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Sr. Design Quality EngineerAvalign Technologies, Inc. • Schaumburg, Illinois, United States
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Sr. Design Quality Engineer

Avalign Technologies, Inc.
  • US
    Schaumburg, Illinois, United States
  • US
    Schaumburg, Illinois, United States
Jetzt Bewerben

Über

Posted Tuesday, June 23, 2026 at 4:00 AM
Avalign produces innovative, high-performance, and cost-effective medical devices with a particular focus on high growth and ingenuity. Our team is growing quickly and proud of the fact that our custom-made devices continue to make a huge difference in the lives of medical professionals and their patients. Our employees are actively involved in the design, engineering and manufacture of technologically advanced medical devices that ensure that we meet our customer’s quality specifications for each product we produce.
The Design Quality Engineer will be responsible for the quality and regulatory related activities associated with new product development. New product development activities will occur in the contract development context and in the specification developer context. These activities span all aspects of the new product development process. The Design Quality Engineer will advise customers in the contract development context how to incorporate Critical-To-Quality (CTQ) and Design-For-Inspection (DFI) into the development process. The Design Quality Engineer will provide CTQ and DFI input internally while ensuring that Avalign specification development activities conducted by Research and Development (R&D) comply with associated policies, procedures and work instructions as outlined in the design control elements of the Quality Management System (QMS).
The Design Quality Engineer will be responsible to ensure that regulatory compliant technical documentation is compiled and for ensuring the ongoing compliance of the technical documentation for assigned Avalign Technologies design owned products. The Design Quality Engineer will assist in regulatory filings for Avalign Technologies design owned products whether this includes Avalign filing, supporting the customer to file, or a third party filing the regulatory submission.
A working knowledge of related global design regulations is required. (ISO 13485, ISO 14971, 21 CFR Part 820, and, preferably, EU Medical Device Regulation) The position requires a hands‑on self‑directed style, and the ability to influence and effectively communicate vertically, horizontally, across functions, externally with customers and internally with co‑workers. The ideal candidate must demonstrate ability to self‑direct, strong analytical abilities, and strong verbal and written communication skills. The position reports directly to the Director of Regulatory Affairs.
What You Will Do:
Responsible for supporting a design control quality system that is complaint to ISO 13485 (latest revision), the Medical Device Directives (while active), and the EU Medical Device Regulations (MDR).
Supports, reviews, and approves the following activities associated with new product development: identification and documentation of user needs, design inputs, outputs, verification, validation, risk assessment, and design change activities to demonstrate new product designs are supported by objective evidence in the design history file prior to product launch.
Participate in supply chain development through Avalign division and external supplier selection and qualification with the new product development team.
Participates in design reviews as required by the design control and development processes.
Serve as GD&T expert for contract developer and specification developer activities.
Assist project managers with design transfer planning and execution including advising on Avalign and vendor manufacturing process validations to support new product development.
Support processes for Medical Device Reporting and Complaints for Avalign as specification developer products.
Ensure required design documentation is retained in design history files and technical files to support regulatory submissions and audits.
Support and maintain all regulatory filings for all Avalign Technologies design owned products whether this includes Avalign filing, supporting the customer to file, or a third party filing the regulatory submission.
Perform corporate internal audits, either as a supporting auditor or as the lead auditor.
Participate in external audits.
Conduct post market surveillance for contract development and specification developer products.
Ensure post launch product design file updates are completed following design change and post market surveillance activities.
Write or update standard operating procedures, work instructions, or policies.
Prepare responses to customer requests for information, such as product data, written regulatory affairs statements, surveys, or questionnaires.
Assist in investigations of product complaints, root cause analysis, corrective action, trending and make recommendations regarding their reportability.
Investigate and complete records related to assigned Nonconformances and CAPAs.
Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or other compliance issues.
What You Will Need:
Bachelor degree or equivalent experience in an engineering or scientific field
5+ years of experience in quality and/or engineering role
2+ years of experience in medical device industry, preferred
2+ years of experience in quality within design control activities supporting new product development, preferred
Experience with ISO 13485, FDA 21 CFR 820 Quality System Regulation, ISO 14971, MDR, or associated regulations.
Ability to travel up to 25%
Preferred Qualifications
Expertise in project management and problem solving skills, including the ability to identify, investigate and resolve technical and/or systemic issues.
High attention to detail and persistence in resolving discrepancies
Excellent interpersonal communication (written and verbal) skills and ability to communicate at all levels of the organization and with suppliers and customers
Familiarity with Quality System Management software
Familiarity with regulatory submissions including:
Coordinating efforts associated with the preparation of regulatory documents or submissions.
Preparation or review of regulatory submissions for domestic or international projects.
What You Won’t Do:
Feel stuck – we offer great opportunities to advance and learn
Get bored – we make a high variety of products, so no day is the same
Feel like a number – we’re a close-knit bunch and always have each other’s backs
Who You Are:
A self-starter who thrives in a fast-paced environment
A quick learner who is always ready to gain depth of knowledge in manufacturing processes
A reliable individual who knows the importance of showing up when it counts
Someone who accept assignments with an open, cooperative, positive and team-oriented approach
Someone who is able to plan and execute plans across teams
An effective communicator, both written and verbal
What You’ll Enjoy:
Competitive compensation and benefits package
Comprehensive medical, dental, and vision insurance
Paid vacation and 10 observed paid holidays per year
Employer funded Basic Life and AD&D insurance
Employer funded STD and LTD insurance
Great 401(k) with company match
Working for a thriving, performance-based company that values promoting from within and career advancement
Temperature controlled environment
Community involvement investing and giving back to the community
Additional free resources such as travel assistance, EAP, etc.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, national origin, gender identity, sexual orientation, age, marital status, veteran status, or disability status. We are an employer that participates in E-Verify and will provide the federal government with your Form I‑9 information to confirm that you are authorized to work in the U.S.
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  • Schaumburg, Illinois, United States

Sprachkenntnisse

  • English
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