Quality Assurance Associate
Company: SpiTrex - 3D
Location: Carlsbad
Posted on: February 24, 2026
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Job Description:
Job Description Job Description Salary: $25 - $30/hr Ready to
Transform Your Career? Join SpiTrex 3D! Are you looking to be part
of a dynamic team in the cutting-edge world of additive
manufacturing? Do you thrive in a fast-paced, growing environment
that blends high technology and USA manufacturing? If so, we have
the perfect opportunity for you! We are a leading additive
manufacturing company located in vibrant Carlsbad, California. Our
innovative solutions are revolutionizing the industry, and we're
seeking a talented Quality Assurance Associate to join our growing
team. Imagine a workplace where your growth knows no bounds - where
data drives success, and your career flourishes. We believe SpiTrex
3D is a workplace like no other. It is a place to be challenged,
explore your curiosity, and grow your career. Job Overview: As a
Quality Assurance Associate at SpiTrex 3D, you will play a crucial
role in ensuring the highest standards of quality for our 3D
printed products and services. Your focus will be on supporting and
organizing critical Master Batch Records (MBRs) and Certificates of
Conformances while supporting quality control activities such as
with data entries (ERP System), lean manufacturing/scheduling,
record archiving, documenting training records, and supporting
change controls. Essential Functions: Company Culture and Mission:
Consistently apply core values (Integrity, Impact, Dedication) to
your decision-making process and interactions with others. Uphold
and contribute to the companys quality policy commitment. Master
Batch Records: Prepare master batch record job folders for new
production builds Support and organize records and data entries to
allow for approvals in a timely manner with an accurate compilation
of product Master Batch Records, which include Certificates of
Conformance. Assist in verifying manufacturing scheduling to ensure
that all quality activities are occurring at or ahead of schedule.
Using Microsoft Word, Excel, and JobBoss2 document and record data
entries in cooperation with handwritten records. Review executed
records for compliance, ensuring completeness of all necessary
testing and documents across various processes as needed Quality
Control Records: Archive, physical retains, printed records, and
electronic records with scanning, filing, and sorting per quality
standards. Ensure product processes adhere to established quality
standards and guidelines. Support data collection and monitor data
throughout the production process where needed. Defect
Detection/nonconformances: Collaborate and support the identify and
document defects, nonconformances, or deviations from quality
standards. Work closely with quality leadership and production
teams to address and resolve quality issues promptly. Support
corrective actions to prevent recurrence of defects as needed.
Training and Education: Stay updated on industry trends, quality
standards, and regulations as needed. Support the maintenance of
training records and training matrixes. Shipping Receiving: Assist
with front office incoming receiving and outgoing shipments for
both products and supplies. Assist in developing and performing
quality checks and documentation for incoming materials.
Communication Effectively communicate quality related information
to supervisors, colleagues, and other relevant stakeholders.
Compliance Comply with ISO 13485 Quality Management System, FDA 21
CFR Part 820 Quality System Requirements (QSR), and medical device
industry requirements. Assist in the implementation of the quantity
management system. Other work-related tasks as assigned.
Competency: Understanding of quality control principles and
inspection techniques. Strong understanding of GMPs and GDP for
production and generation of batch records. Basic familiarity with
mechanical testing and materials characterization. Excellent
organizational skills. Basic ability to read and interpret
engineering drawings and specifications. Problem-solving and
troubleshooting skills. Organizational and time management skills.
Very strong attention to detail. Strong commitment to safety and
quality assurance. Effective communication and interpersonal skills
to work with cross-functional teams. Education and Experience:
Associate degree in related field and/or 18 months-4 years
experience preferred. Experience in quality control in the medical
device industry, aerospace, or automotive industry preferred.
Experience with mechanical testing and materials characterization
preferred. Benefits Include: Medical, Vision and Dental Insurance
Short Term Disability 401(k) plus match Vacation days Paid
holidays
Keywords: SpiTrex - 3D, Aliso Viejo , Quality Assurance Associate, Science, Research & Development , Carlsbad, California
