Quality Manager

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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

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