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Quality Technician Jobs in Manteca, CA

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Quality Technician
Senior Quality Engineer
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Quality Assurance Technician
Process Technician
  • Quality Specialist

    DSJ Global

    Quality Technician Job 46 miles from Manteca

    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: $80k-85k + Bonus + Benefits If you are interested, don't hesitate to apply!
    $70k-112k yearly est. 8d ago
  • Quality Inspector, Machining

    Astranis Space Technologies 3.9company rating

    Quality Technician Job 48 miles from Manteca

    As a team, we've launched five satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $750 million from top global investors, and recruited a team of over 400 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. As a Quality Inspector, you will be tasked with the challenge of analyzing and inspecting precision machined parts here at Astranis. Astranis is producing some of the most capable and compact geostationary satellites ever flown, which demand complex geometry and tight tolerances to achieve the mission performance and life targets. If you are ready to take precision to the next level, this job is for you! This role will be a dedicated quality person in the machining and development operations group, and will work closely with the head of machining to ensure the highest quality controls for parts made both internally and externally, as well as performing key measurements on the satellite and owning quality processes across the business. The ideal candidate has extensive precision/dimensional inspection experience using an array of tools both manual and automated, can maintain quality processes, and can effectively check all required measurements. Role Inspect all mechanical parts built in the Astranis machine shop and at various suppliers, for both flight and development use, and ensure zero quality escapes to the production line. Program and operate the CMM and Faro measurement equipment for both component inspection and satellite integration-level measurements. Follow work orders to document part manufacturing and inspection processes, including part marking and traceability. Conduct precision tooling calibrations on a scheduled basis. Create issue tickets and templates for nonconforming hardware and work with engineering to ensure speedy resolution, including performing containment of other discrepant hardware as needed. Work with machinists to improve the machining process for more accurate part manufacturing. Work with the inventory team to follow the process for incoming quality control of machined components. Partner with engineering to develop new processes such as fabrication or cleaning, to ensure the right quality controls are built-in from the start. Maintain a system for tracking metrology and manage the on-time calibration of tools across the entire factory. Give feedback via reports and graphics on part tolerance and measured values. Set up and maintain a request/priority system for inspections, tool calibration, etc. to keep the business informed of status, progress, and blockers. Conduct regular quality reviews to communicate performance, challenges, and opportunities to improve for both internal machine shop and suppliers. Requirements 2+ years in a quality inspector/CMM programmer role focused on precision/dimensional inspection of machined parts. 2+ years experience reading and manipulating CAD models and engineering drawings including Geometric Dimensioning and Tolerancing (GD&T) language. 2+ years programming and operating Coordinate Measurement Machine (CMM). Proficient with all measurement tools required to inspect machined hardware, such as calipers, micrometers, pins, and other gauges. Fast-paced, self-directed, and able to execute with minimal direction. Bonus Mitutoyo MCOSMOS programming. Faro arm measurement. Knowledge of manufacturing execution system (MES) and warehouse management system (WMS) software packages. Trained in 5S area setup and maintenance. Precision cleaning and part marking. Tool calibration experience. 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 $40 - $50 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.
    $40-50 hourly 9d ago
  • Senior Quality Systems Specialist (Document Control)

    Germer International-Pharmaceutical Recruiting

    Quality Technician Job 44 miles from Manteca

    Our client is seeking a Quality Assurance Specialist who will be responsible for maintaining product quality and compliance by working closely with departments such as manufacturing, R&D, and regulatory affairs. This role involves reviewing documentation, leading audits, investigating deviations, overseeing project initiatives, managing document workflows, and offering back-up support for quality control functions. Qualifications: Bachelor's in life sciences preferred 7+ years of quality assurance experience Expertise in conducting audits, inspections, and assessments Proficient in quality tools (e.g., Document Control, CAPA, Deviations, Audit, SPC) Strong understanding of GMP/ISO regulations and quality management systems Experience in the life sciences, pharmaceuticals Familiarity with eQMS, ERP systems, and other information systems Key Responsibilities: Oversee CAPAs and document control Conduct internal audits and support external audits Review and approve quality documentation (e.g., SOPs, specifications) Ensure compliance with regulatory standards Investigate deviations and implement corrective actions Support the development and maintenance of quality systems Provide training on quality procedures and best practices Participate in risk assessments and quality improvement initiatives Track corrective and preventive actions to ensure timely resolution Support data analysis, reporting, and vendor audits Maintain accurate quality documentation and ensure compliance
    $72k-96k yearly est. 3d ago
  • Cathode processing technician opening in San Jose

