Design Quality Engineer - Maple Grove, MN
Hybrid Schedule
Pay Rate : $45-50+ per hour
Qualifications :
- Bachelor’s degree with 5–8 years of experience, Master’s degree with 3–6 years, or PhD with 0–3 years.
- Experience in design control and risk management of next-generation medical devices.
- Background in pharmaceutical or combination products, with knowledge of 21 CFR 211 and ICH Quality Guidelines.
Responsibilities :
Apply clinical expertise to guide device testing and design decisions.Develop, direct, and execute design control and risk management plans for complex projects, independently or in collaboration with cross-functional teams.Lead the development and implementation of product risk management tools, including Hazard Analysis, Fault Tree Analysis, and FMEAs.Provide quality input as a subject matter expert (SME) and / or independent reviewer at key project milestones (e.g., design reviews, project design plans, design / process changes).Promote and ensure compliance with company quality systems, business processes, health & safety standards, and applicable market / regulatory requirements.Quality & Compliance Expertise :
Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.Demonstrate proficiency in validation and statistical techniques to ensure compliance with regulatory requirements and internal standards.Maintain expertise in pharmaceutical and combination product regulations, including 21 CFR 211 and ICH Quality Guidelines.Stay current with ISO, EN, FDA, MDR, and other product development–related regulatory requirements, and communicate updates to the Product Development team.Culture & Leadership :
Foster a culture of quality-driven, patient-centric product development and customer satisfaction.