Quality Manager
1 day ago
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.
The RoleThe Quality Manager in our Spartanburg, South Carolina facility is responsible for leading quality improvement for an Applied Sterilization Technologies (AST) processing or lab facility. This position leads implementing and maintaining state-of-the-art quality practices and assumes overall responsibility in ensuring that the site maintains operational and quality systems in a state of compliance to domestic and international standards.
Key Responsibilities- Lead the organization's Quality staff to ensure compliance to the overall Quality Management System and drive continuous improvement.
- Lead the organization's Quality staff to ensure alignment to operations, support Lean efforts and drive quality improvement for services/processes.
- Work closely with site senior management to provide strategic direction and development of the organization's quality strategies and tactics.
- Provide quality viewpoints and opinions on future service/technology offerings.
- Provide coaching, mentoring and leadership to the Quality staff.
- Serve as the site's Management Representative and lead the organization's Management Review process.
- Ensure compliance with appropriate domestic regulatory and international standards and requirements.
- Lead the organization's continuous improvement process; including data analysis, improvement projects and process capability to improve key metrics as measured by the product/service quality dashboard.
- Lead and implement effective production and process controls.
- Bachelor's Degree in a related scientific/technical field.
- Minimum of 5 years of people leadership experience, required.
- Minimum of 2 years of experience in a Quality leadership role.
- 10 years of experience working in an ISO certified environment required.
- 10 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
- 10 + years of experience in manufacturing or processing environment or another technical/scientific field.
- 10 years of experience with medical device or other regulated industries preferred.
- Sterilization experience preferred.
- Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.
- The opportunity to join a company that will invest in you for the long-term.
- STERIS couldn't be where it is today without our incredible people. That's why we share in our success together by rewarding you for your hard work.
- Hiring people who are in it for the long run with STERIS is our ultimate goal.
- We do this by providing competitive salaries, healthcare benefits, tuition assistance, paid time off, holidays, matching 401(k), annual merit, and incentive plans.
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