Quality control inspector jobs in Carlsbad, CA

Job Description Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities Perform Quality Control inspections, as required per ATEC procedures Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) Perform transactions in ERP system, as necessary to release product from Inspection Read and conform to all company policies and procedures Perform documentation evaluations Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives Assist auditors during internal audits Other duties as assigned Requirements The requirements listed below 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. Good communication skills, both verbal and written Strong organization skills and attention to detail Basic math and computer skills required Firm understanding of 21 CFR (Code of Federal Regulations), Part 820, ISO 13485, Good Documentation Practices (GDP) Firm understanding of ASTM (Association of Systems & Test Methods) standards and Heat Treat conditions per ASTM standards Experience in a controlled or regulated environment required Inspection experience with Optical Comparators, Vision Systems, hand tools Education and Experience High School Diploma or equivalent and 2-5 years of experience; experience working in a medical device industry preferred. Familiarity with quality concepts such as visual inspection and defect identification. For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate's qualifications, education, skill set, years of experience, and internal equity. $22.00 to $31.00 Full-Time Hourly Salary.

In support of, and under limited supervision of the Quality Control Supervisor, the Quality Inspector II can understand and apply the principles and several of the techniques which make up the body of knowledge recognized by those who are experts in Inspection. This body of knowledge and applied technologies include but are not limited to: The use of various Inspection Tools and Equipment, Inspection Planning and Technology, Blueprint Reading, Understanding Materials and Processes, Statistical Quality Control methods, Statistics, Sampling and Sampling Plans, Quality Audit concepts and principles, Systems Test, Packaging requirements for Commercial Optics, Training techniques. Primary Duties & Responsibilities The Inspector II has the responsibility for the action required for Assuring the quality level of the finished product, purchased materials and components are commensurate with Exotic Electro Optics requirements and customer expectations. Performing the actual physical operations of inspection, test and SPC required to provide quality control and assurance. Performing in house quality audits. Assuring the maintenance and calibration of quality information equipment and safe operating practices. Training of lower-level inspectors. Hands-on Inspection - 50% Learns to perform the following: Plan inspection workload to meet production requirements, interfacing with Production Control. Receiving inspection and test. In-process inspection. Final inspection and test. First article inspection. Quality records maintenance. Training lower level inspectors. Customer Return evaluation. Material Review support. Material Handling and Safety - 10% Become familiar with the handling practices of optical components. Able to clean optical components without causing damage. Follow Company safety rules and procedures. Tools - 20% Uses calipers, micrometers, torque wrenches, hand tools, height gauges, test plates, calculators, electronic gauges, light sources, interferometers, autocollimators, personal computers and test equipment for various products. Prints & Specifications - 10% Able to read and understand various prints, specifications, and Military Specifications. Paperwork and Recordkeeping - 10% Able to enter data into various data bases on the computer. Follow routers and work orders. File Education & Experience Minimum 2 years of related experience or a vocational or technical certificate without relative experience High School education Skills Operates Laser Marker, uses calipers, micrometers, torque wrenches, hand tools, height gauges, test plates, calculators, electronic gauges, light sources, interferometers, autocollimators, personal computers and test equipment for various products. Operational planning and scheduling of work load, Receiving inspection and test, In-process inspection, Final Inspection, Final test, First Article inspection, Quality records maintenance, Customer Return Evaluation, Material Review support. Skills in inspection, writing, interpersonal communications, and Statistical Methods necessary to perform the above functions, duties and responsibilities. Working Conditions Inspection area, gloves, masks at times, smocks Physical Requirements Standing, sitting, leaning, lifting 25-30 lbs and walking Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Aerospace & Defense, Inc.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Description: The Composites Quality Inspector is responsible for inspecting and verifying composite parts, materials, and assemblies to ensure they meet quality and engineering standards. This role involves detailed visual and dimensional inspections, the use of precision measurement tools, and accurate documentation of findings. The inspector works closely with production, engineering, and quality teams to identify non-conformances and support continuous improvement initiatives. Salary Range: $25 - $32 Duties and Responsibilities: * Perform in-process and final inspections of composite parts, subassemblies, and finished products. * Inspect for defects such as delamination, fiber misalignment, voids, surface irregularities, and bonding issues. * Use precision measuring tools (e.g., calipers, micrometers, height gauges, laser trackers) to verify part dimensions and tolerances. * Interpret technical drawings, blueprints, and specifications, including GD&T requirements. * Verify compliance with manufacturing process specifications, work instructions, and quality standards (e.g., AS9100, ISO 9001). * Document inspection results and non-conformances using appropriate forms, databases, or quality systems (e.g., NCRs, inspection reports). * Perform destructive and non-destructive testing (NDT) such as visual, ultrasonic (UT), or tap testing when qualified. * Collaborate with manufacturing and engineering to resolve quality issues and recommend corrective actions. * Support first article inspections (FAI), production part approvals (PPAP), and internal/external audits.

