Job Information
Cretex Medical Component and Device Technologies Quality Programmer / Cell Lead in 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 pr duction 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