Quality Technician Jobs in San Jose, CA

Ultimate Staffing is seeking Quality Inspectors for our client in San Jose. This is a 100% onsite, temp to perm swing shift positions starting at 1:30pm to 10pm. (Day Shift for the first 2 months) Monday-Friday with opportunity for overtime. Details: Quality Technician These are the skills we're looking for: § Attention to detail § Read engineering drawings § Inspection skills § Communication skills § Documentation skills § Technical skills § Basic Math skills § Basic Computer Skills § Experience with ERP § Organization Skills § Written and verbal communication skills § Able to lift 50lbs § Reporting skills § Hand/eye coordination § High School diploma or equivalent Shift: Swing Pay rate: $29 to $35 If you are interested in the role email resume to All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Sentien Robotics is a cutting-edge technology company, redefining what's possible with unmanned aerial systems (UAS) and robotics. Our mission is to deliver innovative solutions for critical industries like surveillance, environmental monitoring, infrastructure inspection, and national security through persistent aerial flight, multi-UAS coordination, and full lifecycle automation. Role Description As a Production Technician, you'll assemble, troubleshoot, and maintain robotic systems, ensuring they meet our high standards of quality and safety. You'll work closely with engineers and follow detailed assembly instructions, contributing directly to the success of our groundbreaking technology. Responsibilities • Assemble mechanical, electrical, and robotic components. • Manage inventory and prepare components for assembly. • Conduct quality checks throughout the production process. • Diagnose and resolve assembly issues and perform preventive maintenance. • Interpret technical drawings and maintain accurate records. • Support critical hardware demonstrations with customers as needed Qualifications • Experience with hand and power tools in a production setting. • Ability to read mechanical drawings and schematics. • Strong attention to detail and organization skills. • Prior experience in robotics or automation is a plus. • Technical degree or certification preferred. Why Sentien Robotics? Join us in shaping the future of robotics. You'll be part of a fast-paced, innovative team working on impactful real-world projects with opportunities for growth and professional development. US Hourly Range $32-$40 USD

We are seeking a dedicated and detail-oriented Quality Specialist to join our team at a leading Appliances, Electrical, and Electronics Manufacturing company in Concord, CA. In this role, you will play a critical part in ensuring the highest quality standards are maintained throughout the manufacturing process for our products. You will collaborate with various departments to implement and uphold quality control measures, ensuring compliance with industry standards and customer requirements. Key Responsibilities: Conduct regular inspections and audits of manufacturing processes, components, and finished products to ensure compliance with internal and external quality standards. Conduct root cause analysis of quality issues and implement continuous improvement initiatives to prevent recurrence. Develop, implement, and maintain quality control procedures, standards, and specifications for the production of appliances, electrical, and electronic products. Review and analyze data related to product defects, production processes, and customer feedback to identify areas for improvement. Assist in the development and execution of test protocols, inspections, and documentation to ensure quality assurance compliance. Monitor and maintain records of quality metrics, non-conformances, and corrective actions taken. Collaborate with suppliers to ensure the quality of incoming raw materials and components. Work closely with the production and engineering teams to resolve quality issues and implement corrective actions. Ensure that products meet safety, regulatory, and industry-specific standards (e.g., UL, CE, ISO, etc.). Assist in training and educating team members on quality standards and best practices. Maintain up-to-date knowledge of industry trends, quality control techniques, and regulatory requirements. Qualifications: Bachelor's degree in Engineering, Manufacturing, Quality Assurance, or a related field (preferred). Minimum of 3 years of experience in quality control or quality assurance in an appliance, electrical, or electronics manufacturing environment. Strong knowledge of quality management systems, industry standards, and regulatory requirements (e.g., ISO 9001, UL, CE). Experience with inspection tools and techniques such as calipers, micrometers, and other measurement devices. Proficient in data analysis and problem-solving using software tools (e.g., Excel, Minitab, SAP). Detail-oriented with a keen eye for identifying and solving quality-related issues. Ability to thrive in a fast-paced, dynamic work environment and manage multiple priorities. Strong communication and interpersonal skills with the ability to work cross-functionally with various teams. Salary: $70k-75k + Bonus + Benefits If you are interested, don't hesitate to apply!

Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. As a team, we've launched two satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $500 million from top global investors, and recruited a team of over 300 world-class engineers. We all work out of our (legendary) San Francisco office, which was once used to build ships during the World Wars. Our satellites, which operate from geostationary orbit (GEO), weigh only 400 kg and utilize a proprietary software-defined radio payload. Each satellite can connect over two million people, and we're very excited for the impact we'll soon have in the Philippines, Peru, Mexico, and more! Backed by substantial funding and a passionate, collaborative team, we offer a rewarding work environment where you'll learn and make a significant impact, no matter where you are in your career. Apply and join us on our journey towards global connectivity! Production Quality Inspector As a Production Quality Inspector, you are responsible for being the last line of defense in assuring mission success. You will work with the most cutting edge MicroGEO satellite technology and perform inspections in several workcenters to verify our hardware meets the highest level of quality. The ideal candidate is self-driven, extremely detail oriented, and seeks a highly cross functional dynamic environment. Responsibilities Perform in-process inspection and final verification of flight hardware to drawing, process specifications, and work order requirements supporting multiple work centers (assembly, integration, wire harnessing, or test) Identify, document, and verify resolution of production and test non-conformances in accordance with prescribed procedures and pursue corrective action as required Interface with engineering and production to communicate and help resolve nonconforming issues Independently perform verifications and document results in a clear, precise, and complete manner Support quality management system policies and procedure documentation, assess compliance to company and industry standards, initiate and lead continual improvement and lean manufacturing initiatives Perform other related duties, as assigned, for the purpose of ensuring an efficient and effective work environment Requirements 3+ years of inspection experience in an aerospace, military or manufacturing environment Substantial knowledge of the control of nonconforming hardware, failure/root cause analysis, corrective and preventive action processes Experience reading and interpreting design drawings and CAD models Experience with performing electronic testing and inspection using portable measuring devices and lab equipment (microscopes, testers, scopes, etc) Excellent communication (written and verbal) and teamwork skills Ability to work independently with a strong work ethic, be innovative, detail oriented, possess initiative, and team oriented Willing and able to work overtime and/or weekends as required Bonus Associate degree or higher in quality, engineering, or related field Knowledgeable with ISO 9001/AS9100 quality management systems Experience inspecting solder, crimping, conformal coating, staking, and surface mounted devices in accordance with IPC-J-STD-001 or IPC-A-610 standards Wire harness experience in accordance with IPC-A-620 standards Six Sigma Yellow/Green Belt certified What we offer: All our positions offer a compensation package that includes equity and robust benefits. Base pay is a single component of Astranis's total rewards package, which may also include equity in the form of incentive stock options, high quality company-subsidized healthcare, disability and life insurance benefits, flexible PTO, 401(K) retirement, and free on-site catered meals. Astranis pay ranges are informed and defined through professional-grade salary surveys and compensation data sources. The actual base salary offered to a successful candidate will additionally be influenced by a variety of factors including experience, credentials & certifications, educational attainment, skill level requirements, and the level and scope of the position. Base Hourly Pay $30 - $40 USD U.S. Citizenship, Lawful Permanent Residency, or Refugee/Asylee Status Required (To comply with U.S. Government space technology export regulations, applicant must be a U.S. citizen, lawful permanent resident of the United States, or other protected individual as defined by 8 U.S.C. 1324b(a)(3)) Our mission and our products are meant to connect the world and everyone in it, regardless of gender, race, creed, or any other distinction. We believe in a diverse and inclusive workplace, and we encourage all people to join our team and bring their unique perspective to help make us stronger.

Title: Manufacturing Tech - Cell Therapy Duration: 2 year contract Responsible for clinical manufacturing of monoclonal antibodies (mAB) Drug substance within the Cell Culture Technology Center (CCTC). Collaborates closely with biological development (BD) and Manufacturing Science and Technology (MSAT) for new product introductions and ensure platform alignment. POSITION DUTIES & RESPONSIBILITIES • Responsible for all aspects of clinical manufacturing in the following areas: Cell Therapy, Cell Expansion, Cell Culture, Purification, Solution Preparation and Weigh/Dispense. Including freezing and put away products. • Employee will move with the process and work seamlessly across all areas. • Ensures all activities are performed to schedule. • Manufactures products in various phases of product life cycles from clinical thru launch. Clearly understands, communicates, and manages differences in terms of documentation, sample handling, automation and cGMPs etc. for different phases of product life cycle. • Provide feedbacks to handles and troubleshoots single use technology (SUT) from end to end in manufacturing process. • Works cross functionally to ensure process is controlled and issues are escalated and investigated. • Redlines and reviews controlled documents for various equipment/processes. • Effectively employs all methods of communication (oral, written, presentation) to ensure knowledge and information transfer across shifts, to management, and cross functionally. • Raises and supports investigation of deviations. • Participates in safety investigations for CCTC and promotes safe behaviors at all times. REQUIREMENTS - Minimum of BS in science related field is preferred - Transferable skills will be considered. or an equivalent combination of education and experience. Cell Therapy and/ or Stem Cell Experience - Must have minimum of 1+ years' experience. - Must be Experienced in cGMP and GDP requirements for pharmaceutical manufacturing. • Experienced with business IT systems (Delta V, Team, outlooks, SAP etc…) Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Design Quality Engineer Reporting to: Director of Quality JOB SNAPSHOT Base Pay - Negotiable Employment Type - Full-Time Job Type - Engineering Education - 4 Year Degree Experience - Minimum 3 years Manages Others - No Industry - Medical Devices Required Travel - Occasional ABOUT NEUSPERA MEDICAL, INC. Neuspera Medical, Inc. is an exciting early-stage medical device company with a uniquely positioned neuromodulation technology platform, headquartered in San Jose, CA. Neuspera is committed to developing implantable medical device technology that will improve the lives of patients battling chronic illness. With the first intended indication for use as Urinary Urgency Incontinence (UUI), the platform technology is ultimately designed to deliver targeted bioelectronic medicine for a variety of conditions. Neuspera's minimally invasive implants with external wearable transmitters offer the possibility for therapies to reach deeper, harder to access anatomical locations in the body. WHY NEUSPERA? Take the next step in your career and join Neuspera today to change lives through the products we help create. Here, you will contribute your talents to meaningful projects that impact the lives of patients around the world and develop as an individual by working directly with a team of seasoned experts and rising stars. Our values of accountability, respect, tenacity, results, and integrity are embedded in everything we do. No matter what your role may be, Neuspera strives to ensure all our employees are empowered and given the necessary tools to lead us in our relentless pursuit of success. PRIMARY FUNCTION Quality Engineer supporting manufacturing operations and design transfer. Key areas of support include incoming and in-process inspection, MRB, quality systems, process validations and test method validation. This position is expected to take a hands-on approach on all aspects of quality engineering and quality systems. JOB DUTIES Work with Manufacturing, R&D, Regulatory, and Clinical to meet clinical and commercial milestones Provide daily quality support to incoming inspection and manufacturing activities Review and monitor processes for Receiving and In-Process Inspection, Calibration / Preventive Maintenance, Nonconforming Materials, Product Testing, and Finished Goods Release Maintain quality system and participate in internal/external audits to ensure compliance with FDA regulations and ISO 13485 Review investigations of device deficiencies/complaints Review changes in manufacturing processes and support process validation activities (IQ, OQ, PQ) Collaborate with engineers to evaluate and validate applicable test methods Lead MRB activities to investigate nonconformances and identify root cause and corrective actions Initiate changes to improve quality systems and processes Conducts supplier qualification and maintenance activities Evaluate quality performance data and present results to the management team Other responsibilities as assigned JOB REQUIREMENTS Basic understanding of the medical device industry including 21 CFR Part 820 and ISO 13485 Basic understanding of mechanical and/or electrical engineering Experience with sterilization and statistical analysis QUALIFICATIONS AND EXPERIENCE Bachelor's degree in Engineering, Science or similar field Results driven, collaborative team player capable of working well with others, as well as autonomously with little direction Ability to adapt to dynamic situations and adjust as we grow Experience with software validations a plus COMPENSATION Based on market data and other factors, the salary range for this position is $100,000 - $125,000. However, a salary higher or lower than this range may be appropriate for a candidate whose qualifications differ meaningfully from those listed in the job description. WORK ENVIRONMENT Office and laboratory Some travel necessary Foster work culture of; Diversity and inclusion, honesty and integrity, accountability and teamwork, proactive communication focused on results that is based on facts and is respectful

