Advantage Converting
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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
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
Schedule:
Monday–Friday, 8-hour shifts
% time spent on the manufacturing floor (TBD)
Work Location:
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.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Quality Assurance Industries Medical Device Referrals increase your chances of interviewing at Advantage Converting by 2x Get notified about new Quality Assurance Manager jobs in
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Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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