Quality Engineer

DiaSorin; Stillwater (MN); On-site; USD 75,000 - 93,000; Full time

Job summary

DiaSorin Inc in Stillwater, MN seeks a Quality Engineer to serve as a QA expert in process controls, validation, CAPA and risk management. You will partner with manufacturing, supply chain and development to ensure compliant product quality and robust processes.

The role emphasizes Design Control, MDR/IVDR readiness, data analysis and internal/external audits, with a focus on continuous improvement and Lean initiatives across the QMS.

Qualifications

• Bachelor's Degree in Engineering, Life Sciences or related field.
• 3+ years quality engineer experience in medical device or regulated industry.
• FDA QSR and ISO 13485, 9001 & 14971 and MDSAP Compliance.
• CAPA and Root Cause Analysis.
• Quality Auditing and Change Control.
• Design and New Product Development and Process Validation.

Responsibilities

• Provide QA representation and advisement within cross-functional teams.
• Lead CAPA, NCR and risk management activities.
• Review design controls and development processes for compliance.
• Support internal and external audits of the QMS.
• Drive continual improvement of product quality and processes.

Skills

CAPA

Root Cause Analysis

Regulatory compliance

Statistics

Process Validation

Design Control

QMS software

MS Word

PowerPoint

Six Sigma

Education

Bachelor's Degree in Engineering / Life Sciences

Tools

MS Word

PowerPoint

Excel

QMS software

Job description

Quality Engineer

Published on: Aug 24, 2026

Country: United States

Location: Stillwater, Minnesota

Company: DiaSorin Inc

Job Category: Quality

Employment type: Regular Full Time

Req ID: 7837

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

• Build What Matters – Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
• Innovate with Agility at a Global Scale – Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
• Grow in a People-Centered Culture – Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

As a member of the Product Quality Assurance Engineering team, this role will serve as a subject matter expert and go-to authority, regarding best Quality practices and ensuring all Product Quality related activities are performed in a complaint manner to support business objectives. In addition, as a member of the Product Quality Assurance Engineering team, this role will be responsible for serving as an internal consultant on the following activities: Process Controls, Equipment and Process Validation, Non-conforming Product, Risk Management, new Product Development, CAPA, Design/Change Control and Statistical Methods.

Job Responsibilities and Duties

• Provide QA representation, support and advisement within cross-functional teams relating to (but not limited to):
• Non-conforming product
• CAPA
• Process and Material Validation
• Change Management
• Design Control and new Product Development
• Supplier quality and manufacturing issues
• Corporate and local quality plans/projects
• Continual improvement of the QMS and product quality
• Operational Excellence and Lean projects
• Risk Management
• Support the NCR (Non-Conformance) system – review and approve issues, make recommendations, monitor efficacy through key NCR process metrics and help to support and drive the success of metrics
• Ensure procedures are established and accurate to support new Product Development, Product Design Transfer and manufacturing process
• Review design and development processes, ensuring appropriate documentation is established in accordance with the Design Control procedures
• Review manufacturing and product development validation activities to ensure that they are well established, risk-based and compliant with applicable regulations.
• Review, approve and provide recommendations on Change Requests.
• Gather, analyze and report data reflecting status of product and process and provide recommendations to improve such activities
• Use statistical tools to analyze data to make acceptance decisions and improve processes and product
• Review and approve equipment and process validation protocols/reports
• Recommend methods, techniques and principles to ensure compliance, safety, efficacy and efficiency
• Work with manufacturing and supply chain to resolve supply issues of critical components, sub-systems and finished product to ensure that all changes are appropriately validated
• Initiate, investigate, own, drive and/or participate in NC and CAPA issues as needed
• Analyze and translate technical data
• Participate on internal audit team and support external audits
• Perform other duties as assigned.

Education, Experience and Qualifications

• Bachelor's Degree in Engineering, Life Sciences or related field, or equivalent experience required or

• 3+ Years years of quality engineer experience in medical device or other regulated industry
• FDA QSR and ISO 13485, 9001 & 14971 and MDSAP Compliance
• CAPA and Root Cause Analysis
• Quality Auditing (both in performing internal audits and participating in external audits)
• Document and Change Control
• Nonconformance Process
• Design and New Product Development
• Process Validation methodology
• Risk Management and usage of PFMEA templates
• Statistical methods (process capability, hypothesis testing, regression/correlation, SPC, DOE)
• Computer skills and software knowledge – MS Word, PPT and Excel
• Immunochemistry/immunoassay
• Six Sigma methodology
• IVDR or MDR
• Software Validation and Data Integrity
• Working knowledge of statistical methods
• Usage of a QMS software system
• required

What we offer

The hiring range for this position is $74,800 - $93,400 annually. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.

Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact [e-mail].

Recruitment Fraud Notice

Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact [e-mail] for verification.

Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.