The client is hiring Data Engineers with experience in data quality and model training. The role involves processing data for machine learning models, writing custom scripts, building automation tools, and assessing the effectiveness of data through quality checks. Responsibilities: Data Quality & Processing: Ensuring the data is clean, formatted correctly, and is of high quality for machine learning models. Custom Code: Writing custom code to process data, perform quality checks, and automate processes. Model Training: Using data to train machine learning models, assessing the impact of data on the model's performance. Reporting: Conducting quality analysis and reporting on the data and model performance (e.g., identifying and removing low-quality data). Automation Tools: Building automation to feed data into models and analyze outcomes. Experience: Proficiency in Python (with experience in writing and debugging scripts). Knowledge tools like Jupyter Notebooks to write and run code for data processing. Experience with data quality checks (both manual and automated). Familiarity with using data from public domains like Hugging Face and GitHub. Understanding of machine learning models, particularly in training and assessing model quality. Exposure to basic machine learning concepts, including working with open-source models like Gamma. Skills: Data Quality Coding (Python) Machine Learning Knowledge Model Training Prompt Engineering (Desired) Writing prompts for GenAI Models (Desired) Education: Bachelor's degree in STEM, Computer Science, Data Analysis, or related field. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Deepak Email: ******************************* Internal Id: 24-28066

Sheathing Technologies, Inc., founded in 1992, is a medical device manufacturer of Ultrasound Probe Covers, FDA-Cleared Viral Barriers, Adhesives, Needle Guides Kits, Ultrasound Gel, and Storage/Transport Covers. We are the global leader of infectious control solutions. More than 99% of our products are manufactured in the United States with the bulk of it right in our facility located in Morgan Hill, CA. As market leaders, our technological advancements for ultrasound procedures have enabled us to continually increase quality, year after year. We are looking to expand our team and are now accepting applications for an In-Process Quality Inspector II. Our biggest accomplishment in recent history has been to develop and create the world's only FDA cleared Viral Barrier - providing infectious control and save people's lives. This product provides our clinicians and their patients with a complete barrier to all bacteria and all currently known testable viruses. Sheathing Technologies, Inc. is committed to providing a comprehensive benefits package to all of the company's employees. We offer standard benefits such as medical, dental and optional vision coverage, life insurance, 401(k) matching plan & tuition reimbursement. The benefits offered by Sheathing Technologies, Inc. is designed to positively impact all aspects of your life; to help you and your family succeed and to maintain our status as a “perfect job”. Come find out what Sheathing Technologies, Inc. has to offer you. As an In-Process Quality Inspector II in our Morgan Hill, CA facility your essential duties & responsibilities will be: Inspection Activities Perform accurate physical and visual inspections of raw materials, components and assemblies, and final product as per Inspection plans or specification requirements. Determine whether the product conforms to product specifications. Initiate non-conformance reports as required. Detecting, correcting, and preventing waste or loss of raw material or partially finished product. Perform verification for all the labels by either visual or scanning methods. Review the daily line clearance to verify that all the equipment, tools, and fixtures used on the manufacturing floor are within the calibrated due dates. Verify the revisions of the kitted components are the current revisions, and that the kitted materials are within expiration dates if applicable. Manufacturing History Record Review Activities Perform lot history record review for the sub-assemblies, final assembled devices, and finished goods packaging Review final test records to verify that the test results are complete and pass. Review manufacturing test records to verify that the test results are complete and pass. Provide training and/or guidance to other Quality In-process Inspection personnel. Contributes to the development of quality systems working instructions. Reads and interprets sampling plans to determine sample size and/or accept/reject criteria Release products to the designated location Additional Requirements Assist with data collection for tracking and trending purposes. Complies with documentation and FDA procedures and policies Identify and implement opportunities for continuous improvement - under supervision Strong attention to detail and ability to identify minute defects Proficiency in using measuring tools and testing equipment Knowledge of quality control methodologies and standards Good analytical and problem-solving skills Ability to work independently and as part of a team Excellent documentation and reporting skills Basic understanding of manufacturing processes Associate degree and 1-3 years of experience in quality inspection or manufacturing or High school diploma or GED and 4 - 6 years of experience in quality inspection or manufacturing. Demonstrated ability to develop, communicate, and influence solutions to complex problems. Demonstrated experience with Microsoft Suite packages (Word, Excel) Must be able to complete detailed documentation accurately. Exercises judgment within well-defined and established procedures and practices to determine appropriate actions. Shows strong initiative and independence. Able to perform routine work and fulfill responsibilities with little or no additional instruction. Detail-oriented with good organization and time management skills. Strong interpersonal and verbal/written communication skill required. Ability to effectively participate and contribute on multi-disciplinary teams. Salary: $27.50 - $35 per hour

