Manager, Quality Engineering Salary at Bluepoint Controls Inc BETA

About Aivres Aivres is a leading global data center and cloud computing solutions provider committed to delivering innovative technologies that propel the world’s leading industries to new frontiers. We deliver and deploy robust, performance-optimized, purpose-built platforms to major data centers around the globe. Primary Responsibilities Manage the quality of L6-L11 manufacturing process, including but not limited to IQC, PQC, OQC, customer complaint handling, outsourcing on-site management, etc.; Led local QC & QE quality assurance work to ensure the quality of outgoing products to reach the standard; Build, optimize, upgrade and localize the quality system to ensure the quality assurance system meets the company and customer requirements; Cooperate with manufacturing, engineering, R&D and other departments to continuously improve product quality and customer satisfaction; Hold local quality activities such as product quality planning, training, product quality improvement activitie

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

The Senior Customer Quality Manager will be the champion of quality in promoting customers’ perception of our client's products. You must have a proven track record of having worked in a similar role in a semiconductor company. Specific responsibilities include, but are not limited to, the following. Lead, coach and manage quality engineering team. Directly interface with customers on quality maters Collaborate with functional teams (Failure Analysis Engineering, Test Engineering, Product Engineering, Field Sales Organization) to achieve quality goals and customer satisfaction. Requirements: 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. Preference given to candidates with verbal and written t

TITLE: SR. THIN FILM MANUFACTURING ENGINEER FLSA STATUS: EXEMPT REPORTS TO: DIRECTOR, THIN FILM MANUFACTURING ENGINEERING SUMMARY: Under the direction of the Director of Thin Film Manufacturing Engineering , the Sr. Thin Film Manufacturing Engineer is responsible for the monitoring, sustaining, and supporting day-to-day thin film manufacturing processes utilizing ion beam techniques, including providing technical support to ensure process reliability; verifying process robustness with characterization of process latitudes through experimentation; improving the efficiency of deposition and/or dry etching processes; developing and implementing practices or methodologies which reduce cost and improve operational efficiency; conducting root cause analysis and implementing corrective action; and improving production yields via process/tool manufacturability optimization. This position is located in Milpitas, California. ESSENTIAL FUNCTIONS: Monitors, sustains, and supports day-to-day thin f

Description: The candidate will be the champion of quality in promoting customers’ perception of company products. The candidate will ensure customer satisfaction by managing quality standards and customer expectations. The candidate will work seamlessly with various functional groups within the company and its supply base to secure customers’ approval of PI products, facilitate customer audits, ensure timely resolution of product quality problems, and drive corrective and preventive actions as needed. The candidate will act as the technical interface on quality matters with customers. As such, the candidate must have quality systems expertise with excellent organizational and communication skills. The candidate must have a proven track record of having worked in a similar role at a semiconductor company. Specific responsibilities include, but are not limited to, the following. Lead, coach and manage quality engineering team. Directly interface with customers on quality maters Collabor

MAJOR DUTIES AND RESPONSIBILITIES Responsibilities will include, but not be limited to: Senior technical resource for processes, systems, and equipment for Manufacturing Engineering at Elixir. Requires detailed technical knowledge of processes and systems. Must be able to develop new processes, optimize existing processes and systems, and design for future requirements Develop Manufacturing Engineering projects to improve quality, capacity, and cost. Lead cross-functional stakeholder groups for projects. Analyze benefits vs investment for initiatives. Manage projects and resources from initiation to implementation on-time and on-budget Apply internal and external resources to appropriately address Manufacturing Engineering requirements Mentor junior engineers and technicians in the organization Resolve manufacturing equipment issues Work with the R&D team to develop and optimize manufacturing processes Maintain compliance with FDA and ISO guidelines for medical device development and m

MAJOR DUTIES AND RESPONSIBILITIES Responsibilities include: Support new product development projects to include the following: (1) Design control, risk management, biocompatibility, verification/validation testing, sterilization, packaging, and change control. Provide Quality Engineering leadership and support for commercial medical device production: (1) Test method assessment and improvement (Test Method Validation, GR&R). Perform data analysis, trending, change control, and deviation support activities. (2) NCR, Complaints and CAPA investigation and review, including: risk analysis, impact assessment, root cause analysis tools, and material dispositions. Receiving and Incoming Inspection Process Management: (1) Materials handling and transfer management and improvements. This will include development, clinical, and commercial phase-appropriate controls. (2) Component specification implementation, revision, and management. (3) Provide technical support for routine incoming inspection

Ultimate Staffing is seeking a Production Planner for our client in Milpitas. This is a 100% onsite, Direct Hire role with a starting salary of $90K-$95K based on experience. CANDIDATES MUST COME FROM EMS/CONTRACT MANUFACTURING TO BE CONSIDERED Position Summary: The Planner reports to the Master Scheduler and is responsible for production scheduling, validating documents and tooling for production readiness, deviation processing, work order processing, statusing material for clear to build schedule which includes the function of expediting open purchase orders, and running MRP. The Planner may perform a variety of tasks in accordance with their training, experience, and skill. Essential Functions and Responsibilities: · Processing customer purchase orders · Order backlog maintenance · Delivery note confirmation · Manage all existing as well as develop, propose, and implement new Planning processes, systems, and procedures as deemed necessary. · Attend customer focus team meetings to pl