Quality Assurance Programmer/Analyst - Medical
Listed on 2026-01-01
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Quality Assurance - QA/QC
Quality Engineering, Quality Control / Manager -
Manufacturing / Production
Quality Engineering
Join to apply for the Quality Assurance Programmer/Analyst - Medical role at Techtronic Industries - TTI
Techtronic Industries is a fast-growing world leader in Power Tools, Accessories, Hand Tools, Outdoor Power Equipment, and Floor Care for DIY, professional, and industrial users. The company is committed to transforming these industries through environmentally friendly cordless technology. Our brands RYOBI and HART are renowned worldwide for their quality, performance, safety, and innovation.
Job SummaryA Metrology professional responsible for creating inspection programs for coordinate measuring machines (CMM) and other metrology tools. The candidate should have experience with GD&T, reading CAD models, and evaluating CMM data for accuracy. This role involves testing the quality of parts supplied by external manufacturers.
Responsibilities / Skills- Support Quality and Manufacturing with dimensional feedback for parts.
- Program, operate, and interpret data from CMM, Vision Systems, and other measurement tools.
- Set up, operate, perform basic maintenance, and troubleshoot CMM equipment.
- Conduct studies on measurement methods such as repeatability, correlation, and Gage R&R.
- Understand how CMM programs calculate data.
- Establish standard fixturing for consistent measurements.
- Use metric measuring instruments like calipers and micrometers.
- Document inspection results according to Quality Assurance procedures.
- Train staff on metrology tools.
- Participate in continuous improvement initiatives.
- Associate's degree or equivalent experience in a related field.
- 2-4 years of experience in metrology with CMM programming.
- Self-directed, detail-oriented, dependable, and able to work independently.
- Strong communication skills and a sense of urgency.
- Training in Metrology topics.
- Proficiency in Microsoft Office Suite.
- Experience working with senior management.
- Knowledge of FDA 21 CFR 820 and ISO 13485 is a plus.
- Professional certifications are a plus.
- Experience with Minitab, SAP, and CMM Manager is advantageous.
- Seniority Level: Mid-Senior level
- Employment Type:
Full-time - Job Function:
Engineering and IT - Industry: Manufacturing
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