    Ultimate Staffing 3.6company rating

    Quality Technician Job 48 miles from Manteca

    Ultimate Staffing is seeking a Cathode Processing Technician for our client in San Jose. This is a 100% onsite, temp to perm position with a schedule of Monday-Friday 2:30pm-11:00pm and a starting pay of $35-$40 an hour based on experience. *** THIS IS NOT AN ENTRY LEVEL ROLE. CANDIDATES WITHOUT RELEVANT EXPERIENCE WILL NOT BE CONSIDERED *** Responsibilities: - Document and report experimental details to achieve reproducible, high-quality data in a timely and professional manner - Follow SOPs and keep accurate, detailed laboratory records and shift reports - Document daily experiments and communicate completion status using MS Office applications - Work closely with engineers and technicians to implement improvements and maintain a reliable process - Assist in maintaining supplies inventory and advising on supply needs - Troubleshoot basic issues and/or seek help for experimental issues by coordinating with engineers, facilities, or maintenance personnel Requirements: - Typically requires a minimum of 5 years of related experience - Ability to perform work in a dry room, and glovebox that requires the use of fine motor skills for extended periods of time, standing, reaching and twisting motions with hands, and lifting up to 25 lbs. - Phenomenal attention to details; follow procedures to efficiently run equipment and handle chemicals safely. - Clear written and verbal skills to logically communicate observations and thought processes. - Basic computer skills to accurately record and analyze data Preferred: Experience of working in glove box and/or dry room. 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.
    $35-40 hourly 7d ago
  • Quality Engineer

    Neuspera Medical Inc. 3.9company rating

    Quality Technician Job 48 miles from Manteca

    LOCAL CANDIDATES ONLY 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
    $100k-125k yearly 10d ago
  • Quality Assurance Technician

    Planet Pharma 4.1company rating

    Quality Technician Job 48 miles from Manteca

    $31 - $35 per hr Shift: M-F 8:30-5 4-5 month contract - this role will NOT extend as the site is closing REQUIRED: Min of 2+ years of manufacturing QA experience Experience with finished product testing, inspection, batch record review/product release - must have all biotech, pharma, medical device industry experience highly preferred SCOPE: The Quality Assurance Technician is located at and supports the Hayward, CA manufacturing site. PRIMARY RESPONSIBILITIES: • Support manufacturing by performing duties such as incoming, in-process and final inspections, DHR review and completion, product release, etc. • Authorize release of material, subassembly and product. • Prevent release of suspect or known nonconforming products and materials. • Ensure all activities are performed in accordance with Quality System requirements, work instructions and regulatory requirements. • Follow detailed process steps without deviation. • Initiate deviations (NCR) as needed upon occurrence and collect information for investigation. • Collaborate with other functional teams to identify, investigate and resolve product quality issues. • Conduct training to Quality Systems processes as defined within the learning management system.
    $31-35 hourly 15d ago
  • Senior Quality Engineer

    Ace Partners 4.3company rating

    Quality Technician Job 48 miles from Manteca

    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.
    $150k-160k yearly 15d ago
  • Quality Engineer, Senior Quality Engineer

    Advanced Bifurcation Systems Inc.

