Quality Engineer
Company: STERIS
Location: Mentor
Posted on: March 17, 2023
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Job Description:
At STERIS, we help our Customers create a healthier and safer
world by providing innovative healthcare and life science product
and service solutions around the globe.
Position Summary
The Quality Engineer designs, installs and evaluates quality
assurance process systems, procedures and statistical techniques;
plans, conducts, and follows up on supplier audits; recommends
revision of specifications when indicated; assists in the
development, maintenance and improvement of the organization's
overall supplier quality system in accordance with the requirements
of ISO, FDA QSR and STERIS policies.
May conduct training on quality assurance concepts and tools.
Interfaces with all other engineering components within the company
and with customers and suppliers on quality related issues.
Duties
1. Major responsibilities of the role would include but are not
limited to, (a) leading supplier quality improvement projects to
drive improvement in supplier cost, quality and delivery, (b)
driving improvement to supplier quality measurement and scorecard
systems, (c) leading general product quality improvement efforts to
drive improvement to key quality metrics, and (d) leading
production and business process improvement efforts
cross-functionally in the business.
2. Drive improvement in key quality metrics as measured by the
product/process SQDC program
3. Coordinate improvement projects such as projects, complaint
investigations, CAPA, raw material trends, and other continuous
improvement actions.
4. Assist in creating, maintaining and improving overall Quality
System integrity to ensure compliance to ISO and QSR standards.
5. Drive timely and effective root cause analysis and provide
quality engineering leadership to suppliers.
6. Address and resolve supplier quality issues.
7. Directly support the customer complaint management process and
assist in resolution in accordance with customer needs and
compliance standards as it relates to suppliers.
8. Serve as quality engineering support to new product development
design, testing, and introduction ensuring the attainment of key
quality deliverables and quality targets.
9. Conduct material improvement team meetings. Resolve disputes and
reach consensus on actions to be taken.
10. Oversee Approved Supplier List, Supplier Quality
agreements/questionnaires, and establishing yearly critical
supplier schedule.
11. Perform all other duties as assigned.
Education Degree
Required Experience
1. 3 - 5 years' experience with manufacturing processes (such as
Chemical, formulation, molding, and assembly.)
2. 3 - 5 years' experience in quality systems, science, or
engineering.
3. Excellent problem-solving skills including FMEA or root cause
analysis and implementation of Supplier Corrective and Preventive
Actions.
4. Leadership ability to coordinate projects in a cross-functional
team environment.
5. Demonstrate effective organizational, oral and written
communications skills
6. Demonstrated computer skills and experience with applications
such as EXCEL, Minitab, Word.
#LI-BN1
STERIS is a leading provider of products and services that meet the
needs of growth areas within Healthcare: procedures, devices,
vaccines and biologics. We exist to fulfill our MISSION TO HELP OUR
CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD. STERIS is a $3B,
publicly traded (NYSE: STE) company with approximately 16,000
associates and Customers in more than 100 countries.
If you need assistance completing the application process, please
call 1 (440) 392.7047. This contact information is for
accommodation inquiries only and cannot be used to check
application status.
STERIS is an Equal Opportunity Employer. We are committed to equal
employment opportunity and the use of affirmative action programs
to ensure that persons are recruited, hired, trained, transferred
and promoted in all job groups regardless of race, color, religion,
age, disability, national origin, citizenship status, military or
veteran status, sex (including pregnancy, childbirth and related
medical conditions), sexual orientation, gender identity, genetic
information, and any other category protected by federal, state or
local law. We are not only committed to this policy by our status
as a federal government contractor, but also we are strongly bound
by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics
required by - 60-741.44(k), shall be available to all employees and
applicants for employment for inspection upon request. The program
may be obtained at your location's HR Office during normal business
hours.
Req ID: 34889
Job Category: Quality
Keywords: STERIS, Mentor , Quality Engineer, Engineering , Mentor, Ohio
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