Quality control technician jobs in Thousand Oaks, CA

About Us Haskel, an Ingersoll Rand Company, is a High-Pressure Technology Solutions. We specialize in Air-Driven Liquid Pumps, Air-Driven Refrigerant Pumps, Hydraulic Drive Compressors, Gas Booster Compressor System, BuTech High-Pressure Valves and Hydrogen Valves Fitting and Tubing. Job Summary This role is responsible for ensuring the quality control cell is actively engaged to meet daily customer demand and production schedule. Performs receiving, in-process and/or final inspection of hardware. Conducts complex inspections as defined by quality/inspection plans or per directions of quality management/engineering. Uses a complete range of precision tools and instruments requiring advanced inspection skills and techniques. Ensures that all gauges/tools used are properly calibrated. Identify accurate and efficient means of inspection techniques. Works with general/minimal supervision. Train and provide directions to the Quality Control team under the supervision of the Quality Control Manager. Responsibilities The Quality Team Lead will inspect products by using a variety of inspection tools/devices, work instructions and computer to perform a series of inspections to correctly verify incoming parts, in-process and completed assemblies. Verify supplier material certifications, including special processes, and ensure compliance with quality/PO requirements. Creates supporting documentation (data books, certificates of conformance, etc…) Support disposition of discrepant materials (MRB) in accordance with appropriate quality procedures and maintain low inventory of on-hold parts. Verifies first articles from suppliers and internal departments. Prepares and processes records and reports to document supplier/operations performance. Qualify supplier components and/or systems for assuring conforming product. Adheres to calibrations system of inspection, measuring and test equipment. Applies Statistical Quality Control techniques as directed. Assist with interpretation of drawings, specifications and quality requirements. Properly process goods for outside processing, investigates and evaluates component parts returned and nonconforming product. The Quality Team Lead provides effective training to the quality control cell and ensures safety and quality standards are always maintained. Work with supervisor to manage and prioritize staffing assignments to ensure customer demand and the production schedule are met. Use basic problem-solving skills to ensure stable operation of the quality control cell. Report problems or concerns with quality, processes, equipment, materials and labor to Quality management. Work closely with support staff such as Purchasing/Planning, Manufacturing Engineering, Production Supervisor, Materials/Warehouse to resolve issues. Observe, maintain, coordinate and complete standard work. Update production metrics and facilitate regular team communication. Identify and support continuous improvement efforts with Quality management. Sustain and drive lean manufacturing and 5S activities. Follow documented policies and procedures as designated by the company's Quality System. Basic Qualifications Ability to read and interpret documents such as safety rules, engineering drawings, operating and maintenance instructions, Material Standards, Quality Plans, Control Plans and Inspection Test Plans. Experience with Microsoft Office (Word, Excel, Outlook). Ability to communicate effectively through oral and written communications. Ability to analyze and solve problems. Ability to work with others collaboratively. Strong organizational skills. Preferred Experience leading teams or projects strongly desired. Quality Control experience. Lean manufacturing and continual process improvement experience. Educational Requirements High School diploma or equivalent Five years + of related experience and a minimum of two leading teams. LIP Eligible Role This position is eligible for the LIP (Local Incentive Plan) of up to 4%. The pay range takes into account a wide range of factors that are considered in making compensation decisions including, but not limited to, skills; experience and training; licensure and certifications; and other business and organizational needs. The disclosed pay range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Ingersoll Rand, it is not typical for an individual to be hired at or near the top of the pay range for their role and compensation decisions are dependent on the facts and circumstances of each case. At Ingersoll Rand, we think and act like owners - of our business, our communities, our planet, and our health too. The Ingersoll Rand benefits program provides you with the tools and resources to take accountability for your health so that we can continue to help make life better. Benefits of employment and include; Medical and Prescription drug plans Wellness and Chronic disease management programs Dental, vision, life/AD&D insurance Short- and Long-term disability Health Savings Account Flexible Spending Account Parental Leave Employee Assistance Program Discount Program Employee Stock Grant 401k plan with a company match 3 weeks of paid vacation and 11 paid holidays throughout the calendar year Voluntary benefits include legal, accident, and critical illness protection

