What are the responsibilities and job description for the Quality Assurance Associate position at SpiTrex - 3D?
Salary: $25 - $30/hrReady 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 buildsSupport 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 neededQuality 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.CommunicationEffectively communicate quality related information to supervisors, colleagues, and other relevant stakeholders.ComplianceComply 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 InsuranceShort Term Disability401(k) plus matchVacation daysPaid holidays
Salary : $24 - $31