Senior Quality Engineer - Santa Clara, CA - $150k - $160k No C2C Join an innovative leader in the cardiovascular medical device industry. Founded in 2005, this forward-thinking company specialises in integrated solutions designed to improve patient outcomes in vascular treatments. Their portfolio includes advanced carotid PTA balloon systems with embolic protection, peripheral balloon angioplasty systems, and cutting-edge thrombectomy devices. Position Overview: Could you be the next Senior Quality Engineering professional to join my client's dynamic team? As a Senior Quality Engineer, you will be an integral part of a dynamic team, driving quality initiatives across the entire product lifecycle. With a primary focus on manufacturing and commercialization, your work will directly support the development and delivery of life-saving cardiovascular treatments. Key Responsibilities: Lead quality aspects of complaint investigations, CAPAs, and nonconformance. Partner with Manufacturing Engineering to improve yield, reduce costs, and optimize supply chains, ensuring all performance requirements are met or enhanced. Support product development activities, including design control, risk management, sterilization, biocompatibility, and design transfer/process validation. Oversee manufacturing quality activities at contract manufacturers, ensuring compliance with product specifications and regulatory requirements. Develop and review test protocols and reports for design verification and process validation. Proactively ensure compliance with ISO 13485, 21 CFR 820, and other applicable quality standards and regulations. Contribute to risk management activities, including DFMEA, PFMEA, and product biological risk assessments. Use post-market data to enhance risk management programs and support failure investigations. Assist in supplier qualification, internal audits, and third-party audit preparations. Provide insights and metrics for management review. Qualifications: Bachelor's degree in engineering or a related field. 5+ years of experience in the medical device industry, with a focus on quality engineering and design. Strong understanding of ISO 13485, ISO 14971, and 21 CFR 820. Skilled in risk evaluation and decision-making. Proficient in interpreting technical documentation and mechanical drawings. Professional and collaborative team player with excellent interpersonal skills.

***No 3rd party candidates will be considered*** Title: QA Engineer Salary: 80k-115k target - Based on experience Setting: Onsite Designs and manufactures industrial-grade computer systems, including SBCs, embedded systems, network and security appliances, and more. Prefer candidates in Computer Hardware manufacturing ideally, exp w/ ISO audit is required. 9001 ideal but also open to other ISO guidelines MUST HAVE: Mandarin speakers are ideal, but we will also consider others like Cantonese, Malay, Thai, Vietnamese, and Tagalog. DUTIES AND RESPONSIBILITIES Promote and Enforce company ISO standard to ensure that targets are achieved Collaborate with all departments and quality team to ensure all staffs are working in compliance with Quality Management System regulation for ISO certification / audit Ensure compliance with national and international standards and legislation Review documents to ensure develop and deploy products meet all phrases of product development documentation per ISO procedure Ensure continuous improvement within the quality control systems and company culture Conduct routine audits on an ongoing basis for quality improvement and complete annual schedule internal audit Lead and reporting finding to the management team for quality investigation with corrective and preventive action report and closure Manage calibration program meet requirement Preparing reports by collecting, analyzing and summarizing information and trends Manage and work according to deadlines to meet company goals Validates quality processes including IQ, OQ, and PQ Performs other duties as assigned REQUIREMENTS Entry level, experience in a quality ISO standards and management role in manufacturing is a plus Requirement to work with ISO audits and Customer Audits Product Regulatory Audits for example UL, BV, SGS, CCC, CSA, Metlab Experience implementing manufacturing QA concepts such as Lean, Six-Sigma, and 5S Equipment's Calibration and Maintenance prefer Ability to handle multitasking within a high-pressure work environment Excellent written and verbal communication skills and ability to work as part of a team to support external and internal Customers. Excellent analytical and problem-solving skills Proficient with Microsoft office suite or related software

