Quality control inspector jobs in Temecula, CA - 297 jobs

Career-defining. Life-changing. At iRhythm, you'll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what's possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career About This Role: The 2nd Shift Quality Control (QC) Inspector is responsible for supporting manufacturing operations during second shift by performing inspection, documentation review, and batch release readiness activities for finished goods and sub-assemblies. This role focuses on reviewing batch records, travelers, and routers, ensuring Good Documentation Practices (GDP) compliance, identifying quality issues, and initiating nonconformances (NCs) when required. The QC Inspector also provides Receiving Inspection (RI) support as needed to ensure material flow continuity and compliance with inspection requirements. Why This Role Is Critical * Provides real-time quality oversight on second shift, ensuring batch records, travelers, and GDP compliance are verified at the time of execution rather than retrospectively. * Enables timely identification and containment of nonconformances, reducing quality escapes, rework, and compliance risk. * Supports on-time release readiness and uninterrupted manufacturing flow, preventing inspection and documentation backlogs into first shift. * Strengthens audit readiness and cross-shift continuity, ensuring clear handoff and sustained control of quality issues across shifts. What You WIll Be Doing Batch Record, Traveler & Router Review * Perform detailed review of batch records and travelers for finished goods and sub-assemblies to ensure completeness, accuracy, and compliance with approved procedures. * Verify that all required manufacturing steps, inspections, testing reports, in-process checks, and approvals are properly completed and documented. * Ensure material traceability, including material lots, subassemblies, equipment identification (when applicable), and inspection status. * Access and reference the electronic Quality Management System (eQMS) to ensure the current, approved revisions of drawings, specifications, procedures, and work instructions are used during inspection and batch record review activities. * Verify that batch records, travelers, and inspection activities are executed against the correct released document revisions, and escalate discrepancies when outdated or incorrect documents are identified * Identify documentation errors, omissions, or discrepancies and ensure timely correction in accordance with GDP requirements. Finished Goods & Sub-Assembly Inspection * Perform in-process, final, or verification inspections of finished goods and sub-assemblies per approved inspection plans and work instructions. * Ensure inspection results are accurately recorded and aligned with acceptance criteria. * Support timely review and release readiness of manufacturing lots to maintain production flow. Nonconformance Identification & Escalation * Identify, document, and initiate Nonconformance (NC) records when inspection results, documentation, or material conditions do not meet requirements. * Ensure nonconforming material is properly identified, labeled, and segregated to prevent unintended use. * Escalate quality issues to Quality Control leadership and Manufacturing supervision as required. Good Documentation Practices (GDP) Compliance * Enforce GDP standards across all reviewed records, including batch records, travelers, routers, and inspection forms. * Ensure corrections, clarifications, and late entries (when applicable) are performed per approved GDP procedures. * Support identification of recurring documentation issues and participate in corrective actions or retraining as needed. Receiving Inspection (RI) Support * Perform Receiving Inspection (RI) activities when required, following approved sampling plans, inspection criteria, and procedures. * Verify material identification, lot traceability, and acceptance status. * Accurately document RI results and communicate material status to Manufacturing and Quality teams. Compliance & Audit Readiness * Perform all activities in compliance with ISO 13485, and internal QMS SOPs, DOP's and work instructions. * Maintain inspection areas and records in a state of audit readiness. * Support internal audits and regulatory inspections by providing accurate records and inspection evidence as requested. Cross-Shift & Cross-Functional Communication * Communicate inspection results, documentation issues, and open quality concerns clearly during shift handoffs. * Collaborate with Manufacturing, Quality Engineering, Receiving, and first-shift QC personnel to ensure continuity of quality controls. What We Want to See * High School Diploma or GED required; Associate's or Bachelor's Degree in a technical or life sciences field is preferred. * Minimum of 2-5 years of experience in a medical device manufacturing, pharma, aerospace or regulated manufacturing environment, preferably in Quality Control or Inspection. * Experience navigating an electronic Quality Management System (eQMS) to review and reference released drawings, specifications, SOPs, and work instructions * Working knowledge of Good Documentation Practices (GDP) and controlled document execution. * Experience reviewing batch records, travelers, routers, and inspection records. * Ability to identify quality issues and initiate nonconformance records in accordance with established procedures. * Strong attention to detail with a focus on accuracy, compliance, and data integrity. * Ability to work independently on second shift with minimal supervision. * Effective verbal and written communication skills. * Ability to manage multiple tasks and prioritize work to support production needs. Ways to Stand Out * Experience performing Receiving Inspection (RI) or FAI activities. * Familiarity with sampling plans, inspection plans, and acceptance criteria. * Demonstrated experience reviewing engineering drawings, including GD&T, to identify critical-to-quality (CTQ) characteristics, specification notes, and applicable inspection requirements, and applying them during inspection and batch record review * Experience using enterprise resource planning (ERP) systems (e.g., QAD, SAP) to support manufacturing execution, batch review, material status, and traceability is a plus Location: Orange County Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location. Estimated Pay Range $21.15 - $26.44 As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws. iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at ********************* About iRhythm Technologies iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm's vision is to deliver better data, better insights, and better health for all. Make iRhythm your path forward. Zio, the heart monitor that changed the game. There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a @irhythmtech.com email address. Please check any communications to be sure they come directly from @irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact *********************. Written offers of employment will be extended in a formal offer letter from an @irhythmtech.com email address ONLY. For more information, see *********************************************************************************** and *****************************************