Acuity Inc. (NYSE: AYI) is a market-leading industrial technology company. We use technology to solve problems in spaces, light and more things to come. Through our two business segments, Acuity Brands Lighting (ABL) and Acuity Intelligent Spaces (AIS), we design, manufacture, and bring to market products and services that make a valuable difference in people's lives. We achieve growth through the development of innovative new products and services, including lighting, lighting controls, building management solutions, and an audio, video and control platform. We focus on customer outcomes and drive growth and productivity to increase market share and deliver superior returns. We look to aggressively deploy capital to grow the business and to enter attractive new verticals. Acuity Inc. is based in Atlanta, Georgia, with operations across North America, Europe and Asia. The Company is powered by approximately 13,000 dedicated and talented associates. Visit us at ****************** Work location: * This position requires on-site presence in Oceanside, CA, must report to the office every business day. Job Summary The Quality Control Technician II is responsible for reviewing incoming and in-process products using advanced inspection tools, process and established quality criteria. He/she will verify compliance of products and components through precise measurements with instruments like calipers, micrometers, and digital systems. The role involves documenting inspection results, maintaining digital records, and updating ERP quality documentation. Technicians must communicate findings, quality concerns and escalate quality issues promptly while collaborating with production, engineering, and quality teams. Additionally, they interpret engineering drawings with strong attention to details and support continuous improvement initiatives with a proactive approach. Schedule: Monday to Friday, 6:30am - 3:30pm or 7am -4:00pm Key Tasks & Responsibilities (Essential Functions) * Perform precise inspections using advanced tools (calipers, micrometers, multimeters, gauges, etc.) and

SeeScan is seeking a detail-oriented PCB/PCBA Quality Inspector to perform visual and mechanical inspections of printed circuit boards (PCBs) and printed circuit board assemblies (PCBAs). Compensation is $25 to $35 hourly. This range represents a good faith estimate based on the qualifications we expect to find in a successful candidate. Actual compensation offered may be less or greater than this estimate based on a variety of factors, including, but not limited to, our assessment of your ability to bring value to our organization. We offer * A position within an established company that has over 40 years of experience * Medical, dental, and vision coverage * Traditional and Roth 401(k) investment options, with partial company matching contribution * Flexible Paid Time Off plan with no cap or "use it or lose it" requirement In your application, include your resume and a thoughtful cover letter explaining why you are the ideal candidate for this position. We are looking for a long-term, in-house teammate to join us, not a contractor or consultant. In this position, you will * Perform incoming, in-process, and final inspections of PCBs and PCBAs according to drawings, assembly instructions, and applicable standards * Inspect solder joints, component placement, polarity, and labeling using magnification tools and microscopes * Review and interpret engineering drawings, BOMs, and schematics * Identify, document, and report nonconformances, assisting with root cause analysis and corrective actions * Collaborate with manufacturing engineers and technicians to address rework, repair, and process improvements * Ensure all inspection results and quality data are accurately recorded * Maintain a clean, organized, and safe work environment * Support calibration and maintenance of inspection tools and equipment Your background * 3+ years of experience in electronic assembly inspection, preferably in a manufacturing or OEM environment * Familiar with electronic components, assemblies, and soldering processes * Able to read and interpret schematics, assembly drawings, and BOMs * Experience using inspection tools such as microscopes, calipers, and multimeters About you * Excellent attention to detail and accuracy * Strong communication skills, with the ability to work collaboratively in a team-oriented environment * Comfortable working in a fast-paced manufacturing environment About SeeScan Beneath the ground and below the water's surface is a world out of sight. Whether it's the inside of a pipe, or a maze of the buried services that keep our world running, or the deepest places of the ocean, our mission is to create products that help our customers see. Dating back more than 40 years to our founder's garage, we are an original equipment manufacturer in San Diego, CA that builds diagnostic, utility locating, and harsh-environment oceanographic equipment from the ground up. And as leaders in our industries, we provide ongoing support and parts services to ensure that our equipment is never short of the best. At SeeScan, you'll be part of a group of people who bring passion and energy into everything they do. We value the individual contributions all of our employees make and invest in the tools and training they need to find success and professional growth. We do our best to empower the right people to take on new opportunities, and our culture promotes transparency, integrity, and continuous learning. Notes * No recruiters, contractors, or consultants, please * No relocation assistance or visa sponsorships available for this position * SeeScan is an Equal Opportunity Employer

GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection * Receiving inspection of components following procedures, specifications and drawings. * Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. * Read engineering drawings and interpret geometric dimensioning and tolerancing. * Review associated paperwork, complete inspection records using good documentation practices, and release components. * Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) * Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) * Carefully handle and process extremely small components without damaging them. In-Process Inspection * Perform Line Clearance for Operations activities * Inspect and release labeling * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform inspections on components and assemblies in manufacturing Final Inspection * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform final inspection on finished goods * Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. * Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing * Perform in-house peel testing on sealed packages * Maintain sample retain area Other Duties * Work with engineering in the design of high quality inspection / metrology fixtures. * Support equipment and process validation activities by inspecting process outputs * Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. * Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. * Coordinate the monthly environmental monitoring of the cleanrooms. * Coordinate quarterly dose audits. How will you get here? * High School Diploma required. * 0-2 years industry experience. Knowledge, Skills, and Abilities * Medical device experience and working knowledge of QSR a must * Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable * Attention to detail and accuracy a must * Must have excellent documentation skills * Team player, good written/oral communicator * Must be organized and able to coordinate activities with outside vendors #GKOSUS

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. What you can expect in this role: As a Quality Inspector at nVent Management Company, you will be part of a team known for their hard-working approach in delivering top-tier electrical and data center solutions. You will encounter: * Performing comprehensive product inspections based on criteria defined in work instructions, checklists, and drawings. * Prioritizing tasks as established by the Operations Supervisors to maintain efficiency and meet departmental deliverable goals. * Identifying non-conforming products that do not meet predefined requirements. * Crafting Non-Conformance Reports (NCRs) in response to discoveries of non-conforming products. * Ensuring there are no active NCRs before completing a product inspection to maintain strict quality control and compliance. * Applying precision and non-precision gauges, meters, tools, or devices to determine conformance to the relevant acceptance criteria. You have: To compete for this role successfully, you have: * High school diploma or G.E.D. * Candidates with 1 year of experience in quality processes and familiarity with Quality Management Systems are preferred. * Ability to use precision measuring equipment (e.g., Calipers, micrometer, paint mil gauges, hardness tester, CMM, measuring tables, optical comparators, functional testers, etc.). * Ability to effectively coordinate, plan workload and work in a self-directed manner. * Ability to apply strong written and verbal communication skills, with the ability to collaborate with individuals across various functional areas within the company. * Ability to interpret and apply Quality System / ISO procedures and documentation. * Skills to quickly learn and operate a wide variety of test and measurement equipment. * Skills in attention to detail and accuracy. * Ability to apply appropriate math and geometry. * Skill in using personal computers including Microsoft Office applications (Word, Excel, etc.). WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $17.20 - $31.90 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