Major Responsibilities: Responsible for all aspects of assigned Program as Quality Engineer, including internal quality performance objectives, customer interface, program IPT (integrated product team), and program supplier quality support. Major Responsibilities: Schedules and maintains milestones and timeline tracking for key objectives. Performs Preliminary Reviews of DMRs and evaluates in-process rejections via QA Process procedures for Non-conforming Material and MRB Activity. Performs drawing control and CCB review activities for new and revised documents, ensuring customer notification of all changes. Performs Product Sell-Off included final work order test data package review prior to shipment to ensure product performance is within specified standards. Ensures Programs supplier quality issue resolution through coordination of resources and support of QC, Purchasing and Engineering groups. Interface with various company depart ments to assist in resolve quality problems and provide information to support ISO/AS9100 requirements Interfaces with customers, vendors, and various company depart ments to resolve quality problems and provide information and may perform internal and/or supplier surveys and audits. Performs analysis of manufacturing performance and prepares reports for management on quality trends and actions to improve. Ensures training of subordinate employees in quality or other required functions. Leads interdisciplinary teams to address quality problems via formal Customer, Internal or Supplier corrective and preventive actions. Presents oral and visual presentations during technical meetings Supports and implements added scope objectives and activities outlined by Quality Director. Education/Experience/Training: BS / MS degree, with a technical emphasis preferred, with 8 years of related QA experience... In lieu of a degree, 10-12 years consistent Quality Engineering "Hands-on" experience at a Senior Level. Preferred one or more certifications in Quality Sciences such as Lean, 5S, Six Sigma, ISO/AS9100, SPC, ASQ certified engineer/manager/auditor, or similar. Excellent communication skills and experience in oral and written presentations. Must have interfaced or performed as a liaison to the customer for QA - ie Experience in this role with DCMA or other government agencies preferred. Must be familiar with and have experience in design phase activities, manufacturing test and evaluation, working with electromechanical systems and mechanical hardware. Ability to develop and implement projects requiring interface with design engineers, quality engineers, and supplier and subcontract technical personnel. Should be familiar with government and commercial specification for Quality Assurance, and Test and Evaluation. Must be computer literate and have hands-on experience with current MS Office Software utilities and application programs. Additional Requirements: Must be able to obtain and maintain a Security Clearance, with potential to handle classified data. Flexible to work varied shifts, overtime, weekends and travel on occasion. Able to occasionally complete manual activities as part of job including stoop, bend, kneel, and squat and manual dexterity. Must have sufficient vision to see relative positions of small parts and able to discern symmetry and proper alignment. May be required to move items 25 pounds for distances of up to 25 feet. Must wear appropriate personal protective equipment as necessary. Based on job duties, and need to visit different areas within the company, may be exposed to fumes, dust, toxic or caustic chemicals (well below OSHA and ACGIH exposure guidelines), outdoor weather, moving mechanical parts and/or be part of a hearing conservation program due to noise levels around certain equipment. In compliance with pay transparency requirements, the salary range for this role is $76,500 - $142,500. This is not a guarantee of compensation or salary, as the final offer amount may vary based on factors including but not limited to experience and geographic location. Fisica Inc. also offers a variety of benefits, including relocation stipend, 401(k), PTO, EAP, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, and schedule type.

Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our mission is to solve environmental compliance problems for industrial and governmental/infrastructure facilities. We are a growing and dynamic organization of highly respected professionals. Yorke Engineering, LLC has assisted over 1,400 client organizations with their Air Quality and Environmental Compliance, Engineering, and Permitting needs. Our philosophy is to efficiently help government and industrial customers with the complex array of environmental laws and regulations. From simple permits to complex agency negotiations, from small companies to the largest of California's organizations, Yorke successfully solves our clients' Air Quality and Environmental challenges. Our team has over 1,000 years of combined environmental experience and consists of engineers and scientists that specialize in Air Quality, Waste, Water, CEQA, Safety, and Industrial Hygiene. We are looking for a sharp Air Quality Engineer/Scientist (Environmental Permitting and Compliance) to join our team in Northern CA. This is a full-time position at 40 hours per week from one of our Northern CA offices (Berkeley, San Francisco, or San Jose) during our normal business hours. We offer competitive salaries, a full benefits package including Paid Time Off, Holidays, Full Medical/Dental/Vision, along with a 401k program with a generous company match. Position Summary: The Air Quality Engineer/Scientist (Environmental Permitting and Compliance) performs professional engineering work, leading and executing the compliance and permitting functions in relation to Air Quality Regulations and Compliance. This candidate will be reviewing processes and equipment, analyzing permit-related technical and regulatory issues, and communicating those analyses within Yorke, the client organization, with government agencies and with the public at large. The work is challenging, broad in scope, and variable from project to project. The position involves effective communication, decision-making, and time management. The candidate performs other duties as required or assigned. The candidate's experience and qualifications we are seeking include: 5-15+ years of work experience in the Air Quality and/or Environmental industry in an engineering role (preferably in a consulting environment); Experience in the environmental services industry focusing on Air Quality services: Process and equipment review; Air quality permitting under BAAQMD, SCAQMD, SJVAPCD and other Air Districts, including Title V Permitting; RECLAIM implementation and reporting; Annual Emissions Reporting; Air Dispersion Modeling; Air Quality Assessments including Data Analysis and Emission Inventories; General Air Quality Compliance for facilities in CA. Ability to be an active team member on project teams towards project completion within project scope, budget and schedule and ensure quality work product and deliverables; Ability to work with clients, staff, and regulators through effective communication and expertise by fostering a collaborative environment without losing focus of quality; Proven track record or desire to engage in successful regulatory work in dealing with the SCAQMD, BAAQMD, SJVAPCD, EPA, CARB and/or other similar regulatory agencies; Experience or desire to work on-site at client facilities; Prepare reports and submissions in timely manner; Experience with handling highly technical data and technical data interpretation; Highly motivated to continue working in Air Quality environmental field and expand their knowledge and experience; CA Regulatory/Compliance experience is required. Job Requirements: B.S or M.S. degree in Chemical Engineering, Environmental Engineering, or Mechanical Engineering, or other relevant technical degrees from an accredited college (minimum GPA of 3.0); Ability to work collaboratively in a team fashion, handle several projects at once, prioritize work, and work efficiently; Desire to learn or developing technical expertise in environmental rules and regulations; Excellent oral and written communications skills; Experience in conflict resolution and crisis management; Track record of successful analysis, interpretation, and application of rules and regulations towards practical solutions; Ability to think critically and develop solutions; Software Knowledge: Strong Microsoft Excel, Word, Outlook, and Powerpoint skills (required); Microsoft 365 Applications, including Sharepoint (a plus) EIT, CPP or P.E. Certification (a plus).