For five decades, HPI Architecture has shaped environments that do more than function, they inspire, support, and enrich lives across generations. Our work bridges people and place, creating meaningful spaces rooted in purpose and designed with intention. Our brand promise reflects who we are: With intention, we approach each project with curiosity, creativity, collaboration, and technical finesse. Fully engaging in the process, we design places that reflect the vision and values of our clients and the people they serve. At HPI, you'll grow through continuing education, mentorship, and professional development, with opportunities to expand your skills and elevate your craft. We also offer a flexible schedule and hybrid work options to support balance, collaboration, creativity, and well‑being. As we embark on the next 50 years, we're seeking an Architectural Specifier / Quality Controller to help uphold the technical excellence, coordination, and material integrity that define our legacy of thoughtful, high-performing design. How You Will Make an Impact: Produce coordinated Project Manuals using CSI formats, developing specifications from Schematic Design through Construction Administration. Conduct thorough product research, evaluate alternatives, maintain vendor relationships, and support teams with material and product selection. Collaborate with Technical Directors and Project Architects to develop and maintain office-wide specification standards. Review drawings, Revit models, and Keynote lists to ensure alignment with specifications, providing clear technical guidance across all project phases. Perform Quality Control reviews at key milestones-evaluating code compliance, accessibility, constructability, life safety, and coordination across disciplines. Use Revit and Bluebeam Sessions to review documentation and confirm comment resolution. Support bidding and construction administration by assisting with RFIs, submittals, and product substitutions. Participate in project and consultant coordination meetings, staying current with building codes, DSA requirements, and industry best practices. Manage multiple active projects simultaneously, maintaining accuracy, consistency, and deadlines. To Be Successful in This Role, You Must: Demonstrate expert knowledge of building systems, construction techniques, materials, and codes. Communicate technical information clearly and collaborate effectively across teams. Be highly organized, detail-oriented, and able to manage multiple deadlines. Bring strong problem-solving abilities and provide thoughtful, solutions-oriented feedback. Work confidently in a fast-paced, multi-project environment. Show initiative in improving standards, documentation practices, and material research. Leverage Revit and Bluebeam to support accurate, coordinated design review processes. To Qualify, You Must Have: A minimum of 10 years of relevant architectural experience, including at least 5 years of specification writing. Experience preparing architectural specifications using AIA MasterSpec. Strong understanding of building codes, materials, construction techniques, and sustainability requirements. Proficiency in Microsoft Office, Bluebeam Revu, and specification editing software. CSI certification preferred. LEED Accreditation and/or CASp certification a plus. Knowledge of DSA requirements preferred. Knowledge of Revit and Revit add-ins for specifications and keynotes a plus. A professional degree in Architecture is a plus. Excellent communication and collaboration skills. Pay, Perks & Benefits Flexible Schedule and Hybrid Work Opportunities Vacation and Sick time Medical, Dental, and Vision Insurance with additional Supplemental Insurance options 401(k) Ongoing professional development with access to continuing education and meaningful mentorship Licensure Assistance Salary Range: $105,000.00 To $135,000.00 Annually Our Core Values CLIENT CENTERED: We're all in-listening first, collaborating closely, anticipating needs, and actively engaging with our project partners and one another. DESIGN EXCELLENCE: We dig deep to uncover the unique needs of our clients-shaping purposeful, inspiring, and enduring spaces for solutions rooted in people. PROFESSIONAL INTEGRITY: We own our role and take pride in our work, delivering an exceptional experience every step of the way that excites. Ready to help shape the next 50 years of meaningful design? We'd love to meet you! Recruiters, please do not contact this job poster.

Quality Inspector 1st Shift - Riverside, CA Portables M-F 6:30AM-3PM $20.12-$23.74Hr LUXFER GAS CYLINDERS is the world's largest manufacturer of high-pressure composite cylinders. We have a proven record for dependability and safety. American Made products that save the lives of firefighters and first responders!! JOB DESCRIPTION: You will perform inline quality inspections, checks, and tests during the manufacturing process. Records defects on a daily basis and may make recommendations for improving processes. As a Quality Inspector, you will work closely with Production to identify nonconforming materials on the shop floor. ACTIVITIES: The main activities of the position include but are not limited to the following: * Responsible for inspecting materials for quality and defects. * Inspects cylinders internally, externally, and dimensionally to ensure they meet all internal and external customer requirements. * Perform in-process inspection and final inspection. * Identify non-conforming material and notify the Quality Lead or Team Leader to generate non-conforming material reports. * Generate rework tags and send nonconforming material to various areas for rework. * Give feedback from personal experiences on the shop floor to help improve Production/Quality processes and possibly assist in implementing and testing out these new processes. QUALIFICATION/REQUIREMENTS: * Able to lift product and stand for extended periods of time. * Ability to read Pi-Tape, Calipers, Depth Gauge, and a weight scale. * Requires a high school diploma or its equivalent and 2 years of related experience. * Familiar with standard concepts, practices, and procedures within the quality function. * Relies on experience and judgment to plan and accomplish goals. * Demonstrated ability to troubleshoot and problem solve. * At least 18 years old * Able to pass a Drug Test * The acceptable outcome of a Background Check We are committed to a safe, drug-free work environment and pre-employment drug screening, physical and background checks are required prior to starting. Candidates must be authorized to work in the US. Luxfer Cylinders is an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities. Women, minorities and veterans are encouraged to apply. NOTICE FOR CALIFORNIA RESIDENTS Pursuant to the California Privacy Rights Act, if you are a California resident, you have the right to know the categories of personal information we collect and how it's used. Please visit the site below to access our California Privacy Rights Act Policy for candidates and employees. ******************************************************************************************************************************************

