Quality Engineer Salary at Aheadtek BETA

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

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

As a Quality Engineer ,you will play a critical role in supporting the technical needs of our customers. You will be responsible for building strong relationships with key stakeholders, understanding their engineering and quality requirements, and delivering tailored support and solutions that drive their success. Your technical acumen, interpersonal skills, and exceptional writing abilities will be essential in conveying our value proposition and securing new business opportunities. Responsibilities Use statistical analysis approaches to analyze and improve quality KPIs. Periodically report and present performance metrics to key stakeholders. Collaborate with a cross-functional team to identify root causes, take corrective actions, and propose preventive actions in an event of excursions or quality incident. Collaborate with suppliers to ensure the quality of incoming materials used in the manufacturing line. Support internal auditing activities that would drive continuous improvement

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

Senior Quality Engineer – Class III Medical Device Location: San Francisco Bay Area Requirements: 5 days a week onsite No Sponsorship options A leading Class III medical device company in the Bay Area is seeking a Senior Quality Engineer to drive quality assurance initiatives and ensure compliance with FDA, ISO 13485, and other regulatory standards. This role will focus on design control, risk management, CAPA, and process validation to support the development and manufacturing of life-saving medical technologies. Key Responsibilities: Lead quality engineering activities in product development, design control, and risk management. Develop and execute process validations (IQ/OQ/PQ) and statistical data analysis. Support CAPA investigations, root cause analysis, and continuous improvement efforts. Ensure compliance with FDA 21 CFR 820, ISO 13485, and ISO 14971. Collaborate cross-functionally with R&D, manufacturing, and regulatory teams. Qualifications: Bachelor’s degree in Engineering o

FranklinWH is a rapidly expanding company determined to become the leader in the global energy home storage system (ESS) industry. FranklinWH offers whole home energy solutions typically coupled with solar PV systems, bringing households into the modern all-electric future. Though founded by experts in power electronics, BMS and EMS, FranklinWH is equally focused on energy management software while also providing top level service to our partners and customers. FranklinWH is expanding its global footprint, relying on an industry leading supply chain. This is an exciting time to be at a fast-growing company in a fast-accelerating industry. Job Responsibilities: Supervise and manage suppliers' process quality, including daily, weekly, and monthly quality meetings. Continuously identify process quality risks through PFMEA and improve the process quality control plan. Conduct quality assessments for NPI (New Product Introduction) and establish quality standards. Perform production line aud

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)

Manufacturing Quality Engineer Cupertino,California,United States Operations and Supply Chain Imagine what you could do here. At Apple, new ideas have a way of becoming extraordinary products, services, and customer experiences very quickly. Bring passion and dedication to your job and there's no telling what you could accomplish. The people here at Apple dont just build products they craft the kind of wonder thats revolutionized entire industries. Its the diversity of those people and their ideas that encourages the innovation that runs through everything we do, from amazing technology to industry-leading environmental efforts. Join Apple and help us leave the world better than we found it. **Description** In this highly visible role, you will have the opportunity to make a significant impact on Apple Products and leave a footprint for years to come. We have an opportunity for an accomplished quality engineer to lead development, and ramp for a next generation Apple product. Our quali