Senior Quality Systems Engineer / Quality Control Specialist

Qnity; Chesterfield (MO); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Comprehensive pay and benefits package

Job summary

Qnity in Chesterfield, MO is looking for a Quality Manager to oversee the implementation and improvement of the Quality Management System. The role involves maintaining site metrics and ensuring compliance with quality standards like ISO 9001.

The ideal candidate will have 7-10 years of experience managing a QMS and possess strong communication skills. They will also coordinate QMS audits and lead investigations into quality non-conformances.

Qualifications

• 7-10 years' experience managing a QMS certified to ISO 9001:2015.
• Lead or Internal Auditor certification for ISO 9001:2015 desired.
• Leadership and project management skills to drive improvement projects.

Responsibilities

• Maintain site metrics and communicate with leaders on quality performance.
• Coordinate and participate in QMS audits by Certification Bodies.
• Lead investigations on internal and 3rd party Non-Conformances.

Skills

Proficient knowledge of ISO 9001

Good communication skills

Attention to detail

Experience performing Internal Audits

Experience with CAPA systems

Education

Bachelor's degree in a related field

Tools

Microsoft Office

Job description

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics.

At Qnity, we’re more than a global leader in materials and solutions for advanced electronics and high-tech industries – we’re a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting‑edge technology possible. We value forward‑thinking challengers, boundary‑pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jump‑start your career with us.

Responsibilities

• Implementation, support, and improvement of the Quality Management System (QMS) for this site.
• Maintain site metrics and communicate with business and quality leaders on site quality performance; review recommended areas for focus and attention.
• Support QMS interfaces with other manufacturing sites; this location is a remote support location for other sites.
• Maintain and improve conformance to applicable Quality Standard requirements including ISO 9001, IATF 16949, AS9100, etc.
• Coordinate and participate in QMS audits by 3rd party Certification Bodies (CB); act as liaison between site team and CB.
• Coordinate, maintain and improve internal audit program in compliance with Quality Standards and any relevant customer specific requirements.
• Coordinate Management Review activities for Chesterfield and support of other manufacturing sites.
• Conduct training on QMS procedures as required and maintain associated records.
• Improve and maintain documented information control activities, including revision of the Quality Manual, development of document reviews, and control of related records.
• Lead Corrective Action activities; monitor completion of assigned investigations and corrective actions; conduct verification of effectiveness.
• Lead investigations on internal and 3rd party NCs; improve and maintain employee competence in problem solving.
• Coordinate and track continual improvement projects; evaluate effectiveness to customer or business goals/impact.
• Analyze data and trends in support of QMS processes and other site activities such as customer service, customer satisfaction, complaints, or quoting.
• Support the Document Change Management process for the Chesterfield site.
• Additional administrative responsibilities and support for other functions at the site as needed.

Requirements

• Proficient knowledge of ISO 9001 (minimum), IATF 16949 and AS9100D desirable.
• Good communication skills, both written and oral.
• Ability to maintain accuracy and attention to detail.
• Ability to work as an individual contributor or in a team environment.
• Experience performing Internal Audits.
• Experience with CAPA systems.

Education / Experience

• Bachelor’s degree in a related field (Quality Mgmt., Operations, Manufacturing Mgmt., etc.).
• Minimum 7‑10 years’ experience working within and/or managing a QMS certified to ISO 9001:2015 (IATF 16949 desired).
• Lead or Internal Auditor certification for ISO 9001:2015 and/or IATF 16949:2016 (desired).
• Ability to understand relevant industry controls and requirements in support of manufacturing support processes to achieve and maintain compliance with relevant standards.
• Leadership and project management skills to drive improvement projects.
• Root Cause/Corrective Action training and experience.
• Proficiency in Microsoft Office applications and any other relevant systems for the management of documents, corrective actions, projects, etc.

Location

On‑site, Chesterfield, MO

Equal Opportunity Statement

Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class.

Qnity offers a comprehensive pay and benefits package.