From Engine Bay to Payload, we protect vital structures and systems. Hera Technologies is a premier contract manufacturer specializing in high-precision metallic and non-metallic solutions for the Aerospace, Defense, Space, and Commercial Airline sectors. Our commitment to quality, innovation, and customer satisfaction has positioned us as an industry leader in the design, manufacturing and maintenance of thermal support systems. Our team is driven by excellence, integrity, and a passion for advancing aerospace technology. Take the next step in your career with a company committed to excellence, where your contributions are recognized, and your potential is realized. Take the next step in your career with a company committed to excellence, where your contributions are recognized, and your potential is realized. Role OverviewThis is a full-time, on-site role for a Quality Control Inspector located in Ontario, CA. The Quality Control Inspector will be responsible for conducting inspections, ensuring quality control and quality assurance, and managing quality-related processes. The inspector will perform regular quality checks, document findings, analyze quality data, and maintain records. The role also involves collaborating with other team members to identify and address any quality issues and implementing corrective actions to ensure products meet the company's standards.Key Responsibilities Conduct in-process and final inspections of products to ensure conformance to standards. Perform regular quality checks, document findings, and analyze quality data. Maintain accurate and detailed records of inspections and test results. Collaborate with production teams to identify and address quality issues. Assist in implementing corrective actions to ensure products meet company standards. Ensure all processes and products adhere to industry standards and regulations. Required Qualifications Proven experience in Quality Control, Quality Assurance, and Inspection. Experience with Quality Management systems and processes. Strong communication skills. Excellent attention to detail and problem-solving abilities. Ability to work independently and as part of a team. Knowledge of industry standards and regulations. Associate degree or equivalent relevant experience. Preferred Qualifications Bachelor's Degree is preferred. Additional certifications in quality control or related fields are a plus. Previous experience in a manufacturing or fabrication environment is beneficial. Additional Requirements: Willingness to work long hours and weekends when needed to meet critical deadlines Willingness to travel to customers' locations or other Hera sites as needed Ability to use a computer and most common software programs to complete assignments Ability to communicate with individuals and groups in person, by phone and online Your actual level and base salary will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, education, and experience. The base salary is just one part of your total compensation package at Hera. You will also have access to a comprehensive set of benefits like: Company paid employee medical, dental and vision insurance Retirement plan participation (eligibility required) Paid Sick LeavePaid VacationPaid holidays Discretionary bonuses Physical Requirements / Work Environments· Ability to work in office, lab, and manufacturing environments with occasional exposure to noise, dust, and temperature variations· Must be able to lift and carry up to 35 lbs and perform tasks involving standing, walking, bending, and manual assembly· Visual acuity required for reading technical drawings and digital media· Valid US driver's license and ability to operate motor vehicles The above statements are intended to describe the general nature and level of work performed. They are not intended to be an exhaustive list of all responsibilities, duties, or skills required. Management may modify or assign additional duties as needed. EXPORT CONTROL REQUIREMENTS:To conform to US Government export regulations, the applicant must be a (i) US Citizen, (ii) lawful permanent resident of the U.S. (aka green card holder), (iii) protected individual as defined by U.S.C. 1324b(a)(3), or (iv) eligible to obtain the required authorizations from the U.S. Department of State. Hera Technologies is an Equal Opportunity Employer, employment with Hera Technologies is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Job Description This position is responsible for performing in-process, component and finished goods visual and dimensional inspections using SPC/AQL sampling plans to support production, incoming receiving inspection and Quality investigations as needed. These inspections utilize industry standard metrology and gaging methods to identify defects and ensure product meets customer requirements. This position works on the production floor sampling, performing visual inspections and assessing quality of the parts and process. Attention to detail and the ability to work with minimal amount of supervision and understanding of quality inspection tools and equipment is required. Essential Job Functions and Responsibilities: Perform dimensional and visual In-process and finished good inspection on parts/boxes per approved control plans, test methods and customer drawings. Quality / SPC evaluation when required per site documentation. Communicate with Machine Technicians, Operators and Production Supervisors inspections/SPC results to operation when defects are detected to ensure process adjustments are made and in an effort to run a consistent quality product. Review daily NCR reports, SPC charts and quality system documentation. Enforce and maintain our Quality System and provide suggestions to maintain our continuous improvement system. Visually and dimensionally evaluate product and packaging in accordance with established acceptance criteria and standards. Follow all Safety rules and guidelines. Report any unsafe condition or practice. Maintain a clean work area throughout the shift. Evaluate product documentation for adequacy and completeness. Visually and dimensionally evaluate product and packaging in accordance with established acceptance criteria and standards. Measure process performance against established acceptance criteria and standards. Record real time data and prepare formal reports. Other assignments as may be given by the Quality Engineer or Managers. Support maintenance and calibration requirements for Quality Lab and production floor Place non-conforming product on hold and create non-conforming records and assist with Quality inspections of rework product as needed. Partner with Quality Control department for the management of product retains. Update Quality Inspection requirements Assist in the creation, closure review and verification of completion of batch records and release products and issuance of certificates of compliance to ensure product produced meet the customer and regulatory requirements Assist with New Product validation as required. Participate in Gage Repeatability and Reproducibility (GR&R), Geometric Dimensioning and Tolerancing (GD&T or GD and T) Intermedium studies and product/process validations Review and release product for shipping though issuance of COC ensuring all Customer requested documents are provided at the time of shipment Maintain cleanliness of QC lab, implement and sustain 6S, Quality boards and speak to status of site Quality metrics Able to generate and reconcile Labels (as needed) Perform Environmental monitoring activities according to site procedures. Train Quality personal on environmental monitoring activities and clean room requirements. Other assignments as may be given by the Quality Supervisor or Plant leadership team. Core Competencies: Statistical Process Control Knowledge Cosmetic, visual and dimensional Inspection Housekeeping General Safety Communication & Teamwork Skills Computer literate. Good verbal and written communication skills. Ability to perform standard measurement and test equipment. Attendance-dependability Time Management IQMS Knowledge Inspection Skills Organizational Skills Basic math skills Metrology Blueprint Reading Data Entry Skills Knowledge, Skills, and Abilities Read and write in the English language. Must be able to perform basic math such as addition, subtraction, multiplication, division, fractions, and decimals. Ability to read and interpret basic engineering drawings and product specifications. Proficiency with utilizing ANSI Sampling Plans Proficient in utilizing hand measurement tools (Caliper, Micrometer, Ruler, Gage Blocks, etc.) Experience with PCDMIS and Measuremind 3D automated inspection software usage (CMM, OGP, Smart scope, etc.) and programming a plus Knowledge of Medical device standards and Regulations (ISO 13485) Ability to read and decipher blueprints Knowledge of GD&T Experience with handling non-conforming material Experience with device history record creation and review Knowledge of ERP and quality system elements Proficiency in using Microsoft Excel, Access Database and Word Experience in supporting process validation activities including testing and Gage R&R Knowledge of sample plans creation is a plus Understanding of risk management is a plus Education and/or Experience: High School Diploma or GED. Minimum 6 months factory related experience in a regulated industry. Minimum of one year experience in visual and dimensional evaluation of molded products; or minimum three years experience in plastic injection molding and assembly processes Experience with calipers and micrometers is required; Other inspection equipment such as indicators, height gage, & pin gauges are a plus. Should have prior experience in a manufacturing environment to understand normal safety requirements. Certified Quality Inspector or Technician a plus

