MillenniumSoft Inc - United States, Quality Control

Join our team in Irvine as an Entry-Level Quality Engineer. You will support validation, testing, and quality documentation, ensuring compliance with FDA, ISO, and cGMP standards. This role involves cross-functional collaboration, statistical analysis, and protocol execution to maintain product q...

Join our San Jose team as a Quality Assurance Technician I. You will review and process medical device customer complaints, ensuring documentation compliance. This role requires a college degree and 1+ years of relevant experience. Strong analytical and multitasking skills are essential in this i...

Lead a critical compliance project for medical device installation processes in this San Diego-based contract role. Leverage your 10+ years of FDA-regulated quality engineering experience to enhance procedures and ensure regulatory standards. Utilize tools like Root Cause Analysis and drive cross...

Join our team in Salt Lake City as a Data Verification Specialist. You will ensure data accuracy and integrity by examining information, identifying errors, and verifying completeness. This role requires strong attention to detail, proficiency in MS Office, and collaboration with cross-functional...

Join our team as a Complaint Management Specialist in a blended remote/onsite role based in San Antonio. This temporary position requires proven customer service and complaint handling skills, with medical device experience as a major advantage. You will manage the end-to-end complaint process, e...

Join our team in El Paso as a Quality Control Technician. You will implement quality programs, ensure compliance with GLP/GCP/cGMP standards, and support operations. The role requires 1-2 years of experience with measuring tools, reading drawings, and a strong attention to detail. A high school d...

Join our San Diego team as a Quality Control Specialist. Perform routine ELISA/CBA testing, analyze data, and maintain precise documentation in a dynamic lab environment. The ideal candidate has 2+ years of lab experience, strong analytical skills, and a relevant scientific degree. This role offe...

Seeking a Quality Engineer to ensure cGMP compliance and manage supplier quality for medical instrument manufacturing. Requires 3+ years of FDA/ISO-regulated experience and expertise in QSR, GMP, and process troubleshooting. You will oversee investigations, supplier audits, and drive continuous i...

Join our San Diego lab as a Product Test Laboratory Technician. You will perform visual, mechanical, and functional testing on medical instruments and disposables. The role requires meticulous documentation, adherence to GMP/GLP standards, and collaboration with Engineering teams. Ideal candidate...

Join our team in Tempe as a Quality Document Control Specialist. You will manage change requests, create controlled documents, and support a MasterControl system migration. The role requires experience in Medical Device QMS, strong attention to detail, and excellent English skills. Be a key playe...

Join our team in Mannford, OK as a Quality Engineer. You will ensure product quality and compliance with FDA/ISO standards in the medical device/pharma sector. Key duties include validation, statistical analysis, and cross-functional collaboration. A BS degree and 2+ years of GMP experience are r...

Join our San Diego biotech team as a Quality Control Specialist. You will perform routine QC testing, including essential flow cytometry, following strict protocols. The role requires a scientific degree, 2+ years of lab experience, and strong analytical skills. You'll ensure accurate data report...