The Vision System Operator is responsible for the operation of the Mitutoyo Vision System and the programming of the system. This position will write, develop and validate vision measuring system using QVPAK. Responsible for interpreting technical documents, engineering blueprints and 3D CAD models into precise measurements. Additionally, this role will perform first article inspections and complete non-conformance documentation working in coordination with Quality Control for the enhancement of processes and procedures. Responsible for the programming and operations of the Mitutoyo Vision System, including: Creating inspection program by writing, developing and validating new inspection programs for the Vision measuring system using software such as QVPAK Interpretation of technical documents including the translation of complex engineering blueprints, technical drawings and 3D CAD models into precise measurement routines. Fixture and calibrate, setting parts on the vision system, ensuring proper fixture and perform regular calibration checks to guarantee accuracy and reliability Collaborate with Design and Manufacturing Engineers to determine measurements and develop efficient inspection plan. Responsible for the operation and inspection, including Running automated and manual measurement program to perform first-article inspections Using the vision system's capabilities, including optical, laser and touch probes to inspect intricate shapes and tight tolerances Analyze measurement data and create comprehensive inspection reports, including First Article Inspection Reports (FAIRs) and non-conformance documents. Identify and resolve program errors, measurement discrepancies and system performance problems. Work within Quality Management System (ISO 9001) to ensure all inspections are compliant Perform supplementary dimensional inspections with manual tools such as micrometers, calipers and height gauges, etc. Other duties as assigned. KPI Reporting Responsibilities As established with Director of Quality Control Job Qualifications, Skills, and Abilities Minimum of associate's degree in technical field such as Manufacturing Technology, Metrology or related degree, preferred 3-5 years hands on experience with precision manufacturing environment. 1-3 years' experience as a Quality Inspector preferred. Prior experience using a Mitutoyo Vision Machine with QVPACK preferred Knowledge of MiCAT Planner software a plus Advanced ability to read and interpret complex engineering blueprints and able to apply Geometric Dimensioning and Tolerance (GD&T) principles Working knowledge of Microsoft Office Working knowledge of NetSuite a plus Excellent verbal and written communication skills preferred Travel Expectations 0% Physical Activities may include sitting and standing for long periods of time. Able to use eyes for visual inspections, able to navigate a small work area. May work on a computer for long periods that may emulate blue light.

AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. Comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. JOB SUMMARY: The Quality Inspector inspects a range of components, parts and/or products for the area assigned as prescribed by all applicable specifications and quality assurance Instructions. Identifies moderately difficult quality issues in design, process or other inefficiencies to meet quality requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards. Participates in analysis statistical data from processes to either confirm compliance with established standards or identify deviations from standards. Performs visual inspections of soldered connections, mechanical inspections of electronic and electro-mechanical assemblies and subassemblies. Prepares and completes all necessary documentation for reporting. Acceptance/rejection of inspected and/or tested items. Identifies design, process or other inefficiencies and reports quality concerns and issues. Performs routine quality inspections on engineering designs, assemblies, piece parts, final assemblies and tooling. Conducts Internal audits and corrective action follow ups. Other responsibilities as assigned. Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary. JOB SPECIFICATIONS: Education: High School Diploma or equivalent. A Secondary Certificate combination of relevant education and work experience that will allow successful performance of job expectations. Certifications: Vocational training, apprenticeships, or the equivalent experience in related field. Experience: 2- 5 years of relevant experience. Skills: Ability to follow established job instructions and procedures with minimal supervision. Able to apply a systematic QA approach while using existing procedures to solve a range of technical issues. Skilled at measuring and using test equipment as prescribed by job assignment. Capable of following instructions and applying processes and procedures to standard routine tasks Must be able to interpret and follow written and verbal instructions, including engineering drawings, charts, diagrams, and sketches. Proficient computer skills. Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $20.10/hour- $30.10/hour. Axillon is an Equal Opportunity and Affirmative Action Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position is subject to meeting export compliance eligibility requirements. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. (“Minority / Female / Disability / Veteran / VEVRAA Federal Contractor”) If you would like more information about Equal Employment Opportunity as an applicant under the law, please go to Know Your Rights: Workplace Discrimination is Illegal (eeoc.gov) and Genetic Information Discrimination

