Manager, Quality Salary at Kamet BETA

Neptune Medical is a venture backed medical device company based in Silicon Valley. We design, manufacture, and commercialize medical devices based on our proprietary Dynamic Rigidization™ technology. Pathfinder® is our first FDA-cleared commercial device incorporating this novel technology. This advanced endoscopy device is being used at a growing list of leading U.S. hospitals and academic medical centers. Now, the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Triton Robotic Endoscopy will disrupt flexible endoscopy and set a new standard in outcomes for decades to come. TITLE: Manager, Quality Assurance & Regulatory Compliance POSITION SUMMARY: We are seeking an experienced and skilled Manager of Quality Assurance and Regulatory Compliance to lead our organization's quality assurance and compliance efforts. This role involves developing, implementing, and maintaining quality systems and compl

Responsibilities: Oversee QA operations, including inspections, supplier management, root cause analysis, and product reliability. Develop and maintain quality management systems, including training programs. Lead internal audits and external certifications for compliance with industry standards. Drive quality improvement initiatives and manage customer complaints with preventive measures. Engage clients through regular quality meetings and action plans. Lead and develop the QA team, fostering accountability and continuous improvement. Qualifications: Experience: 5+ years in QA, including 3+ years in management. Education: Bachelor's degree in Engineering, Math, or related fields. Skills: Strong analytical and problem-solving abilities. Fluent in Chinese and English with excellent communication skills. Familiar with SMT processes, IPC-610/600 standards, SPC, Lean Manufacturing, and Six Sigma. Preferred: Experience with IATF 16949, ISO 26262, or ISO 13485. Other Requirements: Strong str

USI / Asteelflash is actively looking for a talented another Quality Management Systems Engineer to join our team here in Milpitas, CA. This ideal candidate will be responsible for maintenance and continuous improvement of Asteelflash quality systems. meet the ISO requirements for conformance to procedures, and continuous improvement. RESPONSIBILITIES: Develop audit plans and schedules. conduct internal/external audits. Act as an ISO lead auditor. Communicate non-conformances with the result of internal/external audits and oversee the effectiveness of Corrective and Preventive Action plans. Strong professional interpersonal and communication skills, both verbal and written. Ensure Asteelflash procedures are properly documented, managed, and practiced. Ensure controls and measurements specified in our QMS are in place and drive process and quality good documentation practice improvements. Meet deadlines and multi-task efficiently. Comfortable in a fast-paced environment changing priorit

Reality Labs is seeking an experienced medical devices quality management professional to own the establishment and ongoing operations of a quality management system (QMS) compliant with 21 CFR, EU MDR, and ISO 13485 for the organization. This role will work cross functionally in an organization that is primarily consumer electronics focused but has a growing medical device portfolio to champion the adoption of processes. You will act as the directly responsible individual for the QMS, be an internal consultant to other functions adopting new standard operating procedures, and share their domain experience in electromechanical devices and/or in software as a medical device (SaMD) in product core teams. Medical Devices, Quality Management Systems Engineer Responsibilities Leverage operational experience to meet quality and regulatory goals, define quality management system processes for a medical device product area residing within a larger consumer electronics division. Establish proce

Triple Ring Technologies, Inc. offers a unique environment for talented individuals interested in undertaking varied technical challenges, primarily in medical device and life science industries. Headquartered in Newark, CA, we are an innovative research and development company that partners with clients to deliver complex technical solutions. Our highly interdisciplinary team includes senior professionals from industry, finance, and academia, with extensive experience in medical device, life science, clean tech, security, and industrial technologies. We rely upon each other for technical excellence, real-world engineering and commercial wisdom. Learn more at www.tripleringtech.com. Job Summary The Manager of Quality Assurance will maintain and lead the implementation of Triple Ring's Quality Management System (QMS) for client projects. He/she will work collaboratively with project leadership and other team members to develop, coordinate, and own the QMS elements of a project. These wi

Sustaining Product Quality Manager Cupertino,California,United States Operations and Supply Chain Imagine what you could do here. At Apple, new insights 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 create 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** Are you passionate about Quality Engineering, data analysis, and solving some of the world's most sophisticated problems? Join the dynamic Sustaining Product Quality Engineering team! We partner closely with Engineering, Operations, and AppleCare teams to ensure our custome

Required Skills B.S. in Electrical Engineering or an equivalent technical discipline. 10+ years of experience in customer quality engineering involving integrated circuits. Expert in 8D problem resolution process. Direct customer facing experience in quality manager role. Must have problem solving skills on semiconductor products and manufacturing processes. Must have excellent technical writing in organized and concise manner based on facts and data. Must be available to travel to customer sites worldwide will be as required.

About Glyphic: At Glyphic Biotechnologies, we plan to create the protein revolution for which scientists and researchers have been waiting. We are developing a massively parallel, single-molecule proteome sequencing platform that will transform life science discovery and usher in a new era of insights into human biology and disease. To date, we have raised >$50M from venture partners and non-dilutive grant funding to achieve our vision of next generation proteome sequencing. What we are looking for in you: Glyphic is seeking an experienced quality and analytical development leader who will report to the Chief Operating Officer and anchor a newly formed Quality Control & Analytical Development team focused on establishing an internal core facility to centralize Glyphic's current analytical development activities while building out a phase appropriate Quality Control program in support of a commercial launch. This will be a unique opportunity to design and implement new analytical proces