The Senior Manager, Quality is responsible for leading quality improvement for complex or multi-site manufacturing or service facilities. This position takes the lead in developing, adopting, and maintaining state-of-the-art quality practices for sites which have multi-faceted product/service lines and associated regulatory requirements. The Senior Manager, Quality assumes overall responsibility in ensuring that the site maintains operational and quality systems in a state of compliance to domestic and international standards. The role is responsible for the organization, documentation, and maintenance of the quality system to be compliant with, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR and other applicable standards. This role leads the local site(s) efforts focused on product/service quality improvement, supplier quality, process quality, new product/service development quality and quality system compliance. The Senior Manager, Quality serves as the Management Representative for the site(s) and is responsible for ensuring the quality system meets all applicable regulatory standards.
- Lead the organization’s Quality staff to ensure compliance to the overall Quality Management System and drive continuous improvement.
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Lead the organization’s Quality staff to ensure alignment to manufacturing and servicing operations, support Lean efforts, and drive quality improvement for products and services.
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Work closely with Senior Management to provide strategic direction and development of the organization’s quality strategies and tactics.
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Provide quality viewpoints and opinions on future product and service development.
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Provide coaching, mentoring, and leadership to the Quality staff.
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Serve as the site’s Management Representative and lead the organization’s Management Review process.
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Ensure compliance with appropriate domestic regulatory and international standards and requirements.
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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.
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Lead and develop effective production and process controls.
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Manage the complaint handling processes to insure customer responsiveness and product and process improvements.
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Ensure compliance to the New Product Development process and assurance that the Product Requirements Document includes key quality performance metrics.
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Assess new designs for manufacturability, testability and reliability to ensure the Quality risks and deliverables of the New Product Development process meet the required application reliability and design intent.
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Determine supplier qualification risks based upon criticality of component and supplier process capability.
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The position requires a level of authority to conduct and direct required activities such as quality planning, personnel management, and regulatory compliance.
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This individual has autonomy to perform the duties of Person Responsible for Regulatory Compliance (PRRC) on behalf of STERIS legal manufacturing entities under the EU MDR. This individual shall suffer no disadvantage within the organization in relation to proper fulfilment of his or her duties in lieu of article 15 of the EU MDR.
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Perform other duties as assigned.
Required:
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Bachelor’s Degree (Engineering or related technical field).
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Minimum 10 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
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Minimum 10 years of experience working in an ISO certified environment.
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Minimum of 6 years in a Quality leadership role.
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Must fulfil the experience requirements listed in Article 15 of the EUMDR (PRRC).
Preferred:
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Minimum 10 years of experience with medical device or other regulated industries.
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ASQ, QSR or familiarity with QSR/GMP regulations.
Other:
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Excellent problem-solving skills
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Focus on identification of potential issues and continuous improvement.
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Experience working on cross-functional teams and on own initiative.
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Demonstrated excellent organizational, oral, and written communications skills.
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Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
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Experience with statistical analysis software and Visio preferred.
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.
Here is a brief overview of what we offer:
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Market competitive pay
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Extensive paid time off and (9) added holidays
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Excellent healthcare, dental, and vision benefits
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Long/short term disability coverage
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401(K) with company match
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Maternity and parental leave
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Additional add on benefits/discounts for programs such as pet insurance
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Tuition reimbursement and continued educational programs
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Excellent opportunities for advancement in a stable long-term career
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Pay range for this opportunity is $124,737.50 - $154,087.50. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity 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.
