Manufacturing Quality Specialist

Manufacturing Quality SpecialistCardioQuip is a dynamic and innovative company specializing in the manufacturing, maintenance, and design of Cardiovascular Operating room technology. This position plays a crucial role in ensuring the functionality and reliability of our products, which are vital for medical applications.Direct Report: Director of ManufacturingWorks regularly with Production, Document Control, and the Director of Quality and Regulatory.ResponsibilitiesOriginates and investigates manufacturing nonconformances per applicable procedures; ensures nonconforming material is properly identified, quarantined, and controlled.Represents Manufacturing on the Material Review Board (MRB), as appointed; supports dispositions, defect coding, trending, and escalation to CAPA or SCAR, as appropriate.Owns manufacturing CAPAs as assigned, from initiation through closure, including root cause investigation, action planning, implementation, and verification of effectiveness.Authors and revises manufacturing and supply chain SOPs and assists with updates to work and assembly instructions through the change order process.Generates, reviews, and uploads Device History Record (OHR) documentation for each device built, in accordance with applicable procedures, ensuring complete traceability.Performs OHR reviews to verify that production documentation is complete, accurate, and appropriately executed prior to final release.Supports receiving inspection dispositions, supplier evaluations, SCAR issuance and tracking, and CAPA-related communication with suppliers and contract manufacturers.Assists the Quality Inspector with inspections on the manufacturing floor, as needed.Supports internal audits and FDA/notified body inspections of manufacturing and supply chain areas and prepares production quality metrics for management review.Performs other duties as assigned.Required Skills/AbilitiesReads and interprets technical drawings, bills of material, and assembly instructions.Applies good documentation practices (GDP) and structured root cause analysis methods.Proficient with Microsoft Office Suite.Strong attention to detail, sound judgment, and clear communication with production teams.Education and ExperienceTwo years of manufacturing or quality experience required; medical device experience preferred.Associate or Bachelor's degree in a technical or quality discipline preferred.Knowledge of ISO 13485:2016, 21 CFR 820 (QMSR), and EU MOR 2017/745 preferred.Hands-on experience with nonconformance, CAPA, and OHR processes strongly preferred.Experience with ERP and electronic document control systems preferred.ASQ CQA, CQE, or CQT certification preferred.Physical RequirementsMust be able to traverse the distribution warehouse and access a variety of storage spaces and shelving units by stretching, squatting, and reaching.Must be able to lift up to 50 pounds at a time.What We OfferCompetitive CompensationA fair salary commensurate with experience and qualifications.Comprehensive BenefitsHealth, dental, and vision insurance.Retirement savings plan with company contribution.Dynamic Work EnvironmentA supportive team culture that values innovation, improvement, and empowerment.Work-Life BalancePaid time off, including vacation days and holidays.Fun and Engaging CultureWe believe in working hard and celebrating our successes together, fostering a sense of camaraderie and enjoyment in our work.Why Join?At CardioQuip, we are dedicated to empowering people towards better healthcare. As a leading company in the medical device industry, we design and manufacture advanced cardiovascular devices that make a real difference in patients' lives. Our humble beginnings started with just two founders in a small office, and we've grown into a dynamic team that values every member's contribution. We believe in fostering an environment where our team is empowered, customer-focused, and continually striving for improvement—all while having fun along the way.