    Quality Technician Job 31 miles from Manteca

    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). Responsibilities The range of responsibilities includes but not limited to developing and implementing quality standards, monitoring and analyzing quality performance, inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met; collaborating with cross-functional teams to develop and implement controls and drive improvements, ensuring that workflows, processes, and products comply with safety regulations, investigating and troubleshooting product or production issues, developing corrective actions, solutions, and improvements; reviewing specifications, and processes. The senior quality engineer may assume leadership role leading projects and teams, even strategizing, championing, motivating and ensuring all teams receive the appropriate information and guidance. Technical Develop and maintain quality systems and documentation in compliance with FDA, ISO, and EUMDR requirements. Lead and/or support on-time completion of design control deliverables for both new product introductions and design change projects. Support design verification/validation planning and execution, including any cross-functional investigation and resolution activities. Ensure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps. Lead risk management activities from product concept through commercialization. Support Product development activities and design transfer into manufacturing. Support Manufacturing Engineering in the creation, release and maintenance of DHR/LHR, bills of material, and specifications for manufacturing. Assist in the selection, qualification, and assessment of new suppliers based on established procedures. Conduct supplier audits to evaluate their capabilities, processes, and quality management systems. Develop establish and maintain periodic reviews with suppliers on their performance(scorecards), and improvement or corrective action plan(s). Support nonconforming material investigation and disposition activity, participate in weekly MRB meetings, follow-up on supplier issues. Assist with maintenance of calibration system. Perform incoming inspection review and disposition of product components and subsystems. Assist in investigations of quality issues arising from product complaints, CAPAs, and non-conforming reports. Utilize problem solving tools to analyze and identify root causes and implement corrective actions. Actively participate in the Doc-Control process. Support the Environmental monitoring process. Initiate /approve validation protocols and reports (IQ, OQ, PQ). Initiate /approve process validation protocols and reports. Other duties and responsibilities as mutually agreed. Leadership/Communication/Compliance Be an advocate for quality and create a culture of quality. Be responsible in whole or in part for the effective manufacture of medical devices, compliance with internal policies/procedures and applicable regulations, and the efficient execution of related activities. Must be able to work under pressure and meet deadlines, while maintaining a positive attitude and providing exemplary customer service to both internal and external customers. Adhere to the Company's Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. Act as the QA representative in cross-functional team meetings, MRB, new product introductions, and supplier quality meetings. Make decisions and propose solutions based on calculated risks identified through data analysis.Process Customer Complaints and manage customer replies Champion continuous improvement through CAPA system, handling of complaints, analyzing key performance indicators. Support activities associated with Sterilization and Biocompatibility Assist in training personnel to processes associated with design and development and manufacturing. Attributes Attention to Detail and Cognitive Skills working on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Candidate must be highly motivated with excellent communication skills and proven ability to work as part of a team. Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers. Strong documentation capability for protocol and report generation and review. Ability to work ina rapidly changing and evolving environment. • Prior start-up experience is a plus. Physical Demands Business travel from 0% - 25%. Requires some lifting and moving of up to 40 pounds. Required to frequently stand, walk, sit, and use a computer for extended periods. Specific vision abilities required by this job include, close/distant vision and depth perception. Position also requires use of Personal Protective Equipment as needed
    $112k-152k yearly est. 10d ago
  • Senior Quality Engineer

    Lumicity

    Quality Technician Job 48 miles from Manteca

    Are you passionate about advancing medical technology and improving patient outcomes? Join a rapidly growing medical device company that's revolutionizing healthcare through innovative solutions. Your Impact As a Senior Quality Engineer, you'll be at the forefront of ensuring product excellence and regulatory compliance for groundbreaking medical technologies. Your expertise will directly contribute to products that enhance patient care and safety. What You'll Do Drive quality initiatives across product development and manufacturing processes Lead FMEA, CAPA, and root cause analysis investigations Collaborate with cross-functional teams to implement quality management systems Ensure compliance with FDA regulations and ISO standards Develop and maintain quality documentation and procedures Mentor junior team members and contribute to continuous improvement initiatives What You Bring Bachelor's degree in Engineering, Life Sciences, or related field 3+ years of quality engineering experience in medical devices/healthcare Deep understanding of FDA regulations, ISO 13485, and ISO 14971 Hands-on experience with quality tools (FMEA, CAPA, Six Sigma) Strong analytical mindset and problem-solving capabilities Excellence in communication and team collaboration Bonus Points CQE certification Experience with Class II or III medical devices Track record of implementing quality management systems Why This Role? Join a fast-growing company at the cutting edge of medical innovation Work with a collaborative team dedicated to improving healthcare Competitive compensation and comprehensive benefits package Career growth opportunities in a rapidly expanding organization Ready to Make an Impact? If you're excited about shaping the future of medical technology while ensuring the highest quality standards, we want to hear from you. Send your resume and a brief note about why you're interested to ********************* with the subject line "Senior Quality Engineer - San Jose." Lumicity is proud to represent leading innovators in the medical device industry. We are committed to diversity and inclusion in our recruitment process.
    $112k-152k yearly est. 15d ago
  • Quality Engineer

