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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 solversand were 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:
- Bachelors 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:
- MondayFriday, 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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