Multi-Site Polymer Quality Manager – ISO/AS9100 Expert

ADDMAN Engineering LLC; Carlsbad (CA); On-site; USD 110,000 - 150,000; Full time

Job summary

ADDMAN Engineering LLC in Carlsbad, CA seeks a Multi-Site Quality Manager to lead the quality program across facilities. You will implement an integrated QMS, drive customer and supplier audits, and improve product and process quality for medical devices.

ITAR compliance and cross-functional collaboration are essential components of this role. The position requires guiding quality strategies, leading investigations, and maintaining data-driven KPI reporting to senior management.

Qualifications

• Bachelor's degree in industrial management, quality management or related field.
• Three to five years related experience and/or training; or equivalent combination.
• Experience with ISO and/or AS9100 quality systems, quality planning and inspection.
• ASQ or similar professional certification preferred.
• Experience with supplier certification and supplier quality planning.

Responsibilities

• Plan, implement, and direct quality programs aligned with ISO/AS9100.
• Maintain quality objectives and communicate them across teams.
• Lead internal, supplier, and customer audits and resolve non-conformances.
• Investigate customer complaints and ensure timely corrective actions.
• Lead root cause analyses and preventive actions on quality issues.
• Oversee supplier evaluation processes and supplier quality concerns.
• Manage quality data, documentation, and KPI reporting.
• Serve as ISO liaison and support ITAR compliance as needed.
• Promote a positive, professional working environment.

Skills

Quality management

ISO AS9100

Auditing

Root cause analysis

Six Sigma

Leadership

Risk management

Problem solving

Cross-functional collaboration

Communication skills

Education

Bachelor's degree in industrial management or quality management

Tools

Global Shop Solutions

PC DMIS

ERP systems

Job description

ADDMAN Engineering LLC in Carlsbad, CA seeks a Multi-Site Quality Manager to lead the quality program across facilities. You will implement an integrated QMS, drive customer and supplier audits, and improve product and process quality for medical devices.

ITAR compliance and cross-functional collaboration are essential components of this role. The position requires guiding quality strategies, leading investigations, and maintaining data-driven KPI reporting to senior management.