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Cell Operations Manager
2 months ago
Cretex Medical Component and Device Technologies is seeking a highly skilled Cell Lead II to oversee the activities of a cellular work team in a Quality Control environment. The successful candidate will be responsible for coordinating, monitoring, and leading the team to achieve assigned goals and objectives.
Key Responsibilities- Program Development: Create and optimize CMM programs using software such as PC-DMIS, Calypso, or similar.
- Inspection Program Development: Develop inspection programs for vision inspection systems (e.g., OGP, Zeiss, Keyence).
- Validation and Maintenance: Validate and maintain inspection programs to ensure alignment with part specifications and industry standards.
- Measurement and Inspection: Perform first article inspections, in-process inspections, and final inspections using CMMs and vision systems.
- Measurement System Analysis: Conduct measurement system analysis (MSA), including capability studies and gauge R&R analysis, to validate inspection methods.
- Blueprint Interpretation: Interpret complex blueprints, CAD models, GD&T, and technical specifications for accurate measurement.
- Reporting and Troubleshooting: Prepare detailed inspection reports, including capability analysis, MSA results, and data summaries. Troubleshoot and resolve technical issues related to metrology equipment and inspection software.
- Training and Mentorship: Train and mentor junior metrologists and quality technicians in the use of CMM and vision inspection systems.
- Collaboration and Communication: Collaborate with cross-functional teams, including Engineering, Quality, and Production to support product development and manufacturing processes. Execute to the production schedule and ensure jobs are completed and meet quality standards and are on time.
- Leadership and Management: Assign employees to run equipment and jobs. Ensure the area has the materials and supplies to meet production needs. Ensure employees are following work instructions and processes. Provide daily updates through the Tier I process and communicate production issues, schedules, and priorities within and between teams.
- Process Improvement: Implement process improvements and create employee goals, performance initiatives, and areas of accountability that are directly aligned with the goals of the company.
- Quality and Compliance: Ensure employees are following company guidelines, policies, and procedures. Manage the manufacturing ERP systems for production and support and comply with the company Quality System, ISO, and medical device requirements.
- Education: High School Diploma or GED.
- Experience: 3 years of supervisory experience and 7 years of experience in manufacturing operations.
- Knowledge and Skills: Knowledge of manufacturing machinery, equipment, and processes. Knowledge of legal and regulatory requirements. Ability to manage relationships and team facilitation. Strong attention to detail and strong problem-solving skills.