What are the responsibilities and job description for the Quality Engineer position at United Pharma Technologies Inc?
Position: Quality Engineer
Location: Tempe, AZ (On-site)
Duration: 12 months
Role Summary:
Quality Engineer responsible for ensuring quality and regulatory compliance in the development and manufacturing of Class III implantable cardiac and neuromodulation medical devices, with a focus on inspection optimization and microelectronics manufacturing.
Key Responsibilities:
- Lead inspection optimization projects (manual and automated inspections)
- Support process development, validation, and equipment qualification (IQ, OQPQ)
- Partner with process engineers on test method development and validation (Gage R&R, MSA)
- Maintain and apply quality standards for manufacturing operations
Required Qualifications:
- Bachelor’s degree with 4 years or Master’s degree with 2 years relevant experience
- 4 years in medical device manufacturing and process quality/engineering
- Experience in microelectronics, wafer fab, SMT, or chip & wire assembly
- Strong knowledge of ISO, FDA-GMP, and structured problem-solving (DMAIC, 8D)
- Proficiency in Microsoft Office tools