Quality Manager

The Role

The 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. The role is responsible for the organization, documentation and maintenance of the quality system to be compliant with, as appropriate, the following standards: ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads the local site efforts focused on quality system improvement, supplier quality, process quality, new service/modality/technology development quality and quality system compliance. The Quality Manager serves as the Management Representative for the site(s) and is responsible for ensuring the quality system meets all applicable regulatory standards. The Quality Manager has the responsibility, duty and decision-making authority to put any product on hold that is identified as potentially non-conforming and escalating as needed for additional reviews by technical teams.

Relocation assistance to Spartanburg, South Carolina area available. 

What You Will Do

• 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.

What You Will Also Do

• Manage the CAPA, complaint and non-conformance handling processes to insure customer responsiveness and process improvements. 
• Lean and manage Regulatory Agency and Notified Body inspections and drive the creation and implementation of sustainable and effective remediation plans.
• Oversee the completion of Customer audits. 
• Apply regulatory knowledge and judgment to the evaluation of quality concerns and regulatory compliance issues. 
• Travel to other AST facilities, domestically and/or globally, to support remediation activities, audits/inspections and/or continuous improvement initiatives. 
• Demonstrate commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations. 
• The position requires a level of authority to conduct and direct required activities such as quality planning, personnel management and regulatory compliance. 
• Perform other duties as assigned.

What You Will Need to Be Successful

• 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. 

Preferred Experience

• 10 years of experience with medical device or other regulated industries preferred.
• Sterilization experience preferred.
• Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.

Skills

• Excellent problem-solving skills
• Focus on identification of potential issues and continuous improvement.
• Experience working on cross-functional teams and on own initiative.
• Effective interpersonal skills, ability to work independently under minimal guidelines and supervision.
• Demonstrated excellent organizational, oral and written communications skills.
• Must have working familiarity of MS Office applications including Excel, Word, and PowerPoint.
• Ability to work in a fast-paced, regulated environment with strict deadlines and ever-changing responsibilities.
• Mathematical skills including practical application of fractions, percentages, ratios, proportions, and algebra. 

What STERIS Will Offer You

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.  Join us and help write our next chapter.

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