Quality Control Inspector II is a hands-on role, whose primary responsibility consists of the inspection and measurement of products to ensure that they are in spec at the point of production. POSITION DUTIES/RESPONSIBILITES Able to read different measuring gages, understanding of gage calibration, receiving inspection of components, validate process and test reports, In-process inspection, generate Nonconformance reports, read travelers, work with industry and customer specifications, understands QMS function, review P.O. for shipping orders to ensure correct delivery address, prepare paperwork for shipping of product, Customer source inspection, verification of resin mix, understanding of composite inspection, train new inspectors, develop performance metrics, complete corrective action reports, work with supplier quality issues, perform internal audits. Qualifications 5 years minimum experience in Mechanical Inspection NDT Ultrasonic Testing experience, Level II preferred Experience with AS 9100 and ISO 9001 ROMER Arm experience, PCDMIS, Verisurf, Polyworks Use calipers, micrometers, height gages and scales Blueprint reading GD&T, computer proficient Generate FAIR per AS9102Must be able to meet ITAR eligibility Must be eligible to obtain and maintain a U.S. Government security clearance required for assigned programs PHYSICAL DEMANDS N (Not Applicable) Activity is not applicable to this position.O (Occasionally) Position requires activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires activity more than 66% of the time (5.5+ hrs/day) Physical Demands Lift/Carry 10 lbs or less F 11-20 lbs F 21-50 lbs F 51-100 lbs O Over 100 lbs N Push/Pull 12 lbs or less F 13-25 lbs F 26-40 lbs F 41-100 lbs O Other Physical Requirements Must be able to lift and carry items weighing up to thirty-five (35) pounds on a repetitive basis. Must be able to stand, walk, bend, squat, climb, kneel, twist, and work at heights on an intermittent basis for up to twelve (12) hours. Requires hand manipulation including simple grasping, pushing, and pulling materials. Must be able to reach and work above and below the shoulder level. Must be able to work with and around forklifts and hazardous machinery. Must be able to remain in a stationary position such as working at a desk on a computer for prolonged periods of time. Visual acuity skill to detect any flaws in the parts being inspected. Ability to wear Personal Protective Equipment (PPE) - Required Safety Glasses

Full-time Description Shift: 2:30pm - 11:00pm Scope: Inspect and evaluate final products to ensure compliance to customer requirements prior to delivery. Essential Job Function: Perform Final Inspection on finished product to ensure compliance to customer requirements. Read customer drawings Perform measurements with measurement tools such as calipers, micrometers, and pin gages. Perform rework as appropriate, which may include mask touch-up, material removal with an x-acto knife, burnishing, soldering irons, final finish brush plating, sanding Verify acceptability of rework after completion Identify and mark non-conforming product to ensure it is not delivered Prepare standard and AS9102 First Article Reports as needed Verify certifications and reports are complete and accurate and can be used for final acceptance and certification of product Complete Deliverables for Customers and ensure they are complete and accurate Complete department logs and record yield data as required Perform preventative maintenance as defined by department maintenance schedule Support other work areas or departments as required by production or management. Ability to work overtime as requested Keep work area clean and organized Requirements Essential Qualifications, Education and Experience: High school diploma or equivalent One year of PCB manufacturing experience Knowledge of IPC-6012, or IPC-6013 Knowledge of IPC-600 Strong work ethic Ability to work effectively in a team environment Physical Requirements: Prolonged periods sitting and performing visual and manual tasks. Fine motor skills Ability to use microscopes for long periods of time performing job duties ITAR Compliance Requirement: This position requires access to controlled technical data and/or participation in activities subject to the International Traffic in Arms Regulations (ITAR). As such, all applicants must be U.S. persons, as defined by ITAR (U.S. citizens, U.S. lawful permanent residents, or individuals with refugee/asylee status). Candidates who do not meet ITAR eligibility requirements will not be considered for this position. AdvancedPCB is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, status as a protected veteran, marital status, genetic information, medical condition, or any other characteristic protected by law (EEOC). Compensation: Exact compensation may vary based on skills, experience, and location. About AdvancedPCB AdvancedPCB is a leading manufacturer of high-reliability printed circuit boards. The company features 6 total manufacturing sites: Santa Clara, our headquarters in the heart of the Silicon Valley; 2 in Southern California, 1 in Maple Grove, Minnesota, Aurora, Colorado and Chandler Arizona. Currently, the company is viewed as over $100 Million; 180,000 sq. ft. of manufacturing space with over 480 employees, making AdvancedPCB one of the largest privately held printed circuit board manufacturers in North America. Visit us! ********************************** Salary Description $18.00- $24.00

Job Title: Quality Control Inspector (Aerospace Job Shop) Department: Quality Assurance Reports To: Quality Manager Employment Type: Full-Time We are seeking an experienced Quality Control Inspector with a minimum of 5+ years in aerospace manufacturing to join our fast-paced job shop in Corona, CA. This role is responsible for performing in-process, first article, and final inspections using advanced measurement tools, including portable CMM equipment such as a Romer Arm. The ideal candidate must be highly proficient in GD&T, blueprint interpretation, and AS9100 requirements. Key Responsibilities Inspection & Measurement Perform first article, in-process, and final inspections on aerospace components in accordance with customer, engineering, and industry standards. Operate and program Romer Arm or similar portable CMM equipment to perform high-accuracy dimensional inspections. Use precision measurement tools including calipers, micrometers, height gauges, surface plates, bore gauges, and optical comparators. Interpret and apply Geometric Dimensioning & Tolerancing (GD&T) to inspect complex features and assemblies. Document inspection results and complete required forms, reports, and digital records. Quality Assurance Ensure products meet all customer specifications, engineering drawings, and AS9100/ISO quality standards. Identify, document, and report nonconformances; assist in root cause analysis and corrective actions. Support the creation and maintenance of First Article Inspection Reports (FAIRs) to AS9102 standards. Verify certifications, material traceability, and documentation packages for final release. Manufacturing Support Work closely with machinists, engineers, and production staff to resolve quality issues on the shop floor. Provide feedback on manufacturability, drawing interpretation, and potential process improvements. Assist in developing inspection methods and fixturing when required. Qualifications Experience 5+ years of Quality Control/Inspection experience in an aerospace or precision machining environment. Strong, hands-on experience with Romer Arm / portable CMM inspection tools. Proven expertise in GD&T (ASME Y14.5) and interpreting complex aerospace drawings. Education High school diploma or GED required; technical training or certifications in inspection, CMM, or aerospace manufacturing preferred. Technical Skills Proficiency with: Portable CMM systems (Romer, Faro, or equivalent) GD&T application and interpretation Reading complex blueprints and 3D models Standard inspection equipment (manual and digital) AS9100 & AS9102 First Article requirements Experience with ERP/MRP systems and digital inspection software a plus. KPG123

