Quality Engineer Salary at Xoom Corp BETA

Job Description Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. Sanmina Corporation has facilities strategically located in key regions throughout the world. The Sanmina Fremont facility is a full-service enclosure systems solution manufacturing plant. Located in California’s Silicon Valley, this facility produces low-to-mid volume New Product Introduction (NPI) runs to full-scale volume. The Fremont facility offers everything from small piece parts to fully integrated and tested

Title: Quality Engineer Location: Milpitas, CA ISO 13485, Supplier Quality, NC/CAPA, Purchasing Control, 21 CFR 820, Part or Component Qualification, Equipment Verification & Validation activities Essential Skills: Knowledge of Supplier Quality Related activities Exposure to ISO 13485 / 21 CFR 820 / Purchasing Control Equipment Verification/ Validation Part/Component Qualification Supplier Audit Desirable Skills: Proven experience required (including 4+ years of medical devices domain & Supplier management experience preferred). Experience with relevant Supplier Quality requirements is required. Management of complete supplier Quality lifecycle Supplier Audit Part / Component Qualification Verification of Verification & Validation activities (hands on experience on IQ/OQ/PQ activities required) Review & approval of supplier Documentations Supplier Site visits as and when required Supplier NC/CAPA lifecycle Management Weekly/Monthly Project progress dashboard generations Supplier relate

Tempur Sealy is committed to improving the sleep of more people, every night, all around the world. As a leading designer, manufacturer, distributor, and retailer of bedding products worldwide, we know how crucial a good night of sleep is to overall health and wellness. Utilizing over a century of knowledge and industry-leading innovation, we deliver award-winning products that provide breakthrough sleep solutions to consumers in over 100 countries. Our highly recognized brands include Tempur-Pedic®, Sealy® and Stearns & Foster®. We hire people who have a passion for helping others find their best night's sleep. No matter what stage of your career, you can build your future at Tempur Sealy! OUR COMPANY OFFERS GREAT BENEFITS, INCLUDING: Generous Paid Time Off Competitive Medical, Dental & other wellness programs Disability and Life Company Paid Retirement Plan Options Generous Employee Purchase Discounts Pay Range: $63,800 - $90,200 The Tempur Sealy manufacturing site in Richmond, CA is

Neptune Medical is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team Triton robotics at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Our Triton robot will disrupt flexible endoscopy. Triton Robotic Endoscopy will set a new standard in outcomes for decades to come. TITLE: Senior Quality Engineer POSITION SUMMARY: We are seeking an experienced and detail-oriented Senior Quality Engineer to join our dynamic team in the medical device industry. The Senior Quality Engineer will support all phases of the product lifecycle as products transition from New Product Introduction (NPI) to commercial operations. This role requires a strong understanding of manufacturing processes, regulatory standards, and quality management systems, with a focus on sustaining and improving the quality

We are seeking a Senior Quality Engineer to become an integral part of our team. This role is key to ensuring the highest standards of product quality and customer satisfaction. As the primary quality advocate, you will interface with customers, manage compliance activities, and drive continuous improvement initiatives. Key Responsibilities: Act as the primary liaison for customers on quality matters, including product assessments, technical issues, returns, and corrective actions. Represent the company in customer surveys, audits, and site visits. Ensure compliance with performance specifications, documentation standards, and customer expectations, including reviewing and approving design documentation. Coordinate and validate adherence to DCMA requirements for product delivery and support DCMA audits. Organize Customer and Government Source Inspections (CSI/GSI) as required. Perform First Article Inspections (FAI) in line with customer contracts and source control drawings, documenti

Position Summary Reporting to the Senior Manager or Director of Quality, the Quality Engineer will have responsibility of ensuring that processes and products consistently meet established quality standards. While ensuring compliance to internal quality system and applicable regulations, the quality engineer will monitor and improve the quality of operational processes and outputs. His/her/their range of responsibilities will entail designing quality standards, inspecting materials, equipment, processes, and products, developing quality control systems, and determining corrective actions. Qualifications Bachelor's degree in engineering, biomedical engineering or related scientific discipline. 3-5 years’ experience working in manufacturing of finished medical device or related industry. Working knowledge of the FDA Quality System Regulation, ISO 13485, ISO 14971, and the EUMedical Device Directive. Lead auditor credentials for QSR, ISO, or MDSAP are desired (ASQ Certification preferred)

Quality Engineer – Program Support Overview: As a Quality Engineer, you will oversee all quality aspects of assigned programs, ensuring internal performance objectives are met, serving as the primary customer interface, and supporting supplier quality initiatives. Key Responsibilities: Manage program milestones and track key objectives. Conduct preliminary reviews of non-conforming material and evaluate in-process rejections. Oversee drawing control, CCB reviews, and customer notifications for document changes. Perform final test data package reviews before shipment to verify compliance with specifications. Drive supplier quality issue resolution in collaboration with QC, Purchasing, and Engineering teams. Interface with internal teams, customers, and suppliers to address quality concerns and ensure ISO/AS9100 compliance. Lead corrective and preventive action initiatives with interdisciplinary teams. Analyze manufacturing performance, identify trends, and recommend quality improvements

DTEX Systems helps hundreds of organizations worldwide better understand their workforce, protect their data, and make human-centric operational investments. At DTEX, our philosophy towards our business is the same as our philosophy towards technology: people come first. Our future depends on bright, energetic, talented people who share a passion for building the next generation of user behavior intelligence. We invite you to bring your talent to DTEX and help create our future, expanding our reach and influence worldwide. Learn more about DTEX Systems’ mission to proactively protect global organizations from insider threats at www.dtexsystems.com; LinkedIn DTEX Systems: Overview | LinkedIn Why you should choose DTEX as your next career: • Opportunity to be part of a disruptive high growth success story. • DTEX is a great place to work because of its mission-oriented culture and passion for protecting customers. • We offer exciting growth opportunities and an excellent platform for ind