Quality Control Inspector Needed in Camarillo Direct Hire Industry: BioTech, Pharmaceuticals Pay range: $23 - $24/hour Monday - Friday 7am - 3:30pm Must Have * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. Job Summary Performs quality control inspections in all aspects of operations, checks, and test during the manufacture of products. Inspect incoming materials, and products at different stages of production. Records observations and make recommendations for improving processes. Essential Functions * Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements; * Conduct inspection and testing related to: ► Incoming product. ► First article. ► In-process. ► Final. * Initiate nonconformance reports (NCR). * Performs all aspects of testing related to manufacturing. o Incoming inspections o In-process inspection. o Final Inspection release of finished goods. o Document review. o Supports cross functional departments investigate potential non-conformance's observed * Ensures that all inspections and procedures are properly completed and documented. * Perform pre and post-inspection of product gamma irradiation process. * Approve or reject raw materials with respect to quality standards and communicate results to all pertinent parties. * Initiate nonconformance reports (NCR) for all non-conforming material identified throughout operations * Prepare and submit Metrics reports to the quality supervisor or QC lead * Comply with all safety requirements ensuring work areas meet standards. * May be required to report to multiple facilities within a 2-mile radius. * Job Order document review and release * Other duties as assigned Education * High School Diploma or equivalent with 2 years of experience in quality control inspections. Required Experience & Competencies * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. * Solid organizational and planning skills required. * Ability to communicate effectively, verbally and in writing, demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors. * Must be able to work effectively and efficiently in a team environment. * Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction. * Must display personal accountability for results and integrity. * Must display eagerness to learn and continuously improve. * Must have uncompromising dedication to quality. * Good general mathematical skills. * General knowledge and use of measuring devices such as calipers, tape measures, rulers, pin gauges * General computer skills. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Department: Cardiac Cath Lab FLSA Status: Non-Exempt - 12 week Contract Shift: 8 hours, Days Join Premier Healthcare Staffing as a Certified Cath Lab Tech and step into a high-impact, day-shift contract where your expertise truly matters. You'll work alongside a skilled cardiovascular team, operate advanced technology, and play a vital role in delivering life-saving care-all within a supportive environment that values your experience. Enjoy competitive pay while elevating your career and making a difference from day one. EDUCATION, EXPERIENCE, TRAINING Requires previous experience assisting with scrubbing procedures in a Cardiovascular Lab. ARRT-R and license required Cardiovascular technician training program with emphasis in invasive cardiology and hemodynamic monitoring. BCLS (AHA) required upon hire and maintain current. Advanced Cardiac Life Support (ACLS); required. Proficient computer skills. Premiere Healthcare Staffing is here to help you on your career journey! We place talented candidates with our partner healthcare facilities with the shared goal of providing exceptional, compassionate care. Award-winning hospital partners across the nation Dedicated career specialists to support you every step of the way Immediate and flexible opportunities to create your career journey Tailored career pathway where you can thrive personally and professionally

This role is designed for Second Shift. The Quality Technician II supports the Quality Engineering group through processing First Article Inspection (FAI) and Part Approval Process, selective inspection, analysis and processing of internal Nonconformance Reporting (NC) material and other administrative and logistical support duties. Represents the Quality Department in witnessing and documenting UAV flight acceptance test activity. Position Responsibilities Processes inbound or outbound FAI and deliverable submissions accurately and timely including: receipt and analysis of parts and/or supporting documentation; completion of associated records and logs; communication of submission status as needed to QEs, managers, engineers or interested parties; processing of parts after completion; maintaining records and files associated with submissions; and other related tasks. Conducts selective inspection under the direction of the QE group including: receipt and verification of material, completion and maintenance of related documentation, communication of inspection results to concerned parties and processing of material after verification using Agile/Oracle database. Processes internal non-conforming material as needed in support of QE including: retrieval and analysis of material, interpretation of preliminary findings and restatement of problem statements to ensure understanding of problem, processing material through the necessary NC processes, communication of status to concerned parties, maintaining necessary documentation and processing material to internal and external suppliers. Provides general support of QEs including communication, Corrective Action Request processing, product evaluation, and sorting activities under exceptional circumstances, and interfacing with other team members as necessary to complete assigned tasks in