Quality Engineer 3, Design Assurance
Teleflex · Maple Grove, MN
- Level
- Engineer
- Team
- Quality
- Travel
- 10%
- Experience asked
- 5+ years
- Industry
- Medical devices
- Posted
- Recently
The role in 30 seconds
An engineer-level quality role at Teleflex (medical devices) in Maple Grove, MN. The Quality Engineer III, Design Assurance is responsible for quality throughout new product development and improvement up to and including technology transfer and commercialization.
- They ask for
- 5+ years
- Tools it names
- Root cause, Control plans, MSA / Gage R&R, CAPA, Validation (IQ/OQ/PQ), Supplier quality
- Day to day
- about 10% travel
Read from the posting. The full description is below.
From the plant jobs report · week of October 19, 2026
Quality Engineer roles in Minnesota: typical posted base $83k–$141k.
Median of the low and high ends of 33 live postings that list pay, out of 56 quality engineer openings in Minnesota, read from manufacturers' own careers sites.
Minnesota plant jobs report →Pay by team and state →What moves pay →
How this role compares
Against 55 other live quality postings in Minnesota.
- Base pay
- Not listed in this posting
- Experience asked
- Typical (5+ years)
Typical $83k–$135k, from 31 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- ✓ Root cause 57%
- ✓ Validation (IQ/OQ/PQ) 43%
- Lean 41%
- Six Sigma 41%
- ✓ Supplier quality 39%
- ✓ CAPA 38%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Teleflex
Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- The posting says about 10% travel. Between which sites?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
Full description from TeleflexAs posted on their careers site.ShowHide
Position Summary
As a member of a cross-functional team, the Quality Engineer III, Design Assurance is responsible for quality throughout new product development and improvement up to and including technology transfer and commercialization. The Quality Engineer III, Design Assurance ensures that applicable elements of the Quality System and external standards are followed. As the voice of Quality, the Quality Engineer III, 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
- ◆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.
- ◆Analyze post-market surveillance data periodically throughout a product’s lifecycle to feed back into it’s risk file in order to reflect it's current risk profile. Support Clinical and Medical Writers in the analysis of available clinical data, as required.
- ◆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 product’s 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.
- ✓Support development and validation of 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. Accountable for CAPA requirements, timeliness, and effectiveness; present phase status (progress, risks, escalations, and resource needs) at CRB/ECRB meetings; review and disposition CAPA phase, extension, and support technical reviews as needed.
- ✓Support Regulatory Affairs with relevant submissions, approvals, requests, and inquiries.
- ✓Define, identify, and apply product and process control methods such as developing control plans, identifying essential design outputs and critical control points, and developing and validating work instructions.
- ✓Apply the concepts of producer and consumer risk and related terms, including operating characteristic curves, AQL, LTPD, AOQ, AOQL, etc. Interpret and select variable, attribute, and zero-defect sampling plans.
- ✓Apply supplier management principles and provide input on projects for supplier selection, quality expectation letters, supplier quality agreements, and process qualifications.
- ✓Partner with PMO to apply project management tools in order to define project deliverables and establish a project schedule.
- ✓Contribute to corporate technical programs (e.g., system improvement, remediation, harmonization) in areas related to those identified in this position description.
- ✓Generally apply the above concepts as required at the local, regional, and departmental level.
Requirements
- ✓B.A. or B.S. degree i
Show full description ↓Show less ↑
Expected Travel : Up to 10%
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s 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 teleflex.com .
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.
More Quality roles nearby
- Principal Quality Engineer - Program Quality · BAE Systems · Maple Grove
- Principal Quality Engineer – Design & Operations Quality · BAE Systems · Maple Grove
- Engineer Quality II – Procurement Quality Support Engineering / Calibration · BAE Systems · Maple Grove
- Senior Quality Systems Engineer · Boston Scientific · Maple Grove
