Quality Engineer 2, Design Assurance PMS

Expected Travel : Up to 10%

Requisition ID : 12990

About Teleflex Incorporated

As a global provider of medical technologies Teleflex is driven by our purpose to improve the health and quality of peoples lives. Through our vision to become the most trusted partner in healthcare we offer a diverse portfolio with solutions in the therapy areas of anesthesia emergency medicine interventional cardiology and radiology surgical vascular access and urology. We believe that the potential of great people purpose-driven innovation and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow Barrigel Deknatel LMA Pilling QuikClot Rüsch UroLift and Weck trusted brands united by a common sense of purpose.

At Teleflex we are empowering the future of healthcare. For more information please visit .

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients lives.

Position Summary

As a member of a cross-functional team the Quality Engineer II Design Assurance is responsible for quality throughout new product development (up to and including design transfer and commercialization) and sustaining projects. The Quality Engineer II Design Assurance ensures that applicable elements of the Quality System and external standards are followed. As the voice of Quality the Quality Engineer II Design Assurance applies best-practice quality team-based and statistical tools and techniques and promotes the value and use of such tools throughout the organization.

Principal Responsibilities

Author and maintain post-market periodic safety update reports for Teleflex devices.

Interface with key functional areas within Teleflex to obtain necessary information and documents required for the development and maintenance of post market documentation.

Apply technical solutions to improve problem solving data collection and analysis to add efficiency and effectiveness to the post market process and the use of post market data in the ongoing risk management activities for supported products

Partner with R&D Marketing Regulatory Affairs and Operations to support activities in product and process design such as design verification design validation design reviews design transfer and all other aspects of a design history file.

Create and maintain risk files consisting of but not limited to risk management plans hazard and risk analyses failure mode and effects analyses and risk management reports to assess the risks associated with a product.

Use appropriate quality tools and statistical techniques to collect and summarize data draw conclusions with confidence determine sample sizes apply data distributions identify relationships between variables calculate reliability design and analyze experiments determine process and performance capability and make statistically supported decisions.

Apply the most relevant and useful quality philosophies throughout Design Control and its related processes for both new product development and sustaining. Understand and manage work to minimize cost of quality throughout the products lifecycle.

Ensure compliance of all practices to the Quality Management System. Ensure comprehensive documentation is available adequate records are produced and change management is implemented.

Interpret customer feedback to define user needs and product requirements as part of a cross-functional team.

Partner with Product Quality Assurance and Operations to make risk-based decisions associated with nonconformances and technical complaints.

Understand applicable external regulations and internal standards that drive compliance and apply them in their daily function. Perform audits of Design History Files and support both internal and external audits.

Partner with Human Factors SMEs and R&D to assess the usability of a device throughout design and development.

Develop and validate test methods. Identify and apply metrology techniques such as calibration systems traceability measurement error and control of standards and devices. Conduct measurement system error studies such as Gage R&R.

Perform root cause analysis of identified issues and identify appropriate corrective and preventive action. Use the NC and CAPA systems as needed to structure activities.

Support Regulatory Affairs with relevant submissions approvals requests and inquiries.

Partner with PMO to apply project management tools in order to define project deliverables and establish a project schedule.

Education / Experience Requirements

B.A. or B.S. degree in a technical discipline such as engineering or science (equivalent experience may be considered).

2 to 5 years of quality engineering or design assurance experience (preferably in the medical device industry).

Specialized Skills / Other Requirements

ASQ certification preferred (e.g. CQE CQA CMDA CRE CSSGB / CSSBB).

Basic understanding of industry regulations such as ISO 13485 ISO 14971 and FDA 21CFR820.

Proficient in MS Office and Minitab or other statistical softwares.

Strong organizational and time management skills to meet deadlines while managing multiple projects.

Strong analytical and critical thinking skills.

Proficient in technical report writing and review.

Strong verbal and written communication skills.

Foster a positive culture of growth collaboration and achievement across the organization.

The pay range for this position at commencement of employment is expected to be between $75100.00 to $112700.00 however base pay offered may vary depending on multiple individualized factors including market location job-related knowledge skills and experience. The total compensation package for this position will also include benefits such as medical prescription drug dental and vision insurance flexible spending accounts participation in 401(k) savings plan and various paid time off benefits such as PTO short- and long-term disability and parental leave dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired employee will be in an at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time including for reasons related to individual performance Company or individual department / team performance and market factors.

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At Teleflex we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age race religion color national origin ancestry sexual orientation disability nationality sex or veteran status. If you require accommodation to apply for a position please contact us at : or

Teleflex the Teleflex logo Arrow Barrigel Deknatel LMA Pilling QuikClot Rüsch UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates in the U.S. and / or other countries.

2025 Teleflex Incorporated. All rights reserved.

Key Skills

Test Cases,Performance Testing,Quality Assurance,SOC,Agile,Debugging,Jira,Perl,Software Testing,Test Automation,Scripting,Selenium

Employment Type : Full Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 75100 - 112700