A Manufacturing Process Engineer develops workflow, work station, and equipment improvement recommendations within a company's manufacturing environment. Fine tunes manufacturing processes by researching, designing, modifying, and testing manufacturing methods and equipment. Evaluates manufacturing processes, applies knowledge of product design, fabrication, assembly, tooling, and material.
Lead Design Quality Engineer NeuWave Medical, Inc - 3.5 Madison, WI Job Details 22 hours ago Qualifications ISO standards Quality control audit Quality assurance audits Quality risk management Medical device manufacturing facility experience Desktop applications Design controls Biomedical regulatory compliance Productivity software Quality audits FDA regulations Full Job Description Position Summary The Lead Design Quality Engineer owns design-control quality engineering for NeuWave Medical's microwave ablation probe and console portfolio. This role partners with R D and Regulatory Affairs to ensure design inputs, outputs, verification, validation, and design risk management activities meet
FDA QSR, ISO
13485, and EU MDR requirements across new product development and sustaining design changes. Key Responsibilities Own the QA role in design control activities — managing the Design and Development File (DDF), which fulfills the traditional Design History File (DHF) role, across New Product Development (NPD) and sustaining design changes. Maintain the Risk Management Plan, Risk Management Report, and Risk Management File, and facilitate design risk management activities (FMEA, risk analysis) in accordance with
ISO 14971.
Participate on the Design Review Team (DRT), confirming design deliverables are complete, verified, and meet applicable regulatory and quality standards before progressing through phase gates. Ensure design verification and validation testing is conducted per approved plans and results are documented in the DDF. Review and approve engineering change orders affecting device design; identify regulatory requirements and applicable standards across outsourced design activities. Partner with R D, Regulatory Affairs, and Manufacturing Engineering on design transfer and design change control. Support Computer System Validation (CSV) activities for systems supporting design and quality processes. Support internal and external audits related to design controls, including hosting regulatory and Notified Body auditors as needed. Required Qualifications Bachelor's degree in Engineering or a related technical field (or equivalent combination of education and experience). 5+ years of quality engineering experience at a medical device manufacturer, with a focus on design controls and/or NPD. Working knowledge of
ISO 13485, 21 CFR
820, and
ISO 14971.
Demonstrated experience with internal and/or external quality audits. Proficient with standard office software (Microsoft Office suite or equivalent). Preferred Qualifications ASQ certification (CQE, CRE, or equivalent).
ISO 13485
Lead Auditor certification. Experience hosting Notified Body/Registrar auditors or FDA investigators during on-site inspections is a plus. Experience with eQMS platforms, specifically ComplianceQuest, is a plus. Prior CSV/software validation experience. Travel Requirements Less than 10%. Work Environment & Physical Demands Work is primarily performed in an office and light-manufacturing/lab environment at NeuWave Medical's Madison, WI facility. Requires the ability to sit or stand for extended periods, use a computer workstation, and occasionally lift up to 25 lbs. Reasonable accommodations will be made for individuals with disabilities to perform essential job functions. Equal Employment Opportunity NeuWave Medical (a Precision IO Group company) 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, age, disability, protected veteran status, or any other status protected by applicable law.
