Manufacturing quality engineering

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. This position is primarily responsible for monitoring and auditing the quality of all manufactured goods in a medical device industry. Interact with customers and suppliers in support of engineering projects.

Provide Quality Engineering support for engineering project development, or sustained manufacturing.

Provide Quality Project Management support as needed for product transfers from development to validation.

Develop and maintain project Quality Plan for assigned projects.

Develop protocols, perform statistical analyses, and write reports for validations and formal process development, which requires quality-engineering involvement such as DOEs.

Support the development and implementation of IQ (Installation Qualification) and OQ (Operational Qualification) protocols to ensure compliance with the Quality System.

Support Risk Management activities for New Product Development (NPD) programs within our Precision Component Business

Provide Quality Engineering support for manufacturing.

Interact with customers and suppliers to resolve CAPA and complaint investigations and in support of manufacturing.

Provide Quality Support for the disposition of material via NCR's.

Provide Quality Project Management Support as needed for product transfers from validation to production.

Vendor approval and maintain and assess vendor performance data (i.e. 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 for production processes.

Develop and maintain production quality control plans.

Initiate and maintain SPC (Statistical Process Control) for production processes.

Provide initiative and support for FMECA (Failure Modes & Effects Criticality Analysis), and DOE (Design of Experiment as applicable.

A Bachelor's degree in a STEM engineering discipline

2+ years of experience in Quality Engineering required

Experience in an engineering environment with mechanical, tool design, and manufacturing processes (medical device preferred)

Analyze and process Information, Promote Process Improvement, Developing Standards, Managing Processes, Manufacturing Methods and Procedures, Supports Innovation.

Must be fluent in use of computer systems for the analysis of data, specifically Microsoft Office.

Training or equivalent experience in computer use and software-Microsoft Word, Excel, Power Point and Access.

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.

Cirtec Medical Corporation considers 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 of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

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.

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