Job Title: Quality Control Inspector Skills Required: In the Quality Inspector role, you will be responsible for inspection and quality services to ensure company products and processes meet customer, company, and other specifications. This role supports company initiatives, provides training and assists the Quality Control Manager. Essential Responsibilities: Comply with all quality, safety, and work rules and regulations. Evaluate problems and make initial recommendations for possible corrective action to supervisor. Participate in the construction and/or revision of SOPs for the inspection function. Provide support to production team when required. Visually and physically inspects materials, components, subassemblies, assemblies, tools, and final product configuration using blueprints, sketches, engineering drawings, and orders, and other applicable sources to observe, measure, record conformity to customer, regulatory, and company specifications. Records compliance with quality standards to verify that company products and processes meet customer, company, and other specifications. Solves inspection problems; methods-procedures, plans, and details. Audits products and processes to verify system. Maintains necessary inspection logs and writes inspection reports. Communicate quality problems and work with engineering and leads to support, investigate and resolve the quality issues. Perform all other duties as assigned. Minimum Requirements: Ability to manage multiple tasks, set priorities, identify, address problems and meet deadlines. Self-motivated with ability to work independently in a fast-paced environment with changing priorities. Computer skills to include Microsoft programs. Must be able to use computer programs to keep track of administrative tasks such as report writing, analysis of work orders, evaluations, etc. English skills must be proficient to understand, read, write and speak English. Ability to work overtime and weekends as required. Must be committed to the success of the entire organization. Physical Requirements: Must be able to stand and walk for prolonged periods of time. Must be able to lift and carry up to 25 lbs. Must be able to push, pull, twist, climb, balance, stoop, kneel, and crawl. Must be able to perform repetitive motions such as reaching and grasping. Must be able to use a ladder or step ladder. Work environment is in a warehouse and temperatures inside vary between hot or cold based on the outside conditions. This is a fast-paced environment with constantly changing priorities. Education/Experience: High School diploma or equivalent preferred. Minimum of 3 years of experience in a similar role or a combination of experience and education will be considered. Familiar with SQF 2000, HACCP, and GMP preferred. Experience in the plastic bottle industry or in a manufacturing environment is preferred.

Responsibilities: Perform visual and dimensional checks various incoming products (sheet metal, PCBAs or CCAs, Printed Boards or PCBs, Conformal Coating, Labels or markings, Cables, Harnesses; COTS items, and etc.) at various stages (Incoming, RMA, In-process, Final, Shipping, etc.) Test and or verify products for a variety of characteristics such as functional performance mechanically or electrically, or chemical properties or composition. Perform First Article Inspection and prepare FAIRs as needed. Record Inspection findings and generate NCMR's, DCRs' and ERRs' as needed. Communicate with the Project Mangers or QA for any possible delays and/or resolutions of any urgent and high priority jobs. Required: Extensive working knowledge of IPC-A-600, J-STD-001 and IPC-A-610, and IPC-A-620. Prior or current IPC training and/or certification is preferred. Ability to read, comprehend and interpret engineering drawings and documentation such as electrical schematic diagrams, mechanical and assembly drawings, BOM, and assembly instructions, and etc. Ability to adjust in fast-paced dynamic operations. Ability to apply concepts of basic algebra and geometry such as decimals, fractions, length, proportions, percentages, area, circumference, and volume. Ability to confer with management or engineering staff to determine quality and reliability standards or applicable requirements. Ability to use mechanical measurement tools such as calipers, micrometers, and electrical measurement tools, etc. Ability to operate computers and able to use computer applications and files such Microsoft Word and Excel, Adobe PDF, Outlook emails, and other databased platforms. Detail oriented, dedicated and self-motivated. Ability to work under minimum supervision. Work well in a team environment. Must have good interpersonal skills.

Insight Global is looking for a Quality Control Inspector for a medical device client in the Irvine, CA area. They will be responsible for in-line inspections, both top assemblies and finished goods. This position is for 2nd shift (3pm-11:30pm, Monday-Friday). The training for the first month or two with be first shift (7am-3:30pm, Monday-Friday). They will then learn and be a part of receiving inspections once comfortable with training. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements 3 years of QC experience specifically in a production line (In-Line) Medical Device experience strong computer skills Strong knowledge of NCR (non-conformit reports) Detail-oriented Receiving inspection experience ERP experience

The Quality Control Inspector is responsible for verifying that Solar PV, BESS, and EV projects are installed in compliance with design drawings, codes, standards, and client requirements. This role ensures quality assurance through inspection, documentation, and enforcement of corrective actions.

Job DescriptionQuality Control InspectorAre you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our reputable biotech diagnostic company. Location: CarlsbadPay Rate: $18 - $19.80/hr, contract Both 1st shift and 2nd shift available, Monday-Friday and weekends as needed Key Responsibilities: Perform routine and special inspections for visual, dimension, and functional assessments, ensuring adherence to inspection instructions. Document and report inspection findings, monitoring corrective actions for any identified issues. Execute product identification and traceability activities as required. Review, approve, and maintain Device History Records for all manufacturing functions, in compliance with relevant standards and regulations. Apply in-depth knowledge of QSRs/ISO and regulatory guidelines to daily tasks, ensuring quality standards are upheld. Monitor and comply with customer specifications and company quality assurance policies. Ensure proper calibration and maintenance of inspection equipment. Essential Functions: Conduct and document hourly inspections. Perform and document line clearance procedures. Carry out First Articles and Retention Samples, documenting and filing accordingly. Review, approve, and file documents for completeness and compliance. Work Environment:The work environment encompasses warehouse, laboratory, and manufacturing settings, where handling viral and bacterial hazards, potentially hazardous chemicals, and infectious bodily fluids and samples may occur. Flexible work hours may be required to meet project deadlines. Education, Skills & Experience: Minimum 6 months of Quality Control inspection experience required. Experience with Good Manufacturing Practice (GMP) Experience in a medical device high-volume manufacturing environment is strongly desired. Ability to read, interpret, and follow detailed procedures, instructions, and drawings. Solid understanding of QSRs/ISO standards. Demonstrated team-oriented interaction skills and professional behavior. Proficiency in word processing, data entry, and spreadsheet navigation. Familiarity with basic quality terms, definitions, and concepts. Understanding of traceability (product, material, and calibration). Basic math skills for determining appropriate sample sizes for inspection based on lot sizes. Problem-solving skills to identify processes and standards in need of improvement and initiate appropriate action. If you are driven by a commitment to excellence and have a passion for quality control in the biotech industry, we encourage you to apply. Join our dedicated team and make a significant impact on healthcare by maintaining the highest quality standards in our biotech diagnostic products.

