Quality Manager

Job Title: Quality Manager Location: San Carlos, California Job Type: Full-Time | On-Site Advantage 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 Summary As 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 Responsibilities Oversee and maintain the QMS in compliance with ISO 13485 and customer requirements Lead internal and external audits (customer, supplier, registrar) and report results to the Executive Team Supervise Quality Technicians responsible for First Article, In-Process, and Final Inspections Manage supplier quality performance, including evaluations, audits, and non-conformance resolution Drive Root Cause Analysis and Corrective & Preventive Actions (CAPA) for internal and external issues Manage customer complaints, investigate issues, and coordinate resolutions Serve as the primary point of contact for all quality-related communications with customers and suppliers Evaluate current quality team structure and staffing; build and develop a high-performing quality team to support business needs Maintain and manage clean room quality and testing protocols Oversee equipment qualifications and Process Validations Partner with leadership to define and implement quality strategies and KPIs Facilitate cross-departmental collaboration to implement process improvements Research and implement best practices, technologies, and systems to improve quality and compliance Mitigate operational risks related to manufacturing, safety, and delivery Manage Safety and IIPP (Injury and Illness Prevention Program) compliance Develop and enforce Standard Operating Procedures (SOPs) for manufacturing Lead quality and safety-related employee training programs Perform other duties as needed to support operational excellence Qualifications Education & Experience: Bachelor’s degree in manufacturing, engineering, medical device, or related field 4+ years in a Quality leadership role within a manufacturing environment 3+ years managing ISO 13485 QMS and leading customer/supplier audits Proven experience with precision component manufacturing and contract manufacturing environments Hands-on experience with CAPA, root cause investigations, and quality metrics Proficient in interpreting engineering drawings and using inspection equipment Strong organization and communication skills; experience delivering training Comfortable working independently and leading small teams Must be available for full-time, on-site work in San Carlos, CA Preferred: Familiarity with medical device manufacturing and regulated industries Spanish-speaking ability Compensation & BenefitsCompensation & Benefits Salary: $110,000 - $140,000 per year Benefits Include: 401(k) with employer match Medical, dental, and vision insurance Paid vacation, holidays, and sick time Supportive team environment with opportunities for growth Additional Details Schedule: 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 work Ready to make a meaningful impact in a growing company? Apply now and become part of the Advantage Converting team.

Created: 2025-10-02