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Us:** Teledyne Marine's technology is used to monitor and explore almost everything below the sea's surface. From addressing environmental needs and preserving safety and peace, to solving challenges with infrastructure and energy source development, the work we do today is making a difference for tomorrow. For more information, visit our website at: teledynemarine.com **You:** If you're the best at what you do and are looking for an exciting opportunity to share your unique talents in a fast-paced environment, please apply now! By joining Teledyne Marine, you will be part of an innovative team of scientists, engineers and operators designing and manufacturing best-in-class marine sensors, instruments and vehicles. You will have access to state-of-the-art labs and equipment to take cutting edge design from concept through development and integration to its final application in the real world. **General Overview** The Product Quality Inspector performs product inspection and/or audits of quality control programs. Performs manufacturing inspections, and sampling and testing of incoming components and raw materials. Inspects and tests product manufactured or processed by suppliers to ensure conformance to requirements and specifications. Identifies material and processes as Conforming or Nonconforming. Writes simple reports of findings for review. Tasks may include complex and/or non-routine assignments. **Essential Duties and Responsibilities** include the following. Other duties may be assigned. + Perform incoming inspection of mechanical assemblies, electrical assemblies, PCBA's, sub-assemblies, and parts + Coordinate MRB activities related to nonconforming product, including generation of Non-Conforming (NC) Reports + Perform in process audits + Coordinate activities related to incoming inspection: incoming inspection priorities + Review and approve Certificate of Conformance (COC) + Support calibration program and processes + Conduct shipping audits + Notify errors on procedures, drawings, bills of material, and router to the support teams (Quality, Manufacturing Engineering, etc.) + Responsible for completing documentation (shop order, etc.) accurately and timely + Responsible for entering data into the IFS system accurately and timely + Responsible for maintaining high quality standards and workmanship + Maintain excellent communication and working relationship with all departments within the company + Maintain a safe working environment + Communicating special tooling needed to perform operation that may have not been identified + Working knowledge of Microsoft tools such as Excel and word **Supervisory Responsibilities** This position does not supervise other employees. **Qualifications/Requirements** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below 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. **Education/Experience** + High school diploma or equivalent. An Associate's degree is preferred. + Minimum 2-4 years of related experience in mechanical, PCBA's and electro-mechanical assemblies or equivalent combination of education and experience. + At 2+ years of experience in IPC 610 requirements is highly preferred. + Understanding of inspection techniques, reading, writing and basic arithmetic skills + Ability to interpret blueprints, schematics and perform complex measurements using advanced measurement tools and equipment + Experience with mechanical housings built to tight tolerances (.001") + Special Process experience - anodize, paint, urethane, epoxy, casting preferred + Experience with cable assemblies built to IPC requirements + Experience with Coordinate Measuring Machine (CMM) and Eddy Current meter preferred + Experience using a microscope, multimeter, calipers, height gages, material analyzers, surface measurement tools, time domain reflectometer (TDR) and miscellaneous electrical equipment **Salary Range:** $42,800.00-$57,100.000 **Pay Transparency** The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position. Teledyne conducts background checks on qualified applicants who receive a conditional offer of employment in accordance with applicable laws, regulations and ordinances. Background checks may include, but are not limited to, education verification, employment history and verification, criminal convictions, Motor Vehicle Report (MVR & driving history), reference check, credit checks/credit history and drug testing. All qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. We have the need for a First Shift Quality Inspector to join our Poway, CA team. Under limited supervision this position is responsible for inspecting a wide variety of parts, assemblies, tooling fixtures and material to ensure compliance with customer requirements, company specifications, and quality requirements. Sets up, operates, inspects, tests, and adjusts new and reworked tools, dies, gauges, jigs and fixtures for conformance to engineering drawings and specifications. Maintains, processes, and compiles a variety of confidential and sensitive electronic and hard copy reports, records and statistics. Assignments are typically non-routine where judgment and assessment are required to resolve moderately complex issues. May conduct inspections at customer or vendor sites. DUTIES AND RESPONSIBILITIES: Inspects machined parts, components, assemblies and materials to ensure compliance with appropriate regulatory guidelines (Military Standards, ASTM and ANSI, and ASME Code). Provides various electronic and hard copy reports of inspections and notifies appropriate parties including project engineers. Sets up and calibrates measuring and test equipment and schedules service and repair of equipment. May prepare, update and maintain calibration computer databases. May perform non-destructive test (NDT) on various metallic and non-metallic materials, parts and assemblies using a variety of methods and techniques such as radiography, helium leak testing, and/or ultrasonic testing. May observe testing and provide oversight, as necessary, to verify compliance with requirements. May interact with and provide responses to regulatory agencies and customers during their audits and review of company inspection and calibration activities. May monitor and verify quality in accordance with statistical process or other control procedures. May coordinate the procurement of standard materials, services and parts for inspections. Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Typically requires an associate's degree, trade school certificate, military training or equivalent in quality inspections or certification by a professional group such as ASQ or AWS, and one or more years of progressive experience in electrical, mechanical, electromechanical or metrology inspection and calibration. May substitute additional experience in lieu of formal education and training. Must possess: ability to read and understand engineering drawings and specifications, and perform mathematical computations good communication skills to effectively interface with all levels of employees including management ability to interpret complex information and respond to a variety of complex issues ability to maintain the confidentiality of sensitive information good computer skills. Ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Must be able to adapt to various working conditions such as heights, high voltage electricity or radioactive materials. Experience with ISO 9001, DOE quality assurance program requirements, and nuclear material are desirable.

