JOB DETAILS
Quality Engineer
CompanyHeaviside Industries
LocationMarina Del Rey
Work ModeOn Site
PostedSeptember 16, 2026

About The Company
No description available for this Company.
About the Role
ABOUT HEAVISIDE INDUSTRIES
Heaviside Industries builds multi-domain autonomous precision munitions for U.S. and allied special operations and conventional forces. While modern warfare has rapidly evolved with the proliferation of unmanned systems, hyper-precise munitions in contested environments are the future of the battlefield. Economical precision strike capabilities are critical to U.S. and allied war efforts, enabling successful defeat of enemy military assets and infrastructure. Heaviside builds precision munitions designed to operate in GPS-denied and spectrum-jammed battlefields—where traditional systems degrade or fail—without inflated prices or sacrifice to performance.
All engineering and manufacturing is conducted in-house in Heaviside’s Los Angeles, CA headquarters and Oslo, Norway office.
Heaviside is backed by Interlagos, Menlo Ventures, Flume Ventures, Cantos, Anorak Ventures, and Ravelin Ventures.
WHAT YOU WILL DO
Nonconformance & Corrective Action
• Manage the NC(Non-Conformity)-Process (Root Cause – Corrective Action)
• Drive root cause analysis and corrective/preventive actions
• Track and report on nonconformance trends
Audit & Compliance
• Plan and conduct primarily internal audits. External will probably be applicable in the future.
• Ensure compliance with ISO 9001 standard.
• Support certification and surveillance audits
First Article Inspection (FAI)
• Plan and execute First Article Inspections
• Review and approve FAI documentation and reports
Risk Management
• Identify, assess, and mitigate quality-related risks
• Maintain risk registers and support risk review processes
Documentation & QMS
• Develop, maintain, and control QMS documents
• Manage document control processes (versioning, approvals, distribution)
• Ensure the Quality Management System is kept current and audit-ready
Reporting
• Produce quality reporting for management and stakeholders
• Manage RMA (Return Merchandise Authorization) reporting and analysis
• Track quality metrics and KPIs
• Chemical Management
• Oversee chemical management processes and compliance requirements
WHAT WE ARE LOOKING FOR
• Strong understanding of nonconformance and corrective action (RC-CA) processes
• Working knowledge of ISO 9001
• Experience conducting or supporting internal/external audits
• Experience with First Article Inspection (FAI) procedures
• Risk assessment and risk management skills
• Document management / QMS administration experience
• Analytical skills for quality and RMA reporting
• Familiarity with chemical management requirements and regulations
• Strong attention to detail and process discipline
• Good written and verbal communication skills for reporting and documentation
• U.S. Person as defined by ITAR (22 CFR §120.62)
NICE TO HAVE
• Experience in a manufacturing or defense industry environment
• Familiarity with ERP/MES systems
• Experience working across multi-site quality operations
• Knowledge about AS9100 and AQAP 2110 standards
ADDITIONAL INFORMATION
Compensation bands are determined by role, level, location, and alignment with market data. Individual level and base pay is determined on a case-by-case basis and may vary based on job-related skills, education, experience, technical capabilities and internal equity. In addition to base salary, for full-time hires, you may also be eligible for long-term incentives, in the form of stock options, and access to medical, vision & dental coverage as well as access to a 401(k) retirement plan.
To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR here. (https://www.pmddtc.state.gov/?id=ddtc_kb_article_page&sys_id=24d528fddbfc930044f9ff621f961987)
Heaviside is an Equal Opportunity Employer; employment with Heaviside is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, physical disability or any other legally protected status.
Heaviside Industries builds multi-domain autonomous precision munitions for U.S. and allied special operations and conventional forces. While modern warfare has rapidly evolved with the proliferation of unmanned systems, hyper-precise munitions in contested environments are the future of the battlefield. Economical precision strike capabilities are critical to U.S. and allied war efforts, enabling successful defeat of enemy military assets and infrastructure. Heaviside builds precision munitions designed to operate in GPS-denied and spectrum-jammed battlefields—where traditional systems degrade or fail—without inflated prices or sacrifice to performance.
All engineering and manufacturing is conducted in-house in Heaviside’s Los Angeles, CA headquarters and Oslo, Norway office.
Heaviside is backed by Interlagos, Menlo Ventures, Flume Ventures, Cantos, Anorak Ventures, and Ravelin Ventures.
WHAT YOU WILL DO
Nonconformance & Corrective Action
• Manage the NC(Non-Conformity)-Process (Root Cause – Corrective Action)
• Drive root cause analysis and corrective/preventive actions
• Track and report on nonconformance trends
Audit & Compliance
• Plan and conduct primarily internal audits. External will probably be applicable in the future.
• Ensure compliance with ISO 9001 standard.
• Support certification and surveillance audits
First Article Inspection (FAI)
• Plan and execute First Article Inspections
• Review and approve FAI documentation and reports
Risk Management
• Identify, assess, and mitigate quality-related risks
• Maintain risk registers and support risk review processes
Documentation & QMS
• Develop, maintain, and control QMS documents
• Manage document control processes (versioning, approvals, distribution)
• Ensure the Quality Management System is kept current and audit-ready
Reporting
• Produce quality reporting for management and stakeholders
• Manage RMA (Return Merchandise Authorization) reporting and analysis
• Track quality metrics and KPIs
• Chemical Management
• Oversee chemical management processes and compliance requirements
WHAT WE ARE LOOKING FOR
• Strong understanding of nonconformance and corrective action (RC-CA) processes
• Working knowledge of ISO 9001
• Experience conducting or supporting internal/external audits
• Experience with First Article Inspection (FAI) procedures
• Risk assessment and risk management skills
• Document management / QMS administration experience
• Analytical skills for quality and RMA reporting
• Familiarity with chemical management requirements and regulations
• Strong attention to detail and process discipline
• Good written and verbal communication skills for reporting and documentation
• U.S. Person as defined by ITAR (22 CFR §120.62)
NICE TO HAVE
• Experience in a manufacturing or defense industry environment
• Familiarity with ERP/MES systems
• Experience working across multi-site quality operations
• Knowledge about AS9100 and AQAP 2110 standards
ADDITIONAL INFORMATION
Compensation bands are determined by role, level, location, and alignment with market data. Individual level and base pay is determined on a case-by-case basis and may vary based on job-related skills, education, experience, technical capabilities and internal equity. In addition to base salary, for full-time hires, you may also be eligible for long-term incentives, in the form of stock options, and access to medical, vision & dental coverage as well as access to a 401(k) retirement plan.
To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Learn more about the ITAR here. (https://www.pmddtc.state.gov/?id=ddtc_kb_article_page&sys_id=24d528fddbfc930044f9ff621f961987)
Heaviside is an Equal Opportunity Employer; employment with Heaviside is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, physical disability or any other legally protected status.
Key Skills
ISO 9001Root Cause AnalysisCorrective and Preventive Action (CAPA)First Article Inspection (FAI)Internal AuditingRisk ManagementQuality Management System (QMS)Document Control
Categories
EngineeringOperations
Benefits
Medical insuranceVision insuranceDental insurance401(k) retirement planStock options
Job Information
📋Core Responsibilities
Own the nonconformance and corrective action process, conduct internal audits for ISO 9001 compliance, plan and execute First Article Inspections, maintain the QMS and document control system, manage quality risk registers, and produce quality and RMA reporting and metrics.
📋Job Type
full time
💰Salary Range
$125,000 - $150,000
📊Experience Level
2-5
💼Company Size
Not specified
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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