Hello, One of my clients is currently looking for a Development Quality Engineer. If you're interested or if your skills align with the role, please share your updated resume with me at *********************. Role: Development Quality Engineer Location: Pleasanton, CA Duration: 12 Months Note: NO C2C Key Responsibilities: Project Management: Managing projects related to new production equipment, process improvements, cost reductions, and supporting new product introductions. Collaboration: Working with outside consultants, vendors, and the medical community. Ticket Management: Helping with troubleshooting Tier II and III tickets, clinic creation requests, and support for EHR setup. Documentation and Compliance: Ensuring compliance with Abbott's, FDA, and ISO design controls, and supporting all divisional initiatives. Testing & Validation: Developing test plans for production and staging deployments, assisting with validation testing for medical devices and mobile applications. Incident Management: Supporting incident management for connectivity and production issues post-deployment. Required Qualifications: Bachelor's Degree in engineering, product support, IT, telecommunications, or related field. 0-3 years of experience, preferably in testing and validation for production/staging deployments. Strong analytical, problem-solving, and project management skills. Strong verbal and written communication skills. Ability to multitask, prioritize, and meet deadlines. Preferred Qualifications: Medical device experience is preferred. Strong organizational skills with attention to detail. Experience in a cross-divisional, geographically diverse business environment is a plus.

Corporate Background Gridtential Energy is a Silicon Valley energy storage startup in the process of commercializing its proprietary Silicon Joule Technology. Silicon Joule incorporates solar silicon wafers & processing techniques into a novel bipolar battery architecture. This innovative approach to battery design combines the traditional benefits of lead acid batteries - low cost, robustness, and safety - with the recharge performance and life cycle benefits usually associated with lithium-ion batteries. The result is a high-performance and low-cost energy storage platform attracting attention in major applications including the automotive, energy storage, and industrial markets. Gridtential's business model is built upon a capital-light design, supply, and license approach that partners, rather than competes, with the world's leading battery manufacturers. We start with our OEM partners to optimize our technology around their applications. Next we leverage our expertise in silicon processing techniques through a high-volume Asian supply chain. Meanwhile, battery assembly expertise is jointly developed with our highly experienced licensed partners who handle OEM fulfillment. Commercialization efforts are currently underway worldwide with several global manufacturers and joint pilot production has already been initiated with one of Gridtential's licensed partners. These collaborative partnerships have brought together Silicon Valley thinking and a century's worth of manufacturing expertise. Gridtential is staffed with a team of serial entrepreneurs, experienced managers, creative engineers, and master technicians. We treasure an open, direct, and politic-free culture that focuses on high productivity and collaborative achievement of ambitious goals in an enjoyable working environment. Come help us change the landscape of energy storage and create a cleaner, more efficient energy future for all. Role Background Gridtential has entered an exciting commercialization phase for its launch product and the team is growing. The Engineering Technician will play a key role in helping both the Engineering and the Operations teams to be successful. This role will have a broad opportunity to impact the organization in a hands-on way across multiple different areas. From ongoing fundamental R&D of next-generation products to process development for commercialization efforts, you will have the opportunity to contribute at every level. The Engineering Technician will have a hands-on role helping prepare Gridtential's proprietary silicon materials, performing battery assemblies, tearing down batteries at end of life, and working with the engineering team to validate new ideas. Additionally, operating with a high level of autonomy, you will review experimental requests from the engineering team and plan their execution, keep a regular inventory of materials in the lab, manage shipping/receiving of samples, and communicate problem areas back to the broader team. Gridtential uses a structured, schedule-driven product development approach and the Engineering Technician will work with a team of engineers to achieve clearly defined performance targets on aggressive timelines. The ideal candidate will have prior experience in battery technology or the automotive industry. They will have a well-documented history of creative problem solving and cross-functional collaboration. Responsibilities Hands-on assembly of batteries (multiple types and voltages) Preparation of battery materials for engineering experiments Preparation of chemical solutions, weighing of reagents, recording data, and following written procedures in support of engineering experiments Hands-on co-development of battery assembly processes with the engineering team QA and rework of incoming materials (including silicon wafers) and assembled battery products Hands-on collaboration with engineering team to trial new battery designs or preparation processes - will be expected to provide feedback to the engineering team regarding successes/failures of proposed designs Utilize drill press, band saw, belt sander, Dremel tool, and other light-duty fabrication tools to create and/or modify fixtures and parts Hands-on battery teardown operations, working in collaboration with the engineering team to identify failure modes and brainstorm fixes Oversee shipping/receiving of samples out of Gridtential's Santa Clara lab Maintain order and cleanliness of equipment and facilities in Santa Clara lab, maintain inventory of lab supplies, and ensure all safety precautions are being followed Interface with local vendors and shops to order components as needed to complete tasks Skills and Knowledge Demonstrated ability to assemble complex assemblies Mechanical fabrication skills - comfortable using hand and power tools Prior chemistry lab experience a plus Track record of finding creative solutions to solve problems Familiarity with battery and/or fuel-cell construction a plus Strong troubleshooting skills Demonstrated ability to work independently, must be a self-starter Ability to manage shifting priorities and workloads Excellent interpersonal skills and ability to work within a team Proficient with Microsoft Office Mandarin language capability a plus Qualification and Experience 1+ years of engineering technician experience OR related degree Must be eligible to work in this country for any employer What we offer Comprehensive medical, dental and vision plans for you and your dependents 401(k) Retirement Plan Competitive Compensation Training and development programs Stocked kitchen with snacks and beverages Collaborative culture Work-life balance and generous paid time off

Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. As a team, we've launched two satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $500 million from top global investors, and recruited a team of over 300 world-class engineers. We all work out of our (legendary) San Francisco office, which was once used to build ships during the World Wars. Our satellites, which operate from geostationary orbit (GEO), weigh only 400 kg and utilize a proprietary software-defined radio payload. Each satellite can connect over two million people, and we're very excited for the impact we'll soon have in the Philippines, Peru, Mexico, and more! Backed by substantial funding and a passionate, collaborative team, we offer a rewarding work environment where you'll learn and make a significant impact, no matter where you are in your career. Apply and join us on our journey towards global connectivity! Production Quality Inspector As a Production Quality Inspector, you are responsible for being the last line of defense in assuring mission success. You will work with the most cutting edge MicroGEO satellite technology and perform inspections in several workcenters to verify our hardware meets the highest level of quality. The ideal candidate is self-driven, extremely detail oriented, and seeks a highly cross functional dynamic environment. Responsibilities Perform in-process inspection and final verification of flight hardware to drawing, process specifications, and work order requirements supporting multiple work centers (assembly, integration, wire harnessing, or test) Identify, document, and verify resolution of production and test non-conformances in accordance with prescribed procedures and pursue corrective action as required Interface with engineering and production to communicate and help resolve nonconforming issues Independently perform verifications and document results in a clear, precise, and complete manner Support quality management system policies and procedure documentation, assess compliance to company and industry standards, initiate and lead continual improvement and lean manufacturing initiatives Perform other related duties, as assigned, for the purpose of ensuring an efficient and effective work environment Requirements 3+ years of inspection experience in an aerospace, military or manufacturing environment Substantial knowledge of the control of nonconforming hardware, failure/root cause analysis, corrective and preventive action processes Experience reading and interpreting design drawings and CAD models Experience with performing electronic testing and inspection using portable measuring devices and lab equipment (microscopes, testers, scopes, etc) Excellent communication (written and verbal) and teamwork skills Ability to work independently with a strong work ethic, be innovative, detail oriented, possess initiative, and team oriented Willing and able to work overtime and/or weekends as required Bonus Associate degree or higher in quality, engineering, or related field Knowledgeable with ISO 9001/AS9100 quality management systems Experience inspecting solder, crimping, conformal coating, staking, and surface mounted devices in accordance with IPC-J-STD-001 or IPC-A-610 standards Wire harness experience in accordance with IPC-A-620 standards Six Sigma Yellow/Green Belt certified What we offer: All our positions offer a compensation package that includes equity and robust benefits. Base pay is a single component of Astranis's total rewards package, which may also include equity in the form of incentive stock options, high quality company-subsidized healthcare, disability and life insurance benefits, flexible PTO, 401(K) retirement, and free on-site catered meals. Astranis pay ranges are informed and defined through professional-grade salary surveys and compensation data sources. The actual base salary offered to a successful candidate will additionally be influenced by a variety of factors including experience, credentials & certifications, educational attainment, skill level requirements, and the level and scope of the position. Base Hourly Pay $30 - $40 USD U.S. Citizenship, Lawful Permanent Residency, or Refugee/Asylee Status Required (To comply with U.S. Government space technology export regulations, applicant must be a U.S. citizen, lawful permanent resident of the United States, or other protected individual as defined by 8 U.S.C. 1324b(a)(3)) Our mission and our products are meant to connect the world and everyone in it, regardless of gender, race, creed, or any other distinction. We believe in a diverse and inclusive workplace, and we encourage all people to join our team and bring their unique perspective to help make us stronger.

The successful candidate will be responsible for assembling, testing, and maintaining battery systems, ensuring high-quality standards are met throughout the manufacturing process. This role requires a strong technical background, attention to detail, and the ability to work effectively in a fast-paced production environment. This will be a contract role with a duration of 3 to 6 months. Responsibilities: Assemble battery systems and related components according to engineering specifications and standard operating procedures (SOPs). Operate assembly equipment, tools, and machinery. Perform precision assembly tasks, including wiring, soldering, and mechanical assembly. Follow production schedules and meet daily, weekly, and monthly production targets. Conduct electrical and mechanical tests on battery systems to ensure functionality, safety, and compliance with quality standards. Inspect and verify the quality of assembled products, identifying defects or issues and taking corrective actions. Record test data, maintain accurate production logs, and report any discrepancies via ticketing systems. Minimum Qualifications: High school diploma or equivalent; associate degree or technical certification in a relevant field is preferred. Proven experience in manufacturing, preferably in battery systems or a related industry. Strong understanding of electrical and mechanical assembly processes. Proficiency in using hand tools, power tools, and testing equipment. Familiarity with safety standards and practices in a manufacturing environment. Ability to read and interpret technical drawings, schematics, and assembly instructions. Excellent attention to detail and a commitment to producing high-quality work. Strong problem-solving skills and the ability to troubleshoot technical issues. Ability to work independently as well as in a team-oriented environment. Flexibility to work shifts, including evenings or weekends, as required. Eligible to work in the U.S. Compensation: $28.00/hr to $30.00/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

