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Quality Assurance Specialist
3 months ago
We are seeking a highly skilled Quality Engineer to join our team at STERIS. As a Quality Engineer, you will play a critical role in ensuring the quality and integrity of our products and services.
Key Responsibilities- Develop and implement statistically valid sampling plans, designed experiments, capability studies, SPC, and trend analysis.
- Initiate and/or participate in process and product corrective actions and problem-solving activities.
- Update/establish documented work instructions as needed.
- Review collected data to perform statistical analysis and recommend process/product changes to improve quality.
- Monitor and report on performance metrics.
- Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
- Collaborate with other departments and facilities within the company on quality-related issues.
- Maintain product integrity and quality through support of evaluation and disposition of nonconforming materials.
- Bachelor's degree preferred.
- 1-5 years of combined Manufacturing/Quality Engineering/Quality Systems experience or minimum of 6 months on-site STERIS internship or co-op experience.
- 1-5 years of experience with medical device or other regulated industries preferred.
- 1-5 years of experience working in an ISO certified environment required.
- ASQ, QSR, or familiarity with QSR/GMP regulations.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. We offer a dynamic and supportive work environment, opportunities for professional growth and development, and a competitive compensation package.
We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced Quality Engineer looking for a new challenge, please submit your application.