    The Ash Group

    Quality Technician Job 44 miles from Manteca

    ***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
    $87k-117k yearly est. 15d ago
  • Quality Engineer II or Senior Quality Engineer

    Cambridge Recruiters 4.4company rating

    Quality Technician Job 37 miles from Manteca

    QE II or Senior Quality Engineering job opportunity (Title Flexible) Company: Fast-growing Spinal Instrument & Implant medical device company 100-Person company with with multiple products on-market. They've been around 15+ years and sales have been very strong. They're adding 10 new Sales Reps to expand multiple markets across the US. It's a brand-new position (opening this week) and will be part of a small quality team: VP Quality, Sr. QE, QA Tech, Doc Control. Position will report to the VP. Job Focus: Manufacturing/Ops Quality & Quality Systems Engineering support. Continuous improvements, risk management, validations, internal & supplier quality audits, compliance, etc. Requirements & Job Info: BS or MS Engineering degree 3-6+ years Quality Engineering experience MUST HAVE: Medical Device experience Full-Time Permanent position, full benefits, stock options, etc. No H1B Candidates - must have US Work Authorization or be a US Citizen. Local Candidates only - no relocation assistance available. About me: 20 yrs recruiting experience for medical device companies *************************** Testimonials: *********************************************
    $123k-157k yearly est. 8d ago
  • Senior Quality Engineer

    Pivotal Systems 3.7company rating

    Quality Technician Job 44 miles from Manteca

    Job Title: Sr. Quality Engineer Company: Pivotal Systems The Quality Engineer will be responsible for Quality Assurance, Quality Control, and ISO 9001:2015 Quality Management Systems. This role ensures compliance with quality standards, leads audits, and drives continuous improvement initiatives across the organization. Key Responsibilities Led, implement and maintain ISO 9001:2015 Quality Management Systems. Perform QMS Internal Audits and lead External ISO 9001:2015 QMS Registration Audits. Maintain the Quality Manual and Policy. Monitor, track, and improve Quality Objectives/KPIs. Identify key QMS processes and their owners. Conduct Management Reviews in accordance with ISO 9001:2015 QMS requirements. Train team members on the ISO 9001:2015 QMS. Oversee Advanced Product Quality Planning for new products and product changes. Collaborate with the Design Team on design reviews, design verification, and design validation. Work with the Manufacturing and Equipment Teams to develop DFM, DFA, and/or DFX practices. Assist in equipment selection, verification, and validation within the scope of quality. Develop and maintain documented information systems, SOPs, and work instructions. Conduct Design of Experiments (DOE) for process development and validation. Develop and maintain Quality Control Plans, PFMEA, and Process Flow Charts. Perform Measurement System Analysis, calibration, and measurement system validation. Analyze Voice of the Customer (VOC) data and translate it into functional requirements and characteristics. Collaborate with Supplier and Customer Design Teams on DFMEA and DVPR. Understand Critical to Quality (CTQ) requirements and develop inspection gauges/poka-yokes. Develop inspection methods and improve product quality KPIs. Lead 8D problem-solving meetings to develop corrective and preventive actions. Assist in supplier selection, evaluation, and performance monitoring. Onboard new suppliers and support them in developing quality and capacity. Perform statistical analysis using JMP, including: Distribution Regression DOE Gage R&R ANOVA Control Charts Capability Analysis Initiate Six Sigma DMAIC projects to improve product quality. Monitor and train Quality Team members. Maintain and improve processes identified by the QMS. Qualifications & Certifications Education: Bachelor's degree in Engineering preferred. Experience: Minimum of 5 years in quality assurance and quality control. ISO 9001:2015 Lead Auditor Certification required. Skills and Knowledge: Significant problem-solving experience (DMAIC and 8D). Thorough knowledge of statistical techniques, including DOE and quality systems. Familiarity with 3Q6S methodologies. Proficiency in advanced quality tools such as APQP and FMEA. Advanced computer skills, including MS Office (Excel, PowerPoint, MS Project) and ERP systems. Strong presentation, facilitation, and interpersonal skills. Preferred Qualifications ASQ Six Sigma Green Belt or CQE certifications. Experience with Statistical Process Control (SPC). Six Sigma Black Belt certification (preferred).
    $111k-143k yearly est. 5d ago
  • Quality Inspector - Parachute Rigger

