Sr Quality Engineer Department: QualityLocation: Sturtevant, WISTART YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?reqid=3222501&source=3222501-CJB-0) About us:For over three decades, Cirtec Medical has been a leading provider of manufacturing solutions for complex Class II and III medical devices. We specialize in providing comprehensive services from design and development to manufacturing and finished device assembly. Our expertise spans active implants and neuromodulation, interventional cardiology, structural heart, minimally invasive surgical systems, smart orthopedics, and precision components.Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenge, you may be a perfect fit for our team!Position SummaryThe Senior Quality Engineer will develop, establish, and maintain quality engineering methodologies, systems and practices which meet customer and regulatory requirements. This role will be focused on providing quality engineering support to the new product development process, operations/production, and quality systems. This individual will also serve as a Quality representative to improve awareness, visibility, and communication on quality initiatives to support site and corporate quality goals and priorities.Key Responsibilities
Provide Quality Engineering support for engineering product development, or sustained manufacturing.
Provide Quality Project Management support as needed for product transfers from development to validation to production.
Verification/Validation System Owner responsible for the development and management of the verification/validation master plan along with the verification/validation determination.
Develop and maintain Standard Operating Procedures.
Develop and maintain project Quality Plans for assigned projects.
Develop protocols, perform statistical analyses, and write reports for validations and formal product/process development, which requires quality-engineering involvement.
Support the development and implementation of IQ (Installation Qualification) and OQ (Operational Qualification) protocols to ensure compliance with the Quality System.
Provide Quality Engineering support for engineering/manufacturing.
CAPA (Corrective and Preventative Action) system owner or support responsible for the support of the corrective action system and procedures.
Interact with customers and suppliers to resolve CAPA and complaint investigations.
Provide Quality Support for the disposition of material via NCRs.
Support supplier quality activities including vendor approval and maintaining and assessing vendor performance data (i.e. SCAR/on time).
Review and document procedure changes for quality requirements and compliance with the quality system.
Develop quality systems and procedures as needed.
Audit support for third party audits, customer audits and internal audits.
Support the implementation of continuous improvement initiatives.
Develop and maintain production quality control plans.
Initiate and maintain SPC (Statistical Process Control) for production processes.
Lead or support FMEA (Failure Modes & Effects Analysis), and DOE (Design of Experiment) as applicable.
May serve as backup to Quality Manager.
Complies with company, quality, and safety standards, policies, and procedures.
Other duties as assigned.
This is not a remote position.Must Have:
A Bachelor-s degree (STEM engineering discipline preferred) and 5 years of experience required; or a combination of education and relevant work experience.
Experience in an engineering environment with mechanical, tool design, and manufacturing processes (medical device preferred).
Must be fluent in use of computer systems for the analysis of data, specifically Microsoft Office.
Must possess excellent verbal communication, organizational and management skills.
Training or equivalent experience in computer use and software-Microsoft Word, Excel, Power Point and Access. Minitab experience desirable.
Must be able to read, write and speak fluent English.
Must be able to implement quality programs, interpret the collected data, and present the data to management to drive continuous improvement.
Must be able to analyze and process information; promote Process Improvement, Developing Standards, Managing Processes, Manufacturing Methods, and Procedures; and Supports Innovation.
Salary Range$95,000 - $115,000Company StatementCirtec Medical Corporation considers everyone for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all its related companies fully endorse equal opportunity. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec-s goal to create an enjoyable work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every stage of your career and life. Our benefits include training and career development, healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.START YOUR APPLICATION (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?reqid=3222501&source=3222501-CJB-0)