200+ applicants
STERIS · 3 days ago
Quality Engineer
Richmond, CA
Full-time
Onsite
Mid Level
$90K/yr - $104K/yr
1+ years exp
Wonder how qualified you are to the job?
Maximize your interview chancesBiotechnologyHealth Care
Hiring Manager
Helen Traylor
Insider Connection @STERIS
Responsibilities
Participate in cross-functional new product development teams with a focus on product/ service quality and Quality System compliance.
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 on 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.
Perform quality system audits and guide corrective actions.
Perform other duties as assigned.
Qualification
Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.
Required
Bachelor Degree in Engineering or Computer Science
1+ years of combined Manufacturing/Quality Engineering/Quality Systems experience or a minimum of 6 months on-site internship or co-op Quality focused experience
1+ years of experience with medical devices or other regulated industries preferred
1+ years of experience working in an ISO-certified environment is required
ASQ, QSR or familiarity with QSR/GMP regulations preferred
Excellent problem-solving skills
Focus on the identification of potential issues and continuous improvement
Experience working on cross-functional teams and on my own initiative
Demonstrated excellent organizational, oral, and written communications skills
Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint
Preferred
1+ years of experience with medical devices or other regulated industries preferred
1+ years of experience working in an ISO-certified environment is required
ASQ, QSR or familiarity with QSR/GMP regulations preferred
Experience with statistical analysis software and Visio preferred
Benefits
Medical insurance
Dental insurance
Vision insurance
Life insurance
Paid vacation time
Paid holidays
Tuition assistance
Company
STERIS
STERIS is a leading provider of infection prevention and other procedural products and services, focused primarily on healthcare, pharmaceutical and medical device Customers.
10,001+ employees
H1B Sponsorship
STERIS has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Trends of Total Sponsorships
2023 (10)
2022 (33)
2021 (18)
2020 (19)
Funding
Current Stage
Public CompanyTotal Funding
$0.28M2010-05-21Post Ipo Debt· $0.28M
1992-06-12IPO· nyse:STE
Leadership Team
D
Dan Carestio
President and CEO
W
Walt Rosebrough
CEO Emeritus & Senior Advisor
Recent News
2024-05-23
GlobeNewswire
2024-05-23
Company data provided by crunchbase
