Quality Engineer

Heaviside Industries, Inc.

California (MO)

On-site

USD 90,000 - 130,000

Full time

6 days ago
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Job summary

Heaviside Industries, based in Los Angeles, CA, seeks a Quality Systems professional to lead nonconformance, corrective actions, audits, and FAI activities. You will manage ISO 9001 compliance, document control, risk management, and RMA reporting, ensuring the QMS stays audit-ready across multi-site operations and ITAR considerations.

This role emphasizes formal process discipline, data-driven reporting, exposure to chemical management, and collaboration with manufacturing teams to uphold

Qualifications

  • 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)

Responsibilities

  • Manage the NC(Non-Conformity)-Process (Root Cause – Corrective Action).
  • Drive root cause analysis and corrective/preventive actions.
  • Track and report on nonconformance trends.
  • Plan and conduct internal audits; support future external audits.
  • Ensure compliance with ISO 9001 standards.
  • Support certification and surveillance audits.
  • Plan and execute First Article Inspections (FAI).
  • Review and approve FAI documentation and reports.
  • Identify, assess, and mitigate quality-related risks.
  • Maintain risk registers and support risk review processes.
  • Develop, maintain, and control QMS documents.
  • Manage document control processes (versioning, approvals, distribution).
  • Ensure the QMS is audit-ready.
  • Produce quality reporting for management and stakeholders.
  • Manage RMA reporting and analysis.
  • Track quality metrics and KPIs.
  • Oversee chemical management processes and compliance requirements.

Skills

Nonconformance
Corrective Action
ISO 9001
Audits
FAI
Risk Management
QMS Administration
RMA Reporting
Chemical Management
Documentation

Job description

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.

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