The Quality Control Inspector is responsible for performing inbound inspections, in\-house testing, and quality investigations to ensure all raw materials, finished goods, components, and accessories meet internal specifications and regulatory standards. This role works closely with the Quality Lead and cross\-functional teams to support continuous quality improvement. Key Responsibilities Perform in\-house investigations to ensure adherence to internal quality standards for raw chemicals, finished goods, components, machines, and accessories Maintain internal finished goods and labeling standards Partner with the Quality Lead to maintain non\-conformance logs and provide quality metrics supporting KPIs Execute and document special projects, including new component testing and planned E&O exercises Monitor on\-hand waste and coordinate routine waste pickups Conduct product assessments, including: Physical: color, odor, appearance, etc. Analytical: torque, specific gravity, pH, viscosity, etc. Operate and be cross\-trained on QC lab equipment (pH testing, viscosity testing, specific gravity, and related tools) Analyze product characteristics against specifications and determine disposition (pass\/fail), including review of Certificates of Analysis (COAs) Adhere to Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) Escalate quality issues in a timely manner using clear and appropriate quality terminology Assist with audits and special testing requests under the guidance of the Quality Manager Support production, warehouse, and quality teams as needed Job Requirements Strong written and verbal communication skills in English; Spanish proficiency is a plus High commitment to safety, especially when working with laboratory equipment Basic math skills with the ability to interpret analytical data Ability to climb ladders, remain on feet for up to a 10\-hour shift, and lift up to 50 lbs Ability to collect samples from containers up to 72” tall Strong ability to prioritize and adapt to changing production needs Exceptional attention to detail ASQ Certified Quality Inspector (CQI) preferred 30 \/ 60 \/ 90 Day Expectations First 30 Days Fully understand inbound inspection processes and clearly explain responsibilities, procedures, and value to the organization Build relationships with key and cross\-functional teams and understand role alignment Manage inbound receipt inspection tracking and provide weekly summaries of rejected materials By 60 Days Assist with retains and standards management and independently support investigations Support the Quality Lead with non\-conformance investigations (NCRs), including timely escalation and closure By 90 Days Conduct trend analysis on rejected inbound materials Provide high\-level summaries outlining impacted items, common issues, quantities, and vendor data Pay Rate: $19\/hour Schedule: 6:00 AM - 2:30 PM (overtime and weekend availability required as needed) "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"653983288","FontFamily":"PuviRegular","job OtherDetails":[{"field Label":"Job Opening ID","uitype":111,"value":"ZR_2506_JOB"},{"field Label":"Industry","uitype":2,"value":"Manufacturing"},{"field Label":"Salary","uitype":1,"value":"19"},{"field Label":"Salary Type","uitype":2,"value":"Hourly"},{"field Label":"City","uitype":1,"value":"Fontana"},{"field Label":"State\/Province","uitype":1,"value":"California"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"92335"}],"header Name":"QC Inspector","widget Id":"4**********0072311","awli IntegId":"urn:li:organization:3525447","is JobBoard":"false","user Id":"4**********0184003","attach Arr":[],"awli ApiKey":"861ql0p5wym4v2","custom Template":"3","awli HashKey":"66ba2a8eeb5a681ba7da00d31a032d7817c4e5dab8f6c880d8eafd16e2274f43b413d096a**********10b0669a46e69610344ec56ef093aa867f744e099feff","is CandidateLoginEnabled":false,"job Id":"4**********8088056","FontSize":"15","google IndexUrl":"https:\/\/greathirehr.zohorecruit.com\/recruit\/ViewJob.na?digest=Qx8B8qu1HVi@**************************@VJP8\-&embedsource=Google","location":"Fontana","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"5a0s1eed**********48682b45b77ac5327c6"}

Job DescriptionDescription: Chemical Guys is more than a brand, it's a lifestyle with a worldwide following. Driven by adventure, a passion for shine, and a love for the road ahead, we welcome any and all who share this passion to become part of our family. When we started, we decided to wipe the slate clean and start off fresh with the simple idea to make the best quality chemicals manufactured right here in California to the highest quality standard. Over the years, we have grown into so much more: a huge library of detailing knowledge, a benchmark in the industry, group of friends with one common passion. Today, Chemical Guys has become a true omnichannel leader in automotive appearance industry with a massive social media following and product distribution around the World. But we know this is still just the beginning as we want to win in the long run, drive innovation, and refine the industry while having fun and smiling along with you. So, grab a wash mitt, some soap, put a smile on your face, and don't look back… it's going to be an unforgettable ride! Summary of Position The Quality Inspector is responsible for ensuring all products meet & exceed quality expectations from receiving of inbounds to finished good output in production. As a Quality Inspector, you will oversee all Quality Control processes performed in-house and work closely with the Quality Control Lead when performing investigations for root cause analysis & CAPA implementation in the spirit of continuous improvement. Job Responsibilities Perform in-house investigations to ensure adherence to internal standards across the following categories: Raw chemicals, finished goods, components, machines, accessories, etc. Maintain in-house internal finished good standards & label standards. Work alongside the Quality Lead in maintaining a non-conformance log & providing quality metrics to support KPIs. Execute & document unique projects from the testing of new components to the execution of planned E&O exercises. Monitor on-hand waste to schedule & support routine pickups. Perform product assessments, including but not limited to - -Physical: Color, Odor, Appearance, etc.-Analytical: Torque, Specific gravity, pH, Viscosity, etc. Be cross trained in operating QC lab equipment for performing in house testing, including but not limited to: pH testing, viscosity testing, specific gravity. Analyze product characteristics against established specifications/standards to determine disposition (i.e. pass/fail). Includes evaluation of several Certificates of Analysis (COAs) Adhere to basic principles of GLP & cGMP to expand these practices department wide. Perform timely escalations with strong communication skills using appropriate terminology. Under the guidance of the Quality Manager, facilitate & assist in unique audit requests & testing when required. Assist production, warehouse, and quality personnel as required. Location: 13481 Valley Blvd. Fontana, CA 92335 Compensation: $19/hr Job Type: Full Time with either temp to hire(benefits provided when you become perm. employee) or permanent hire from the start 30/60/90 Deliverables 30 Day Fully comprehend the concept of inbound inspections and be capable of verbally speaking to all processes the position is responsible for with clear explanations of how to perform & the value it brings to the organization. Build relationships with key team members & cross functional teams and provide a brief explanation of how their roles intertwine with the responsibilities of the QC Inspector. Manage an inbound receipt and approval/rejection tracker for all items inspected and provide weekly summaries of rejected materials. 60 Day Assist in Retains & Standards management and be capable of fully owning the process to support unique investigations. Support the Quality Lead in conducting investigations & take ownership of projects related to Non-Conformances (NCRs) in pursuit of timely escalations and closures. 90 Day Begin conducting trend analysis for rejected materials at inbound and provide a high-level summary including, but not limited to: items impacted, shared issue(s), quantities impacted, vendor information, etc Requirements: Job Requirements Strong written & verbal communication skills in English. Proficiency in Spanish is a plus. High prioritization of safety and caution when utilizing sensitive laboratory equipment. Knowledge of basic mathematics to be able to understand & analytical data. Physically be able to climb ladders, stay on feet for a full 10hr shift and lift 50 lbs. Physically be able to obtain samples from containers up to 72” tall. Ability to prioritize & pivot daily activities driven by production urgency. Relentless attention to detail. American Society for Quality (ASQ) Certified Quality Inspector (CQI) preferred.

