Manufacturing Quality Engineer

The Quality Engineer will be responsible for ensuring that all products meet the highest quality standards in compliance with customer specifications, industry regulations, and company requirements. This role involves the assessment, analysis, and continuous improvement of manufacturing processes to ensure the consistent production of high-quality components. RESPONSIBILITIES Monitor and evaluate manufacturing processes to ensure compliance with quality standards and regulatory requirements. Conduct inspections, audits, and tests of components. Analyze and resolve quality issues, implementing corrective and preventive actions as necessary. Develop, implement, and maintain standard operating procedures (SOPs) for quality control and testing. Review product designs, specifications, and production methods to ensure quality standards are integrated from the beginning. Work with engineering and production teams to optimize production methods and quality standards. Conduct root cause analysis of quality problems and collaborate with cross‑functional teams to resolve issues. Collaborate with clients and external partners to ensure product quality and resolve quality concerns promptly. Supervise and mentor quality technicians, providing guidance on testing, inspections, and reporting. Develop and deliver training programs to educate production staff and quality technicians on quality standards and best practices. Maintain detailed records of inspections, tests, and audits to ensure traceability and compliance with industry standards. Prepare and present quality reports to management, highlighting key performance indicators (KPIs), trends, and improvement initiatives. QUALIFICATIONS Bachelor’s degree in Mechanical Engineering, Industrial Engineering, Quality Engineering, or a related field. Minimum of 4‑8 years of experience in a quality engineering role, ideally within the HVAC, thermal systems, or assembly component industries. Experience in supervising quality technicians and leading quality improvement initiatives. Knowledge of quality standards such as ISO 9001, ASQ certifications, and other relevant industry standards. Experience with statistical analysis, process control techniques, and root cause analysis methods. PHYSICAL & ENVIRONMENTAL DEMANDS The role is primarily based in a manufacturing facility, requiring regular site visits and interaction with production teams. Required to wear personal protective equipment (PPE) and adhere to safety protocols. The role involves extended periods of sitting in front of a computer. Occasional standing or walking may be required during meetings, presentations, or site visits. Work is primarily conducted in an office environment with controlled temperature and lighting. TIME TRAVEL REQUIRED Travel to different office or plant locations, client sites, or conferences may be necessary. About the Team Work Authorization No calls or agencies please. Vertiv will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F‑1, H‑1, H‑2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire. Equal Opportunity Employer We promote equal opportunities for all with respect to hiring, terms of employment, mobility, training, compensation, and occupational health, without discrimination as to age, race, color, religion, creed, sex, pregnancy status (including childbirth, breastfeeding, or related medical conditions), marital status, sexual orientation, gender identity / expression (including transgender status or sexual stereotypes), genetic information, citizenship status, national origin, protected veteran status, political affiliation, or disability. #J-18808-Ljbffr