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TOMZ Corporation, a leader in manufacturing of devices and components for major medical device companies, is looking for a CMM Programmer to join our organization. TOMZ offers competitive compensation and excellent benefits, including 401k, health/dental, vision and paid time off. TOMZ maintains a modern, clean, and safe facility with state-of-the-art equipment and dedication to continuous process improvement. TOMZ is registered with the FDA as a Class 2 and Class 3 Medical Device Manufacturer and is certified to ISO 13485.
SUMMARY OF POSITION:
This position will be responsible for the activities associated with generation of inspection programs for commercial product and development programs. This role will be expected to establish programs, provide input on, and contribute to, fixturing and inspection method strategies and approaches.
- Must be knowledgeable of, and adhere to, the TOMZ Quality Management System.
- Generates, verifies, and operates CMM programs for first piece, in-process, and final inspections.
- Maintains CMM machines to include probe qualifications, regular cleaning and inspection of scales.
- Design fixtures needed to hold products for inspection during product development; sets criteria for instruments and specifications.
- Supports the development of inspection methods, tool mapping, First Article Inspections (FAI’s), and in process checks for manufacturing.
- Revises inspection programs and documents based on engineering changes, as required.
- Supports root cause investigation as applicable to CMM function, tooling, and programs.
- Contributes to process improvement; continually optimizes the inspection process by identifying bottlenecks and cost/time saving opportunities.
- Conducts training of designated CMM operators.
- Generates work instructions for CMM operation, cleaning, maintenance, etc.
- Support CMM operational and process qualifications including execution of Gage R&R activities.
- Other duties and responsibilities as assigned.
- High school diploma, GED, or equivalent directly transferrable work experience (Manufacturing or Engineering discipline preferred).
- Minimum of 3-5 years of experience in a regulated manufacturing environment.
- Regulated manufacturing industry experience (e.g. Aerospace, Defense, Pharmaceutical, etc.)
- Knowledge of and experience with GMP/ISO standards.
- Advanced knowledge of and the ability to read geometric dimensions and tolerances.
- Detailed knowledge of precision measuring instruments and their application, including but not be limited to, calipers, micrometers, depth gages, indicators, and plug and tread Go/No Go gages.
- Strong verbal and written English language communication skills.
- Competency with Microsoft Office (i.e. Outlook, Word, Excel, and PowerPoint), Adobe PDF, SolidWorks.
- “Hands-on” self-starter with ability to work both independently and as part of a team.
- Ability to work with a variety of functional areas, including R&D, Manufacturing, and QA, as required accomplishing results with minimal guidance.
While performing the duties of this job, the employee is frequently required to sit, talk and/or hear, and/or use hands to finger, handle, or touch objects, tools, or controls. The employee is occasionally required to stand, and/or walk. The employee must occasionally lift and/or move up to 10 pounds while moving files or small packages. The mental and physical requirements described here are representative of those that must be met by an individual to successfully perform the essential functions of this position.