support of continuous improvement initiatives using A3, Six Sigma DMAIC forms. Support DCMA Source Inspection process Coordinates with Shipping and Contracts department as needed to ensure timely delivery. Responsible for creating the Final Inspection documentation package including COC, TDR's, etc., and as necessary support internal/external customer inspection. Represents and supports QEs during internal and 3rd party audits regarding the essential functions above and as needed regarding our measurements system and documented system. Develops and maintains process instructions for quality-related activities Works on assignments that are semi-routine in nature Other duties as assigned Basic Qualifications (Required Skills & Experience) High School Diploma or GED equivalent 1 - 2 years of related work experience or equivalent combination of education, training, and experience Demonstrated expertise in mechanical inspection methods and skills including surface plate work, hand tools, and gages, etc. Solid ability to read and understand drawing requirements including a solid understanding of Geometric Dimensioning and Tolerance to ANSI Y14.5 Basic knowledge of FAI validation and verification process requirements Strong computer skills and is proficient in MS Office Suite (Word, Access, PowerPoint, Excel) Basic knowledge of engineering drawings and specification systems Must be able to fill out the necessary flight test documentation Must be able to properly document any/all non-conformances encountered Must have the skills necessary to perform pre and post-flight visual inspections on flight hardware and components. Must possess the skills necessary to remove and replace field replaceable components on aircraft. Will populate excel spreadsheets on a daily basis documenting flight test results Must able to work efficiently in a fast-paced, high-volume environment Required to travel to and from remote flying sites on a daily basis Must have a valid California driver's license and clean driving record Willingness to work overtime also a must Other Qualifications & Desired Competencies 2 year technical degree desired; Quality system courses and/or equivalent experience preferred Aerospace quality management system experience (AS9100DD) and/or internal audit experience is preferred Solid ability to accurately record and manage data, records, files and other documents to support tasks Has an analytical approach to problem solving and high organizational skills as well as effective time management, interpersonal and communication skills Strong ability to manage time and prioritize tasks Able to excel in a fast-paced, deadline-driven environment, where small teams share a broad variety of duties Displays strong initiative and drive to accomplish goals and meet company objectives Takes ownership and responsibility for current and past work products Is committed to learning from mistakes and driven to improve and enhance performance of oneself, others, and the company Focuses on teamwork, collaboration and puts the success of the team above one's own interests Physical Demands Ability to work the majority of the time outdoors in varying weather conditions, when needed, during flight test activity (Frequent) Ability to lift up to 50 lbs. and carry/move objects of varying shapes and sizes (Frequent) Regularly required to, stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard (Frequent) Clearance Level Clearance Level AeroVironment considers several factors, including but not limited to, the location, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. ITAR Requirement: T his position requires access to information that is subject to compliance with the International Traffic Arms Regulations (“ITAR”) and/or the Export Administration Regulations (“EAR”). In order to comply with the requirements of the ITAR and/or the EAR, applicants must qualify as a U.S. person under the ITAR and the EAR, or a person to be approved for an export license by the governing agency whose technology comes under its jurisdiction. Please understand that any job offer that requires approval of an export license will be conditional on AeroVironment's determination that it will be able to obtain an export license in a time frame consistent with AeroVironment's business requirements. A “U.S. person” according to the ITAR definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee or asylee. See 22 CFR § 120.15. Some positions will require current U.S. Citizenship due to contract requirements. Benefits: AV offers an excellent benefits package including medical, dental vision, 401K with company matching, a 9/80 work schedule and a paid holiday shutdown. For more information about our company benefit offerings please visit: ********************************** We also encourage you to review our company website at ******************** to learn more about us. Principals only need apply. NO agencies please. Who We Are Based in California, AeroVironment (AVAV) is a global leader in unmanned aircraft systems (UAS) and tactical missile systems. Founded in 1971 by celebrated physicist and engineer, Dr. Paul MacCready, we've been at the leading edge of technical innovation for more than 45 years. Be a part of the team that developed the world's most widely used military drones and created the first submarine-launched reconnaissance drone, and has seven innovative vehicles that are part of the Smithsonian Institution's permanent collection in Washington, DC. Join us today in developing the next generation of small UAS and