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.

Job Details Irvine, CA Full Time High School $25.00 - $25.00 HourlyDescription Job Title: Inspector, Quality Control Supervisor/Manager Title: Staff Engineer, Quality (Production Support) Job Description Summary: Responsible for supporting the Quality department with quality control activities related to the manufacture of the THV within the Leeds and Irvine production facilities. To include in-process and final inspection, labelling/packaging, documentation, and environmental monitoring. The role holder will also provide routine reports and communications to provide timely updates on inspection status. Job Responsibilities: Conduct routine testing on THV, to include functional, visual, and final inspection processes, along with supporting sterilization preparation. Perform Microbiological monitoring on ViVitro (Leeds) or BDC (Irvine) when required. Conduct Preventative Maintenance and calibration of the ViVitro (Leeds) or BDC (Irvine) equipment. Conduct audits on the in-process paperwork associated with the manufacturing process including, but not limited to: manufactured valve DHRs, Jasmine preparation and ancillary logs. Provide support to the Engineering staff by gathering data on clinical product to allow decisions to be made on functionality. Adhere to Quality System and record retention requirements. Comply with all site Health & Safety requirements. Contribute to continuous improvement efforts related to valve manufacture and inspection processes. Inspect final packaging labels and confirm they are applied correctly per the relevant standards and Work Instructions. Support other areas of the business as necessary and applicable to the role. Qualifications Required Education and Experience: A-Levels, or equivalent and substantial relevant practical experience, in science related subjects are required. Bachelor's degree in a division of Biology, Chemistry or a Biomedical related discipline is desired (Leeds). Minimum of 3-5 years' experience in Quality within the medical devices or pharmaceutical industries is desirable. Must be familiar with 21CFR820 and ISO 13485 requirements. Hands on experience with these requirements is preferred. Experience assessing products for compliance and final release is desirable. Skills and Abilities Required for This Job: Must be able to work effectively and collaborate within cross-functional teams. Must possess the ability to handle multiple tasks, with high attention to detail. Ability to file and organize records in a compliant, easily retrievable manner. Must be able to effectively articulate (verbally and in writing) results and conclusions. Must have good documentation skills. Must be able to take initiative and work autonomously with the ability to prioritize a workload.