Join our dynamic team in San Diego, CA, a hub for innovation and biotechnology, where you can leverage your skills in a thriving environment. We are seeking a dedicated professional to ensure the highest quality standards in our laboratory operations. Job Responsibilities Train and become proficient in all required techniques, operation of relevant equipment, and software packages associated with testing, data analysis, and data reporting. Work with human blood, human or mammalian cell culture, and/or animals and animal tissues as needed. Complete all assigned QC tests accurately and timely under supervision, following standard protocols or operating procedures. Prioritize daily workload and develop skills to work independently. Analyze data, report test results, and complete all required documentation and database entries as required by QC protocols or operating procedures. Calibrate and maintain equipment, reporting any issues to the QC Supervisor or Manager. Maintain logs and required documentation as necessary. Prepare lab supplies, reagents, and assist with laboratory maintenance as needed. Promote a safe work environment and provide recommendations for maintaining safety. Participate in Environmental, Health & Safety programs and address corrective actions when hazards are identified. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices. Keep abreast of the basic requirements for safety compliance in your area of work and comply with those requirements. Participate in group or intra-department teams and projects as required. Engage in assigned cross-training and perform other related duties and assignments as required. Education and Experience BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years of related experience in a biotech lab environment. Experience in an industrial or research laboratory preferred. Flow Cytometry experience required. Tissue Culture experience highly preferred. Knowledge and Skills Basic computer skills: MS Excel & Word. Knowledge of general laboratory safety. Effective interpersonal, written, and oral communication skills. Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs. Effective analytical and problem-solving skills.

TempToFT We are hiring Quality Control Inspectors/Testers to join our team in Fountain Valley, CA! LONG TERM ASSIGNMENT!!! ADVANCEMENT OPPORTUNITIES!!! HIRE ON OPPORTUNITIES!!! PAY RATE: $16.00 - $19.00 ( DOE ) SHIFTS AVAILABLE: 1st Shift ( MONDAY - FRIDAY ) 6:00AM - 2:30PM 2nd Shift ( MONDAY - FRIDAY ) 3:00PM - 10:30PM JOB DESCRIPTION: Position Summary: Responsible for assigned jobs/tasks. To complete work in a timely manner with accuracy, and conformance to work instructions, IPC620/designated standards and customer requirements. Additional duties may be assigned by supervisor or department manager. Essential Duties: Execute task as assigned by lead/supervisor and/or manager Verify traveler documentation for accuracy (part numbers, revs, quantities, etc.) Verify documentation for customer inspection / test requirements Conduct inspections / test per instructions and standards Read and understand technical drawings Document all transactions per directions Refer problems or concerns to lead, supervisor or manager Maintain work area clean and organized (FOD free) Advise lead or manager of training, equipment needs and opportunities for improvement. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions SAFETY EXPECTATIONS Learn and follow all safety requirements. Failure to do so will result in disciplinary action. Maintain a clean and orderly work area. Report to work; healthy and not affected by alcohol, drugs, or other harmful influences Actively participate in safety improvement activities. Report any unsafe practices by coworkers or contractors. Immediately report all injuries and other safety incidents. AUTHORITY Communicating Problems or Opportunities for Improvement to Management for appropriate action. To report documentation requiring correction or improvement. To report any non-conforming product and opportunities for improvement. SUPERVISORY RESPONSIBILITIES: NO LIST CERTIFICATIONS AND TRAINING WHETHER OUTSOURCED OR INTERNAL IF APPLICABLE: Familiarity with IPC-620 / 610 requirements J-STD solder acceptance criteria Familiarity with PKC operating systems (QMS, Work Instructions, ERP, etc.) CORE VALUES: • Our customer's voice is at the center of everything we do. • We are committed to a vibrant, sustainable world. • Our integrity defines our value. • We respect each team member's unique abilities to drive our success. • We win through teamwork. • Our quality defines us. • Our differentiation is through innovation. Our Mission: To actively be the bridge between quality candidates and great employers! We strive to connect each applicant with great opportunities that align their respective skills in industries they are familiar with throughout the country! Who We Are: As part of our team you'll be eligable to receive: • Competitive salaries • Exceptional benefits packages • Flexible Vacation & Paid Time Off • Employer-matched 401(k) plan • Sign On Bonuses • Referral Bonuses • Great Benefits Company Description: Vantage Staffing Solutions has been noted as the fastest growing employment firm in the USA. We have helped both small & large businesses expand there operations by connecting quality job seekers through our partnerships with the best job boards on the web, curated email alerts, award-winning recruitment services, and the world's best Overall Staffing Service. Vantage Staffing Solutions is proud to be an equal opportunity employer and provides equal employment opportunities (EEO) to all employees and applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, sexual orientation, gender identity or genetics. Positions may be Temp-To-Hire, Direct Hire or Contract Opportunities and are dependent on factors including performance, attendance, safety policy adherence. Category: Staffing, Recruiting, Careers, Jobs, Now Hiring, Pay-Rolling Services, Vendor Management Services and Human Resources Management.

