Quality Engineer
Quality Assurance · Full-time
Mentor, OH, USA
USD 50-50 / hour
Posted on Oct 14, 2026
Quality Engineer II: Now Hiring
Mentor, OH | Onsite | Full-Time $50.00/hour
Ready to grow your quality career in a regulated, high-impact industry? Our Mentor, OH location is looking for a Quality Engineer II to help maintain and improve our quality system, support complaint and CAPA investigations, and drive product and process improvements.
Schedule (choose one)
Mon-Thu 7:00 AM-4:30 PM, Fri 7:00-11:00 AM
Mon-Thu 8:00 AM-5:30 PM, Fri 8:30 AM-12:00 PM
What You'll Do
? Compact 4.5-day work week with a short Friday
? Work that supports quality in a regulated industry
? Training and growth opportunities
Apply today!
Mentor, OH | Onsite | Full-Time $50.00/hour
Ready to grow your quality career in a regulated, high-impact industry? Our Mentor, OH location is looking for a Quality Engineer II to help maintain and improve our quality system, support complaint and CAPA investigations, and drive product and process improvements.
Schedule (choose one)
Mon-Thu 7:00 AM-4:30 PM, Fri 7:00-11:00 AM
Mon-Thu 8:00 AM-5:30 PM, Fri 8:30 AM-12:00 PM
What You'll Do
- Join cross-functional new product development teams, focusing on product quality and quality system compliance
- Develop sampling plans, designed experiments, capability studies, SPC, and trend analyses
- Lead or support corrective actions and problem-solving activities
- Create and update work instructions
- Analyze data and recommend process and product improvements
- Monitor and report on performance metrics
- Support evaluation and disposition of nonconforming materials
- Perform quality system audits and guide corrective actions
- Coach colleagues on quality principles and statistical techniques
- Support supplier quality improvement and compliance with ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, and EU MDR
- Bachelor's degree in Engineering
- 3+ years of manufacturing, quality engineering, and/or quality systems experience
- 3+ years working in an ISO-certified environment
- Strong problem-solving skills and a continuous improvement mindset
- Ability to communicate with facts and data and collaborate across departments
- Medical device or other regulated industry experience
- ASQ CQA or CQE certification
- Familiarity with QMSR/GMP regulations
- Proficiency in Excel, Word, and PowerPoint
? Compact 4.5-day work week with a short Friday
? Work that supports quality in a regulated industry
? Training and growth opportunities
Apply today!