tactical missile systems that will deliver more actionable intelligence to our customers so they can proceed with certainty - and succeed. What We Do Building on a history of technological innovation, AeroVironment designs, develops, produces, and supports an advanced portfolio of unmanned aircraft systems (UAS) and tactical missile systems. Agencies of the U.S. Department of Defense and allied military services use the company's hand-launched UAS to provide situational awareness to tactical operating units through real-time, airborne reconnaissance, surveillance, and target acquisition. We are proud to be an EEO/AA Equal Opportunity Employer, including disability/veterans. AeroVironment, Inc. is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Qualified applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, protected veteran status, genetic data, sexual orientation, gender identity or other legally protected status. ITAR U.S. Citizenship required

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. The Quality Assurance Technician is responsible for ensuring that products or services consistently meet defined quality standards and customer requirements. They perform inspections, tests, and evaluations to identify and resolve quality issues, contributing to the overall quality of the production process. JOB QUALIFICATIONS: High School Diploma or equivalent required 2-5 years of experience in related field Knowledge of FDA/cGMP guidelines, 21 CFR Parts 111, 210 & 211 preferred Highly organized and strong attention to detail Time management skills and ability to handle multiple tasks on time Excellent oral and written communication skills in English Proficient in Word and Excel Working knowledge of Oracle and Agile preferred Experience with Warehouse Management Systems (WMS) Must be able to drive a forklift, training offered POSITION RESPONSIBILITIES: Manage receiving inspection of all critical components and raw materials Manage and support JIT program Review and report all documentation from shipments prior to release in Oracle Manage NCMR and RMA programs and oversee trailer loading or products slated for destruction Manage physical inventory in NCMR and Quality Cages Write and Review CRNs/NCMRs/CAPA/Investigations/Deviations as needed Maintain the retains program and storage of retains Perform and manage annual review of Finished Good retains Generate reports to look for trends in inspections Suggest solutions to management for trends when required Work with cross-functional departments Assist with investigations as requested QA inquiries from other sites or vendors Train the team on processes as needed Assist Quality Management as needed Physical Requirements: Walking up to 6 hours per day Sitting up to 2 hours per day Occasionally lift up to 30 lbs. Salary Range: $21.50-$22.50/hr BENEFITS: PLD is a proud employer offering many corporate benefits, including: ⠁ Medical and Dental Benefits ⠁ Vision ⠁ 401K with employer match ⠁ Group Life Insurance ⠁ Flex Spending Accounts ⠁ Paid Time Off and Paid Holidays ⠁ Tuition Assistance ⠁ Corporate Discount Program ⠁ Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity 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.

Huntsman is seeking a Quality Control Technician supporting the Huntsman's Advanced Materials Division located in Los Angeles, California. This position will report to the Quality Control Manager. Job Scope The Quality Control Technician performs accurate and timely routine testing of lab samples and reporting in accordance with specified technical methods and environmental, health and safety. guidelines. In summary, as the Quality Control Technician, you will: Perform accurate and timely inspections and testing of samples of raw materials, intermediate and finished goods. Maintain quality control records, including data entry into notebooks, logs, LIMS / Labworks software and ERP / SAP software. Issue timely notifications of nonconforming results as appropriate. Maintain retained samples and prevents detrimental exposures and contamination. Maintain traceability and retrievability of retained samples. Properly replenishes retained samples when running low. Maintain lab instrumentation, equipment and tools in safe and good working condition. Submit service, calibration or repair work orders when required. Be responsible for maintaining adequate inventory of reagents and lab supplies through prompt restocking requests to avoid shutdown. Maintain a clean and orderly workplace in accordance with Company requirements. Attend and participate in regular meetings. Complete periodic quality refresher and environmental health and safety training. Participate in continuous improvement initiatives. Qualifications You must possess the below minimum qualifications to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates. The candidate must have an unrestricted right to work for Huntsman in the United States. Minimum Qualifications Minimum associate degree of science in chemistry or a related field with hands-on laboratory coursework. You must be willing and able to work any of the three shifts (1st, 2nd, or 3rd) based on business needs. 