Quality Programmer / Cell Lead

Overview:

About Cretex Medical

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:

• 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:

• 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

• 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