Quality Manager

Job Title: Quality ManagerLocation: San Carlos, California Job Type: Full-Time | On-SiteAdvantage Converting is a dynamic and fast-paced manufacturing company with over 30 years of experience delivering high-quality components and engineered solutions to medical, electronics, green energy, and industrial markets. We are a team of creative thinkers and problem solvers"”and we're looking for a Quality Manager to lead and elevate our Quality function.Position SummaryAs the Quality Manager, you will lead all aspects of our Quality processes and systems. This is a key leadership position responsible for managing the Quality Management System (QMS), internal and external audits, regulatory and safety compliance, and leading a team of Quality Technicians. You will collaborate with cross-functional teams to drive continuous improvement, ensure product integrity, and exceed customer expectations.Key ResponsibilitiesOversee and maintain the QMS in compliance with ISO 13485 and customer requirementsLead internal and external audits (customer, supplier, registrar) and report results to the Executive TeamSupervise Quality Technicians responsible for First Article, In-Process, and Final InspectionsManage supplier quality performance, including evaluations, audits, and non-conformance resolutionDrive Root Cause Analysis and Corrective & Preventive Actions (CAPA) for internal and external issuesManage customer complaints, investigate issues, and coordinate resolutionsServe as the primary point of contact for all quality-related communications with customers and suppliersEvaluate current quality team structure and staffing; build and develop a high-performing quality team to support business needsMaintain and manage clean room quality and testing protocolsOversee equipment qualifications and Process ValidationsPartner with leadership to define and implement quality strategies and KPIsFacilitate cross-departmental collaboration to implement process improvementsResearch and implement best practices, technologies, and systems to improve quality and complianceMitigate operational risks related to manufacturing, safety, and deliveryManage Safety and IIPP (Injury and Illness Prevention Program) complianceDevelop and enforce Standard Operating Procedures (SOPs) for manufacturingLead quality and safety-related employee training programsPerform other duties as needed to support operational excellenceQualificationsEducation & Experience:Bachelor's degree in manufacturing, engineering, medical device, or related field4+ years in a Quality leadership role within a manufacturing environment3+ years managing ISO 13485 QMS and leading customer/supplier auditsProven experience with precision component manufacturing and contract manufacturing environmentsHands-on experience with CAPA, root cause investigations, and quality metricsProficient in interpreting engineering drawings and using inspection equipmentStrong organization and communication skills; experience delivering trainingComfortable working independently and leading small teamsMust be available for full-time, on-site work in San Carlos, CAPreferred:Familiarity with medical device manufacturing and regulated industriesSpanish-speaking abilityCompensation & BenefitsCompensation & BenefitsSalary: $110,000 - $140,000 per year Benefits Include:401(k) with employer matchMedical, dental, and vision insurancePaid vacation, holidays, and sick timeSupportive team environment with opportunities for growthAdditional DetailsSchedule:Monday-Friday, 8-hour shifts% time spent on the manufacturing floor (TBD)Work Location:San Carlos, CA 94070 (In-person role)Applicants must be able to relocate before starting workReady to make a meaningful impact in a growing company? Apply now and become part of the Advantage Converting team.

Created: 2025-10-02