    U.S. Army 4.5company rating

    Quality Technician Job 48 miles from Manteca

    92R Parachute Rigger Seeking detailed oriented individuals to perform everyday tasks that save lives. You will build inspections skills as you become an expert in inspecting, packing, and repairing parachutes. Similar Jobs: Occupational Safety Inspector and Quality Control Inspector
    $38k-49k yearly est. 7d ago
  • Engineering Technician

    Insight Global

    Quality Technician Job 44 miles from Manteca

    Required Skills and Experience * -2+ years' experience as a technician, assembling and disassembling vehicle components, building test fixtures, and executing tests -Mechanically & electrically inclined (experience working with hand tools, etc) -Experience with CAN bus -Open to domestic travel Nice to Have Skills and Experience -Peak System Experience Job Description * Insight Global is looking for a Camera Systems Integration Technician to join one of our largest automotive clients in the Bay Area. This person will: -Execute tests: setup, perform inspections, conduct check ins, and retrofits -Document and report issues identified during tests or inspections -Collaborate with engineers to resolve mechanical & electrical issues discovered -Support engineers in instrumentation and data acquisition -Assist and learn from other technicians and engineers -Assemble & wire test fixtures This role can pay between $35-$40/hour depending on years of experience and skillset.
    $35-40 hourly 12d ago
  • Quality Inspector, Machining

    Astranis Space Technologies 3.9company rating

    Quality Technician Job 44 miles from Manteca

    As a team, we've launched five satellites into orbit, signed ten commercial deals worth over $1 billion in revenue, raised over $750 million from top global investors, and recruited a team of over 400 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. As a Quality Inspector, you will be tasked with the challenge of analyzing and inspecting precision machined parts here at Astranis. Astranis is producing some of the most capable and compact geostationary satellites ever flown, which demand complex geometry and tight tolerances to achieve the mission performance and life targets. If you are ready to take precision to the next level, this job is for you! This role will be a dedicated quality person in the machining and development operations group, and will work closely with the head of machining to ensure the highest quality controls for parts made both internally and externally, as well as performing key measurements on the satellite and owning quality processes across the business. The ideal candidate has extensive precision/dimensional inspection experience using an array of tools both manual and automated, can maintain quality processes, and can effectively check all required measurements. Role Inspect all mechanical parts built in the Astranis machine shop and at various suppliers, for both flight and development use, and ensure zero quality escapes to the production line. Program and operate the CMM and Faro measurement equipment for both component inspection and satellite integration-level measurements. Follow work orders to document part manufacturing and inspection processes, including part marking and traceability. Conduct precision tooling calibrations on a scheduled basis. Create issue tickets and templates for nonconforming hardware and work with engineering to ensure speedy resolution, including performing containment of other discrepant hardware as needed. Work with machinists to improve the machining process for more accurate part manufacturing. Work with the inventory team to follow the process for incoming quality control of machined components. Partner with engineering to develop new processes such as fabrication or cleaning, to ensure the right quality controls are built-in from the start. Maintain a system for tracking metrology and manage the on-time calibration of tools across the entire factory. Give feedback via reports and graphics on part tolerance and measured values. Set up and maintain a request/priority system for inspections, tool calibration, etc. to keep the business informed of status, progress, and blockers. Conduct regular quality reviews to communicate performance, challenges, and opportunities to improve for both internal machine shop and suppliers. Requirements 2+ years in a quality inspector/CMM programmer role focused on precision/dimensional inspection of machined parts. 2+ years experience reading and manipulating CAD models and engineering drawings including Geometric Dimensioning and Tolerancing (GD&T) language. 2+ years programming and operating Coordinate Measurement Machine (CMM). Proficient with all measurement tools required to inspect machined hardware, such as calipers, micrometers, pins, and other gauges. Fast-paced, self-directed, and able to execute with minimal direction. Bonus Mitutoyo MCOSMOS programming. Faro arm measurement. Knowledge of manufacturing execution system (MES) and warehouse management system (WMS) software packages. Trained in 5S area setup and maintenance. Precision cleaning and part marking. Tool calibration experience. 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 $40 - $50 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.
    $40-50 hourly 9d ago
  • Senior Quality Engineer

