Supplier Quality Engineer

Supplier Quality EngineerThe Supplier Quality Engineer collaborates with suppliers, manufacturing, development, and supply chain teams to ensure suppliers are qualified and deliver high-quality components. This role involves monitoring suppliers, investigating nonconformances in supplied components, implementing corrective actions, and driving continuous improvement. Additional responsibilities include conducting supplier assessments and audits, maintaining compliant documentation, and ensuring adherence to FDA 21 CFR Part 820 and ISO standards.Responsibilities:Collaborate with suppliers through meetings, audits, and reviews to identify risks, drive corrective actions, and improve quality outcomes.Plan and lead supplier audits to maintain compliance with applicable standards.Lead First Article Inspection and/or Component Qualifications.Investigate and resolve supplier-related non-conformance material reports (NCMRs) that impact product quality, manufacturing, or business performance.Drive improvement and corrective action (SCARs) for components sourced from suppliers.Analyze incoming material defects and communicate issues to suppliers.Develop, maintain, and improve receiving inspection and process documentation to ensure consistency and compliance.Generate and maintain incoming inspection procedures.Assist in generating component specifications.Complete supplier assessments and evaluations.Evaluate and support supplier changes for potential effects on design, quality, and regulatory compliance for manufacturing and development projects.Participate in risk management activities such as FMEA development and updates.Track purchased item requirements back to design requirements.Evaluate and facilitate supplier process validation.Essential Skills:4+ years of experience in supplier quality, specifically in a medical device environment (ISO13485).Extensive expertise in supplier management and quality systems.Experience in vendor management, supplier relationship, and performance.Understanding of ISO and FDA QSR requirements including design controls, risk management, and process validation.Proficiency in eQMS systems, preferably GAS.Ability to conduct Root Cause Analysis (RCA) and draw valid conclusions.Highly proficient with MS Office (Word, Excel, Access, and PowerPoint), internet, and email systems.Ability to interpret and understand drawing specifications, tolerances, procedures for inspection, and application of sampling plans.Additional Skills & Qualifications:Auditor certification and experience conducting supplier audits.Automated inspection programming and validation (preferred).Solid understanding of software capabilities and business applications.Familiarity with inspection devices such as pin gauges, micrometers, calipers, pressure gauges, rules, and microscopes.Broad knowledge of theory and principles of statistics.Ability to accurately prioritize and execute tasks with minimal direction.Job Type & Location:This is a Permanent position based out of Minneapolis, MN.Pay and Benefits:The pay range for this position is $95000.00 - $101000.00/yr. Standard Benefits: - 401K - Health, dental, vision - In house gym - HSA options - Yearly bonuses based on company/individual performance - Three weeks PTO (+ week between Christmas and New Years off)Workplace Type:This is a fully onsite position in Minneapolis, MN.Application Deadline:This position is anticipated to close on Aug 19, 2026.About Actalent:Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on click.appcast.io for other accommodation options.San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.