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 DescriptionSalary: $30/hr + DOE OrthAlign, Inc., a Smart Technologies, growing medical device company, has an immediate opening for aSr. Quality Control Inspector. This role supports all quality initiatives and is responsible for quality control inspection of incoming materials and in-process manufacturing. This position supports audits and reviews/analyzes data and documentation. You will: Perform dimensional, visual and functional inspections of raw materials, components, finished assemblies and in-process manufacturing work. Document inspection results clearly and completely. Disposition materials and enter transactions in our ERP system. Review supplier test results and First Article Inspections (FAI) reports. Support RA/QA associates on defect awareness, inspection methods and specification requirements. Maintain knowledge of all procedures and changes to specifications related to areas of responsibilities. May perform First Article inspections. Review Device History Records (DHRs) for product release. Write and distribute non-conformance reports (NCMRs) for nonconformances found during inspection. Inspect various plastic and metal components, mechanical instruments, circuit boards, electro-mechanical assemblies, labels and packaging materials You need: 6+ years Inspection experience in medical device or similar industry (i.e., aerospace, automotive or other highly technical, regulated and rapid-paced environment) Excellent written and verbal communication skills Ability to work as a collaborative team member as well as independently Flexibility and strong organizational skills with ability to prioritize multiple tasks Experience using calipers, micrometers, height gages, gage blocks, microscopes and similar inspection tool Experience with ERP / MRP software systems, especially conducting material transactions Ability to initiate and manage time effectively without direct supervision To know howto read and interpret engineering drawings, ANSI-Y-14.5 Dimensioning and Tolerancing Sound judgment when making decisions and communicating with peers and management Excellent attention to detail, producing high quality output appropriate To be results-oriented with appropriate urgency and follow-up We offer: Competitive compensation including bonus and equity Opportunities for career advancement Full benefits package An evolving, engaging culture and workplace Nominated by our employees as aTop Place to Work in Orange County! It is an exciting time at OrthAlign - make your next career move with us! Please note that we are unable to provide any type of sponsorship at this time.

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 QC Inspector's primary responsibility is to verify conformance of product to customer requirements and specifications through product inspection by 100% visual and/or dimensional measurement and product testing as well as the required secondary operations. Responsibilities: Inspection of product for visual defects via unaided eye or some magnification Inspection of product for dimensional specifications using contact and non contact measurement equipment Trimming of product to remove excess flash Perform required secondary operations such as part washing, drying, packaging Documentation of inspection results Qualifications: must be able to perform each essential duty satisfactorily Understanding the importance of product conformity Ability to read and write in English and/or Spanish Understand lot number identification and traceability Organized, neat and meticulous Able to perform repetitive tasks efficiently Good communication and interpersonal skills Basic math skills Perform other duties, as required Previous inspection experience is preferred Minimum of High School level of education is required Ability to handle moderate lifting, no greater than 50 lbs

Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities * Perform Quality Control inspections, as required per ATEC procedures * Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) * Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred * Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed * Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms * Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) * Perform transactions in ERP system, as necessary to release product from Inspection * Read and conform to all company policies and procedures * Perform documentation evaluations * Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives * Assist auditors during internal audits * Other duties as assigned

OrthAlign, Inc., a Smart Technologies, growing medical device company, has an immediate opening for a Sr. Quality Control Inspector. This role supports all quality initiatives and is responsible for quality control inspection of incoming materials and in-process manufacturing. This position supports audits and reviews/analyzes data and documentation. You will: Perform dimensional, visual and functional inspections of raw materials, components, finished assemblies and in-process manufacturing work. Document inspection results clearly and completely. Disposition materials and enter transactions in our ERP system. Review supplier test results and First Article Inspections (FAI) reports. Support RA/QA associates on defect awareness, inspection methods and specification requirements. Maintain knowledge of all procedures and changes to specifications related to areas of responsibilities. May perform First Article inspections. Review Device History Records (DHRs) for product release. Write and distribute non-conformance reports (NCMRs) for nonconformances found during inspection. Inspect various plastic and metal components, mechanical instruments, circuit boards, electro-mechanical assemblies, labels and packaging materials You need: Ÿ6+ years Inspection experience in medical device or similar industry (i.e., aerospace, automotive or other highly technical, regulated and rapid-paced environment) Excellent written and verbal communication skills Ability to work as a collaborative team member as well as independently Flexibility and strong organizational skills with ability to prioritize multiple tasks Experience using calipers, micrometers, height gages, gage blocks, microscopes and similar inspection tool Experience with ERP / MRP software systems, especially conducting material transactions Ability to initiate and manage time effectively without direct supervision To know how to read and interpret engineering drawings, ANSI-Y-14.5 Dimensioning and Tolerancing Sound judgment when making decisions and communicating with peers and management Excellent attention to detail, producing high quality output appropriate To be results-oriented with appropriate urgency and follow-up We offer: Competitive compensation including bonus and equity Opportunities for career advancement Full benefits package An evolving, engaging culture and workplace Nominated by our employees as a Top Place to Work in Orange County! It is an exciting time at OrthAlign - make your next career move with us! Please note that we are unable to provide any type of sponsorship at this time.