    Lumicity

    Quality Technician Job 44 miles from Manteca

    Are you passionate about advancing medical technology and improving patient outcomes? Join a rapidly growing medical device company that's revolutionizing healthcare through innovative solutions. Your Impact As a Senior Quality Engineer, you'll be at the forefront of ensuring product excellence and regulatory compliance for groundbreaking medical technologies. Your expertise will directly contribute to products that enhance patient care and safety. What You'll Do Drive quality initiatives across product development and manufacturing processes Lead FMEA, CAPA, and root cause analysis investigations Collaborate with cross-functional teams to implement quality management systems Ensure compliance with FDA regulations and ISO standards Develop and maintain quality documentation and procedures Mentor junior team members and contribute to continuous improvement initiatives What You Bring Bachelor's degree in Engineering, Life Sciences, or related field 3+ years of quality engineering experience in medical devices/healthcare Deep understanding of FDA regulations, ISO 13485, and ISO 14971 Hands-on experience with quality tools (FMEA, CAPA, Six Sigma) Strong analytical mindset and problem-solving capabilities Excellence in communication and team collaboration Bonus Points CQE certification Experience with Class II or III medical devices Track record of implementing quality management systems Why This Role? Join a fast-growing company at the cutting edge of medical innovation Work with a collaborative team dedicated to improving healthcare Competitive compensation and comprehensive benefits package Career growth opportunities in a rapidly expanding organization Ready to Make an Impact? If you're excited about shaping the future of medical technology while ensuring the highest quality standards, we want to hear from you. Send your resume and a brief note about why you're interested to ********************* with the subject line "Senior Quality Engineer - San Jose." Lumicity is proud to represent leading innovators in the medical device industry. We are committed to diversity and inclusion in our recruitment process.
    $112k-152k yearly est. 15d ago
  • Quality Inspector - Parachute Rigger

    U.S. Army 4.5company rating

    Quality Technician Job 48 miles from Manteca

    92R Parachute Rigger Seeking detailed oriented individuals to perform everyday tasks that save lives. You will build inspections skills as you become an expert in inspecting, packing, and repairing parachutes. Similar Jobs: Occupational Safety Inspector and Quality Control Inspector
    $38k-49k yearly est. 7d ago
  • QC Inspector - SMT

