Quality Engineer at Vantedge Medical

Wheeling, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

20 Jul, 26

Salary

95000.0

Posted On

21 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

ISO 13485, Quality Management Systems, Quality Assurance, Root Cause Analysis, Corrective And Preventive Actions, CAPA, Precision Machining, Medical Device Manufacturing, Statistical Analysis, Risk Management, Minitab, SPC, Microsoft 365, Auditing, Supplier Quality Management, Regulatory Compliance

Industry

Medical Equipment Manufacturing

Description

Description Quality Engineer Full-Time | On-site Exempt | $75k - $95k *We are not accepting candidates from third party agencies. About Us: Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do – and have a lot of fun doing it. About the Role: We are seeking a skilled Quality Engineer with a strong background in ISO 13485 to join our team. The ideal candidate will have experience in quality management systems within the precision machining sector, with a particular focus on medical device manufacturing. This role will be critical in ensuring our products meet the stringent quality standards required for regulatory compliance and customer satisfaction Responsibilities: Quality Management Systems: Develop, implement, and maintain quality management systems in accordance with ISO 13485 standards. Ensure compliance with regulatory requirements and industry best practices. Quality Assurance: Oversee quality assurance activities including the creation and management of inspection plans, control plans, and documentation procedures. Conduct audits, inspections, and tests to verify product quality. Continuous Improvement: Drive continuous improvement initiatives within the quality management system. Identify areas for improvement, recommend changes, and lead efforts to enhance product quality and operational efficiency. Non-Conformance Management: Investigate and manage non-conformances, including root cause analysis and corrective action planning. Ensure timely resolution and implementation of corrective and preventive actions (CAPA). Documentation: Ensure all quality documentation, including work instructions, standard operating procedures (SOPs), and records, are accurate, up-to-date, and compliant with ISO 13485 and other relevant standards. Training and Support: Provide training and support to production and engineering teams on quality standards, processes, and best practices. Foster a culture of quality awareness and responsibility across the organization. Supplier Quality Management: Assess and manage supplier quality performance. Collaborate with suppliers to resolve quality issues and ensure the quality of incoming materials and components. Regulatory Compliance: Stay current with regulatory requirements and industry standards related to precision machining and medical device manufacturing. Ensure that the company’s practices are compliant with relevant regulations. Other duties as assigned Requirements Education: Bachelor’s degree in engineering, Quality Assurance, or a related field preferred. Relevant certifications (e.g., CQE, Six Sigma) are a plus. Experience: Minimum of 5 years of experience in a quality engineering role, preferably within the precision machining or medical device industry. Demonstrated expertise in ISO 13485 is highly preferred. Skills: Strong knowledge of ISO 13485 standards and quality management principles. Experience with risk management, statistical analysis, and root cause analysis techniques. Proficiency in quality tools and software (e.g., Minitab, SPC). Proficiency in Microsoft 365 (Outlook, Word, Excel, PowerPoint, SharePoint, etc.). Language: Fluent in English. Other: Strong analytical and problem-solving skills, attention to detail, and the ability to work effectively in a fast-paced, collaborative environment.

Responsibilities

The Quality Engineer will develop and maintain quality management systems in compliance with ISO 13485 standards while overseeing quality assurance and continuous improvement initiatives. They are also responsible for managing non-conformances, conducting root cause analysis, and ensuring regulatory compliance across manufacturing processes.