We are seeking a Quality Inspector in the food industry to join a client in Hayward. The role is with a health and nutrition services client. This is a temp-to-hire position. This is a 100% onsite position. Hours are Monday - Friday 8:00 am - 4:30 pm with a starting pay of $25-$28 an hour. Job Duties: Coordinate with client lab to ensure that specifications are accurate before being sent for testing. Verify invoices match test prices. Manage and track QC tests after they are received and sending to the lab. Obtain PO's from accounting for tests. Coordinate tests. Be the internal point of contact to relay test results. File reports on QC. Communicate with vendors on tests and maintenance. Follow lab safety practices. Organize samples. Requirements: Bachelor's Degree preferred or Associate's Degree Chemistry background a plus. Strong MS Office and computer skills. Ability to lift up to 25 lbs. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Astranis is on a mission to bridge the digital divide by connecting the four billion people worldwide who currently lack internet access. We're doing this by building the next generation of smaller, more cost-effective spacecraft to bring the world online. As a team, we've launched two satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $500 million from top global investors, and recruited a team of over 300 world-class engineers. We all work out of our (legendary) San Francisco office, which was once used to build ships during the World Wars. Our satellites, which operate from geostationary orbit (GEO), weigh only 400 kg and utilize a proprietary software-defined radio payload. Each satellite can connect over two million people, and we're very excited for the impact we'll soon have in the Philippines, Peru, Mexico, and more! Backed by substantial funding and a passionate, collaborative team, we offer a rewarding work environment where you'll learn and make a significant impact, no matter where you are in your career. Apply and join us on our journey towards global connectivity! Production Quality Inspector As a Production Quality Inspector, you are responsible for being the last line of defense in assuring mission success. You will work with the most cutting edge MicroGEO satellite technology and perform inspections in several workcenters to verify our hardware meets the highest level of quality. The ideal candidate is self-driven, extremely detail oriented, and seeks a highly cross functional dynamic environment. Responsibilities Perform in-process inspection and final verification of flight hardware to drawing, process specifications, and work order requirements supporting multiple work centers (assembly, integration, wire harnessing, or test) Identify, document, and verify resolution of production and test non-conformances in accordance with prescribed procedures and pursue corrective action as required Interface with engineering and production to communicate and help resolve nonconforming issues Independently perform verifications and document results in a clear, precise, and complete manner Support quality management system policies and procedure documentation, assess compliance to company and industry standards, initiate and lead continual improvement and lean manufacturing initiatives Perform other related duties, as assigned, for the purpose of ensuring an efficient and effective work environment Requirements 3+ years of inspection experience in an aerospace, military or manufacturing environment Substantial knowledge of the control of nonconforming hardware, failure/root cause analysis, corrective and preventive action processes Experience reading and interpreting design drawings and CAD models Experience with performing electronic testing and inspection using portable measuring devices and lab equipment (microscopes, testers, scopes, etc) Excellent communication (written and verbal) and teamwork skills Ability to work independently with a strong work ethic, be innovative, detail oriented, possess initiative, and team oriented Willing and able to work overtime and/or weekends as required Bonus Associate degree or higher in quality, engineering, or related field Knowledgeable with ISO 9001/AS9100 quality management systems Experience inspecting solder, crimping, conformal coating, staking, and surface mounted devices in accordance with IPC-J-STD-001 or IPC-A-610 standards Wire harness experience in accordance with IPC-A-620 standards Six Sigma Yellow/Green Belt certified What we offer: All our positions offer a compensation package that includes equity and robust benefits. Base pay is a single component of Astranis's total rewards package, which may also include equity in the form of incentive stock options, high quality company-subsidized healthcare, disability and life insurance benefits, flexible PTO, 401(K) retirement, and free on-site catered meals. Astranis pay ranges are informed and defined through professional-grade salary surveys and compensation data sources. The actual base salary offered to a successful candidate will additionally be influenced by a variety of factors including experience, credentials & certifications, educational attainment, skill level requirements, and the level and scope of the position. Base Hourly Pay $30 - $40 USD U.S. Citizenship, Lawful Permanent Residency, or Refugee/Asylee Status Required (To comply with U.S. Government space technology export regulations, applicant must be a U.S. citizen, lawful permanent resident of the United States, or other protected individual as defined by 8 U.S.C. 1324b(a)(3)) Our mission and our products are meant to connect the world and everyone in it, regardless of gender, race, creed, or any other distinction. We believe in a diverse and inclusive workplace, and we encourage all people to join our team and bring their unique perspective to help make us stronger.

Must Have: 3+ years' experience as a Quality Control Inspector for Mechanical 3+ years of experience with ASME B31 piping codes, industrial and commercial construction, fabrication, welding, non-destructive testing Certification Requirement: AWS QC-1 as a Certified Welding Inspector (CWI) Plus: Mechanical - Commercial Certification AWS D1.1, D1.6, ASME Section IX, ASME B31 Piping Codes Experience Semiconductor or Biopharmaceutical Processing Equipment (BPE) and piping systems Day to day: A client of Insight Global is looking for a Quality Control Inspector to join their team. This individual will represent the company for pipe and equipment installation, welding inspection and oversight of subcontractor installation and quality. The QA QC Inspector will participate in the General Contractors project quality program documenting installation activities. Plans and conducts the analysis, inspection, design, test, and integration to assure the quality of assigned product or component. Performs quality engineering reviews of design documentation for compliance with stated requirements, including vendor quality manuals and company quality records. Reviews all purchased products or components and provides input to the decision of whether the product has been vetted for future purchases from the vendor. Documents data obtained during all quality assurance activities, consistent with company policies, codes and procedures. Communicates significant issues or developments identified during quality assurance activities and provides recommended process improvements to management. Prepares reports to communicate involvement and results of quality assurance activities. Maintains a working knowledge of codes and specifications for current industry quality standard Annual Compensation: $125,000 - $140,000 Exact compensation may vary based on several factors, including skills, experience, and education.