    Ultimate Staffing 3.6company rating

    Quality Technician Job 44 miles from Manteca

    Ultimate Staffing is seeking an SMT In Process Quality Control Inspector is located in Fremont and 100% onsite. This is a day shift position. Operate and maintain Surface Mount Assembly line. Read and work off documents and assembly drawings. Perform quality inspection. Operate solder printer, pic-n-place machines and equipment. Requirements: Prior equipment operating automated surface mount technology equipment. Ability to work off of assembly documents and assemble backplanes. Knowledge of automated assembly procedures. Ability to work off of mechanical drawings. High School Diploma or equivalent. 1-3 years prior experience. Desired Skills and Experience -Prior equipment operating automated surface mount technology equipment. -Ability to work off of assembly documents and assemble backplanes. -Knowledge of automated assembly procedures. -Ability to work off of mechanical drawings. -High School Diploma or equivalent. -1-3 years prior experience. 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.
    $32k-38k yearly est. 6d ago
  • Senior Quality Engineer- Space

    Lumicity

    Quality Technician Job 44 miles from Manteca

    We're at the forefront of space exploration and satellite technology, designing cutting-edge electronics that push the boundaries of what's possible in space. Our team of innovators is passionate about solving the toughest challenges in space and advancing humanity's presence in the final frontier. We're looking for a Senior Quality Engineer to help us maintain and enhance the quality of our products, ensuring they meet the rigorous demands of space missions. Role Overview: As a Senior Quality Engineer, you will play a critical role in the development, testing, and delivery of high-performance electronics that must withstand the extreme environments of space. You'll be responsible for leading quality assurance efforts across multiple projects, driving process improvements, and ensuring our products meet the highest standards of reliability, safety, and compliance. Key Responsibilities: Lead quality assurance and control activities across all phases of product development, from design to manufacturing and testing. Collaborate with engineering, manufacturing, and design teams to identify and resolve quality issues. Develop, implement, and maintain quality management systems (QMS) and processes in compliance with aerospace industry standards (e.g., AS9100, ISO 9001). Conduct root cause analysis and implement corrective actions for any non-conformance or defects. Perform rigorous testing and validation of electronic components to ensure performance in harsh space environments. Manage product qualification processes, including environmental and stress testing, reliability testing, and qualification to space-specific standards (e.g., MIL-STD, NASA standards). Review and approve supplier quality documentation, and ensure supplier parts meet stringent specifications. Provide mentorship and leadership to junior quality engineers, fostering a culture of continuous improvement and excellence in quality. Stay up to date with industry trends, regulations, and best practices in aerospace and space electronics quality assurance. Qualifications: Bachelor's degree in Electrical Engineering, Aerospace Engineering, or a related field (Master's degree preferred). Minimum of 7 years of experience in quality engineering, with at least 3 years in the aerospace or space electronics industry. Deep knowledge of aerospace quality standards (e.g., AS9100, ISO 9001) and quality control methodologies (e.g., Six Sigma, Lean). Strong experience with space-specific testing methods, such as thermal vacuum, vibration, and radiation testing. Familiarity with electronic design, PCB manufacturing, and testing techniques for high-reliability components. Experience working with cross-functional teams to solve complex technical problems. Proven track record of leading quality initiatives and process improvements. Exceptional analytical skills, with the ability to troubleshoot complex issues and drive root cause resolution. Excellent written and verbal communication skills, with the ability to present complex technical information clearly. What We Offer: Competitive salary and benefits package. Opportunity to work on groundbreaking space technologies that make a real impact. A collaborative, innovative, and supportive work environment. Professional development opportunities and career growth. Flexible working arrangements to support work-life balance.
    $112k-152k yearly est. 6d ago
  • Quality Inspector - Parachute Rigger

    U.S. Army 4.5company rating

    Quality Technician Job 41 miles from Manteca

    92R Parachute Rigger Seeking detailed oriented individuals to perform everyday tasks that save lives. You will build inspections skills as you become an expert in inspecting, packing, and repairing parachutes. Similar Jobs: Occupational Safety Inspector and Quality Control Inspector
    $38k-49k yearly est. 7d ago

Learn More About Quality Technician Jobs

How much does a Quality Technician earn in Manteca, CA?

The average quality technician in Manteca, CA earns between $33,000 and $77,000 annually. This compares to the national average quality technician range of $27,000 to $50,000.

Average Quality Technician Salary In Manteca, CA

$51,000
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