axon
Manufacturing Quality Engineer II
At a Glance
- Location
- Phoenix, Arizona, United States
- Experience
- 3+ years
- Posted
- 2026-03-04T10:34:25-05:00
Key Requirements
Required Skills
Certifications
- ISO
- Six Sigma
Domain Knowledge
- Engineering
- Manufacturing
Benefits & Perks
ll Medical, Dental, Vision insurance Fitness programs and wellness support L
Requirements
3+ years of experience in a production/manufacturing quality engineering role.
Experience with CAPA, RCA/8D, PPAP, FAIR, PFMEA, and validation activities.
Strong knowledge of IPC-A-610 and relevant industry standards.
Strong understanding of engineering drawings, specifications, GD&T, and inspection techniques.
Experience with Quality Management Systems (QMS), ISO 9001 or AS9100 is a plus.
Internal or external audit experience preferred.
Compensation & Benefits
Competitive salary and 401(k) with employer match
Discretionary paid time off
Paid parental leave for all
Medical, Dental, Vision insurance
Fitness programs and wellness support
Learning & development opportunities
Responsibilities
As a Manufacturing Quality Engineer II, you will be a key member of the Global Quality team.
You will support the full product lifecycle, ensuring high-quality manufacturing processes and products that meet or exceed Axon’s standards and customer expectations.
Participate in the Axon Product Lifecycle (APL) process to ensure compliance with quality deliverables including issue resolution (CAPA), validation plans, CTQ identification, FAIR/PPAP documentation, and quality monitoring implementation.
Lead nonconforming material review (NCMR/MRB) and manage material dispositions with cross-functional teams.
Drive and manage 8D investigations and root cause analysis (RCA); implement effective corrective and preventive actions.
Develop and maintain FAIRs, PPAP documentation, and AQL sampling plans for incoming, in-process, and final inspections.