Autonomous Medical Devices Incorporated (AMDI) is a California-based company employing a world class team of engineers, scientists, clinicians, manufacturing and quality/regulatory experts dedicated to the development and manufacture of best in class diagnostic devices using innovative technology, factory automation, and cloud connectivity. AMDI is headquartered in Santa Ana, CA where it manufactures the Fast PCR Mini Respiratory Panel in an ISO:13485 / MDSAP certified 110,000 square foot facility. Summary of Position Are you a detail-driven professional with a passion for quality? We are seeking a Senior Quality Inspector to join our team! As a key member of the Quality team, you will play a critical role in ensuring that our products meet the highest standards of safety, effectiveness, and compliance. The Senior QC Inspector will be a hands on individual that will perform inspection and testing of incoming materials, in-process samples and finished products to ensure the materials and products conform to specifications and requirements. Communicate with team and management promptly on quality related issues. Initiate Non-conformance Report (NCR) and assist with the calibration and preventive maintenance program of equipment/instruments. Location: This is an onsite position located at our Santa Ana, CA office. Candidates living within a 25 mile range preferred. Essential Duties and Responsibilities Perform visual, dimensional, and functional inspections and/or testing across all components, subassemblies and finished medical device products using all applicable tools and equipment to ensure conformance with design specifications. Archiving receiving inspection and other QC records in Oracle PLM. Perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records. Ensuring all necessary samples are pulled and tested per procedures requirement. Determine acceptability and/or identify defective raw materials and finished products following established procedures and specifications. Provide immediate feedback to production line and immediate leadership on all quality related problems. Support the calibration and preventive maintenance program. Initiate Non-conformance Report (NCR) as needed. Additional projects and/or duties as assigned Qualifications Required for Position High school Diploma or equivalent required. Associate degree or higher preferred. A minimum of 8 years of inspection and testing experience in GMP environment, preferably in the medical device or pharmaceutical industries, is required. Proficient in a wide range of dimensional inspection techniques/equipment (caliper, micrometer, drop indicator, pin gauge, CMM, Keyence, optical inspection system) with good hand eye coordination and high manual dexterity. Contribute to and support the development of accurate and rugged inspection procedures. Able to clearly describe and convey nonconformance issues. Experienced in a fast-paced environment and able to balance and prioritize workload to support production schedule. Ability to train others in methodology and procedures. Ability to serve as a role model to other workers/colleagues in proper execution of day-to-day inspection duties as well as a guide in the understanding of operations and quality standards. Proficient computer skills in Microsoft Office Excel and Word, manufacturing software, QMS software, etc. Must be hands on and ability to as needed perform physical work pertaining to inspection Tech-savvy and able to learn new software quickly. Ability to gets things done without perfect resources, is innovative, and works with a sense of urgency. Ability to be flexible and willing to do what it takes to support company and department goals. Results oriented - drives progress & excellence. Ability to work independently with minimal supervision. Effective interpersonal and communication skills. Well organized and attentive to details. Contributes to a collaborative and inclusive work environment. An individual with high standards, takes ownership, and is invested in the outcome, is perferred. Ability to be proactively helps others, stays positive and has a good sense of humor. Work Environment The QC Inspector will work in the QC Lab, and will go to the warehouse and production floor from time to time. While performing the duties of this job, the employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk or bend and twist. The employee must occasionally lift and/or move up to 25 pounds. Salary Range The estimated base salary range for this position is $22.00 - $28.00 hourly. If the level of the role changes during the hiring process, the applicable base pay range may be updated accordingly. The actual base salary offered will be determined by several factors, including, but not limited to, the applicant's qualifications for the position, years of relevant experience, distinctive skills, and level of education attained. Autonomous Medical Device Incorporated offers a comprehensive compensation and benefits package to eligible employees including: - Company provided lunch to all employees when working at one of AMDI's on-site locations. - 401(k) match - Health insurance, 100% paid for by employer including: Medical, Dental, Vision & Life Insurance - Competitive vacation, sick days & paid holidays - Tuition reimbursement - Casual dress code - Employee discounts on activities such as theme parks, movie theaters, hotels, rental cars, etc. - Monthly company-wide socials and activities Autonomous Medical Devices Incorporated (AMDI) will not accept unsolicited resumes from any source other than directly from a candidate. An Agency must obtain advance written approval from AMDI's internal Human Resources team to submit resumes only in conjunction with approved valid fully executed contracts. Our commitment to an inclusive workplace: We are an equal opportunity employer and encourage people from all backgrounds to apply. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status, or any other protected characteristic under federal, state, or local law.

Job DescriptionOverview We are seeking a dedicated and detail-oriented Lead Quality Control Inspector to join our team in Corona, CA, 92880. In this pivotal role, you will oversee the quality control processes, ensuring that our products meet the highest standards of excellence. If you have a passion for quality assurance and a knack for leading teams, we want to hear from you! Responsibilities Lead and mentor a team of quality control inspectors, fostering a culture of quality and continuous improvement. Conduct thorough inspections of products and processes to ensure compliance with industry standards and specifications. Develop and implement quality control procedures and protocols to enhance product quality. Collaborate with production teams to identify quality issues and implement corrective actions. Analyze inspection data and prepare reports to communicate findings to management. Participate in internal and external audits, ensuring readiness and compliance. Stay updated on industry trends and best practices in quality control. Qualifications Proven experience as a Quality Control Inspector, with at least 3 years in a leadership role. Strong understanding of quality control methodologies and tools. Excellent analytical skills and attention to detail. Ability to effectively communicate and collaborate with cross-functional teams. Familiarity with industry regulations and standards. Proficient in using quality control software and tools. High school diploma or equivalent; a degree in a related field is a plus. You should be proficient in: Quality Inspection Experience ISO 13485 ISO 22000 Manufacturing Instruction (MI) FDA Regulations AS9102 Quality Control Experience Blueprint Reading Machines & technologies you'll use: Measurement Gauges Calipers and Micrometers