Cell Lead II - Molding

Meier Tool & Engineering Brooklyn Park , MN 55443

Posted 2 weeks ago

Overview

About Cretex Medical

Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at www.cretexmedical.com.

Position summary:

The Cell Lead II will be responsible for coordinating, monitoring, and leading the activities of a cellular work team in support of assigned goals and objectives in a Quality Control environment. The Cell Leader II will manage employee time, approve time transactions in the ADP system, and will create performance related goals.

Responsibilities

Job Duties and Responsibilities

  • Create and optimize CMM programs using software such as PC-DMIS, Calypso, or similar

  • Develop inspection programs for vision inspection systems (e.g., OGP, Zeiss, Keyence)

  • Validate and maintain inspection programs to ensure alignment with part specifications and industry standards

  • Perform first article inspections, in-process inspections, and final inspections using CMMs and vision systems

  • Conduct measurement system analysis (MSA), including capability studies and gauge R&R analysis, to validate inspection methods

  • Interpret complex blueprints, CAD models, GD&T, and technical specifications for accurate measurement

  • Prepare detailed inspection reports, including capability analysis, MSA results, and data summaries

  • Troubleshoot and resolve technical issues related to metrology equipment and inspection software

  • Train and mentor junior metrologists and quality technicians in the use of CMM and vision inspection systems

  • Collaborate with cross-functional teams, including Engineering, Quality, and Production to support product development and manufacturing processes

  • Execute to the production schedule

  • Assign employees to run equipment and jobs

  • Ensure the area has the materials and supplies to meet production needs

  • Ensure jobs are completed and meet quality standards and are on time

  • Ensure machinery and equipment is running efficiently and effectively

  • Provide employees on-the-job training and mentoring

  • Ensure employees are following work instructions and processes

  • Provide daily updates through the Tier I process

  • Communicate production issues, schedules, and priorities within and between teams

  • Implement process improvements

  • Create employee goals, performance initiatives and areas of accountability that are directly aligned with the goals of the company

  • Ensure employees are following company guidelines, policies, and procedures

  • Manage the manufacturing ERP systems for production

  • Support and comply with the company Quality System, ISO, and medical device requirements

  • Read, understand, and follow work instructions and standard work

  • Partner with other business segments: sales/marketing, customer service, engineering, quality, and finance

  • Understand customer needs and the core business markets we serve

  • Ensure business systems are implemented, maintained, and functioning properly

  • Participate in required company meetings

  • Maintain an organized work area (5S)

  • Participate in the Operational Excellence Program

Qualifications

Job Requirements

  • High School Diploma or GED

  • 3 years of supervisory experience

  • 7 years of experience in manufacturing operations

  • Knowledge of manufacturing machinery, equipment, and processes

  • Knowledge of legal and regulatory requirements

  • Ability to manage relationships and team facilitation

  • Strong attention to detail

  • Strong problem-solving skills

  • Ability to prioritize work and manage multiple tasks

  • Ability to take direction from and give input to the next level leader

  • Ability to collaborate and assist team members

  • Ability to cross train in other areas of production when required

Preferred Knowledge, Skills and Abilities

  • Business/technical degree

  • Medical manufacturing experience

  • Familiar with ISO and FDA requirements

  • Certification in CMM programming or metrology (e.g., ASQ Certified Quality Technician, CMM Programmer)

  • Experience in a manufacturing environment with a focus on precision measurement and quality control

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