computer Softwareunmatched
Continuous Improvementunmatched
Data Collectionunmatched
Documentationunmatched
ERP (Enterprise Resource Planning)unmatched
English Languageunmatched
Environmental Management Systemsunmatched
Establish Prioritiesunmatched
Healthcare Qualityunmatched
High School Diplomaunmatched
Lean Manufacturingunmatched
Manufacturingunmatched
Manufacturing Managementunmatched
Manufacturing/Industrial Processesunmatched
Medical Equipmentunmatched
Performance Metricsunmatched
Problem Solving Skillsunmatched
Profit & Lossunmatched
Quality Assuranceunmatched
Quality Managementunmatched
Quality Metricsunmatched
Record Keepingunmatched
Regulatory Requirementsunmatched
Description
Operator I St. Paul, MN (Onsite) Location: St. Paul, MN 55117 100% onsite Schedule: Monday Friday, 7:00 AM 3:30 PM (OT available; amount varies week to week) Duration: 3 6 month contract, possible extension
Position Overview
This is an ESD manufacturing environment not a clean room. The role involves assembly and/or packaging of capital equipment (similar to computers). The Operator I is responsible for the production of high-quality medical devices and equipment. Working under close supervision, this person may perform a combination of assembly, repair, and test operations on capital equipment such as computers and generators. Key Responsibilities
Perform routine assignments according to specified and/or standardized procedures; work is closely and continually reviewed.
Ensure relevant job documentation for cell operations and functions is accurate and up to date.
Maintain accurate records so travelers and quality documents are correct, all parts are traceable, and quality issues can be addressed.
Clearly communicate ideas, problems, and solutions to all levels of manufacturing management, both written and verbal.
Follow safety guidelines and use appropriate safety devices during all operations.
Participate in continuous improvement and quality initiatives to enhance production processes and meet quality and profitability metrics.
Work with the Manufacturing Supervisor/Manager to set and monitor individual goals and cell performance metrics.
Support divisional initiatives in line with Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Maintain a positive attitude with internal and external customers, including facility tours.
Required Qualifications
English communication (written and verbal) and color recognition.
Commitment to 40 hours/week with no absences in the first 30 days.
Ability to read, comprehend, and follow written procedures, and understand verbal instructions.
Ability to use electronic data collection systems and computer software packages.
Ability to prioritize work by sequencing and timing 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.
Basic understanding of Lean Manufacturing.
Preferred Qualifications
Experience following manufacturing processes; ERP experience preferred.
Background in medical device or other regulated environments.