Quality Programmer / Cell Lead
Cretex Medical Component and Device Technologies

Brooklyn Park, Minnesota


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 Quality Programmer / Cell Lead 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 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



Get Hired Faster

Subscribe to job alerts and upload your resume!

*By registering with our site, you agree to our
Terms and Privacy Policy.

More Engineering jobs


Schweitzer Engineering Laboratories
Chattanooga, Tennessee
$88,000.00 - $108,000.00 per year
Posted about 1 hour ago
Schweitzer Engineering Laboratories
Boise, Idaho
$100,900.00 - $168,100.00 per year
Posted about 1 hour ago
Schweitzer Engineering Laboratories
Fairview Heights, Illinois
$17.00 - $28.50 per hour
Posted about 1 hour ago
View Engineering jobs ยป

Share diversity job

Quality Programmer / Cell Lead is posted on all sites within our Diversity Job Network.


African American Job Search Logo
Hispanic Inclusion Jobs Logo
Asian Job Search Logo
Women Inclusion Jobs Logo
Diversity Inclusion Jobs Logo
Seniors to Work Logo
Black Inclusion Jobs Logo
Veteran Job Center Logo
LGBT Job Search Logo
Asian Inclusion Jobs Logo
Disabled Job Seekers Logo
Senior Inclusion Jobs Logo
Disability Inclusion Jobs Logo
US Diversity Job Search Logo
LGBTQ Inclusion Jobs Logo
Hispanic Job Exchange Logo