Job Description

We are seeking a detail-oriented and analytical Quality Management System Engineer to join our team in Wichita, United States. In this role, you will be responsible for developing, implementing, and maintaining comprehensive quality management systems that ensure organizational compliance with industry standards and regulatory requirements. You will work collaboratively across departments to drive continuous improvement initiatives and foster a culture of quality excellence throughout the organization.

• Design, develop, and implement quality management systems aligned with relevant industry standards (ISO 9001, ISO 13485, AS9100, or equivalent)
• Conduct internal and external audits to assess compliance with established quality procedures and regulatory requirements
• Analyze quality data and metrics to identify trends, root causes, and opportunities for process improvement
• Develop and execute corrective and preventive action (CAPA) plans to address quality issues and prevent recurrence
• Create and maintain comprehensive quality documentation, including policies, procedures, work instructions, and process maps
• Perform failure mode and effects analysis (FMEA) and risk assessments to proactively identify and mitigate potential quality risks
• Collaborate with cross-functional teams to implement process improvements and operational efficiencies
• Provide training and guidance to employees on quality procedures, standards, and best practices
• Monitor and report on key performance indicators (KPIs) related to quality metrics and system effectiveness
• Stay current with regulatory changes and industry standards to ensure ongoing organizational compliance
• Support management reviews and continuous improvement initiatives to enhance overall system performance

Qualifications

• 3+ years of professional experience in quality management, quality assurance, or quality control roles
• Demonstrated expertise in quality management system standards (ISO 9001, ISO 13485, AS9100, or similar)
• Strong proficiency in root cause analysis methodologies and corrective/preventive action (CAPA) processes
• Experience with audit procedures, compliance documentation, and regulatory requirements
• Solid understanding of process improvement methodologies such as Lean, Six Sigma, or Kaizen
• Proficiency with data analysis tools and statistical software for quality metrics evaluation
• Experience with failure mode and effects analysis (FMEA) and risk management frameworks
• Familiarity with enterprise resource planning (ERP) or manufacturing execution systems (MES)
• Excellent technical writing skills with the ability to create clear, comprehensive documentation
• Strong organizational and project management skills with the ability to manage multiple initiatives simultaneously
• Excellent communication and interpersonal skills with the ability to collaborate effectively across all organizational levels
• Preferred: Certification in quality management (ASQ CQE, CQA, or equivalent)
• Preferred: Certification ISO 9001:2015 (Lead Auditor)
• Preferred: Experience in regulated industries such as aerospace, automotive, medical devices, or pharmaceuticals

Additional Information

** Equal Opportunity Employer, including disability / veterans**

*Bosch adheres to Federal, State, and Local laws regarding drug-testing. Employment is contingent upon the successful completion of a drug screen and background check. Candidates who have been offered the position must pass both screenings before their start date.

Your well-being matters at Bosch! We offer a competitive compensation and a benefits package designed to empower you in every area of your life. This includes premium health coverage, a 401(k) with generous matching, resources for financial planning and goal setting, ample paid time off, parental leave, and comprehensive life and disability protection. We're investing in your success!

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