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Quality systems manager • oceanside ca
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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.
Prepare master batch record job folders for new production builds
Archive, physical retains, printed records, and electronic records with scanning, filing, and sorting per quality standards.
Collaborate and support the identify and document defects, nonconformances, or deviations from quality standards.
Stay updated on industry trends, quality standards, and regulations as needed.
Assist with front office incoming receiving and outgoing shipments for both products and supplies.
Effectively communicate quality related information to supervisors, colleagues, and other relevant stakeholders.
Comply with ISO 13485 Quality Management System, FDA 21 CFR Part 820 Quality System Requirements (QSR), and medical device industry requirements.
Competency :
Education and Experience :
Benefits Include :