1st Shift Hours - 6:00 a.m. - 2:30 p.m. 2nd Shift Hours from 2:00 p.m. - 10:30 p.m. 3rd Shift Hours from 10:00 p.m. - 6:30 a.m. Laboratory work experience demonstrating proficiency in wet and analytical chemistry, handling strong acids, strong bases, and organic solvents. Experience with industrial adhesives testing preferred but not required. Experience with mechanical testing is preferred but not required. Working knowledge of safe lab practices. Know-how and Skills Skills and knowledge Strong verbal and written communication skills - Ability to deal with ambiguity and priority setting in a fast-paced environment Proven understanding of day-to-day business activities, reporting and operations Computer literacy. Proficient in MS Office. Knowledge of SAP and retained samples when running low. Strong work ethic and good attendance. Work effectively with other associates. Work effectively under pressure. Follow EHS policies and procedures. Flexible shifts / hours. Interact with other Site Departments (Production, Planning, Inventory Control, Logistics, Customer Service) KEY COMPETENCIES Analytical thinker, decision maker, experienced in problem solving and troubleshooting. Team player - Diligent, proactive, observant, detailed, organized, and willing to learn. Starting rate for Quality Control Technician is $35.00/hr. plus $2.00/hr. shift differential for hours worked from 2:00pm-6:00am. The compensation range reflects the Company's reasonable expectation at the time of posting. We consider a number of business-related factors when making individual compensation decisions including, but not limited to, education, experience and training. Step progression available based on qualification - minimum of 12 months prior to associate qualifying. Huntsman is proud to be an equal opportunity workplace and is an affirmative action employer. We provide equal employment opportunities (EEO) to all qualified applicants for employment, without regard to race, color, religion, sex, national origin, disability status, protected veteran status, gender identification, sexual orientation and/or expression or any other characteristic protected by law in every location in which we have facilities national or local. Please refer to ****************************************************** for Company's Data Privacy and Protection information. All unsolicited resumes presented by recruitment agencies are treated as pro bono information or service. Huntsman is aware of a scam involving fraudulent job offers. Huntsman does not make job offers until after a candidate has submitted a job application and has participated in a face-to-face interview. Please be advised that emails from Huntsman always end in “@huntsman.com” , and that any job offer that requires payment or requires you to deposit a check is likely a scam. If you have questions about any open positions at Huntsman, please visit our Careers website at ******************************************** Additional Locations:

Job Details 0T534 CA - El Monte, CA Full Time $29.22 - $35.20 Hourly 2nd ShiftDescription Who we are: The Gill Corporation is one of the world's largest manufacturers of honeycomb, high performance floor panels, cargo compartment liners and original equipment for passenger and freighter aircraft. The company also excels in many other types of reinforced plastics including interior sandwich panels for creating structures such as aircraft galleys and bulkheads, honeycomb core and related products. Summary: The CMM Quality Inspector by using the Gill Process Documents (i.e.: GPS, GMS, GOS), performs essential duties to meet customer and AS9100 requirements and supports engineers with complex tasks. This position also works on quality-related projects with direction from the Quality Control Manager. Essential Duties and Responsibilities include the following. Other duties may be assigned. Follow company policies and procedures Comprehend and ensure compliance with internal quality documents, and customer specifications Read and understand customer specifications, process standards, drawings (blue prints), ANSI procedures, and industry standards. Coordinate with CNC production to inspect and rework parts in a timely matter. Must be able to setup, program, and operate Coordinate Measuring Machines, both traditional in-place and articulated-arm (Romer) devices. Proficient in reading blueprints, understanding GD&T, and working with associated technical documents. Proficient in the selection of appropriate hand-held and/or surface plate measuring equipment appropriate to the task. Comfortable providing instruction for the development of Inspection employees within the organization. Qualifications 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. Qualifications and Education (Required) Functionally capable in the use of Microsoft Office and other basic computer software. Ability to comfortably multitask with minimal supervision. Ability to effectively communicate verbally and in writing Acceptable Vision Test results Hexagon Metrology coordinate measuring machine level 1 Working knowledge of PC-DMIS software ITAR Requirement: This position requires access to information that is subject to compliance with the International Traffic Arms Regulations (“ITAR”) and/or the Export Administration Regulations (“EAR”). In order to comply with the requirements of the ITAR and/or the EAR, applicants will be asked to provide specific documentation to verify U.S. person status under the ITAR and the EAR. A “U.S. person” according to their definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee, or asylee. The Gill Corporation is an Equal Opportunity Employer . Applicants for all job openings are welcome and will be considered without regard to race, religious creed, color, age, sex, gender identity, gender expression, genetic information, sexual orientation, national origin, religion, marital status, medical condition, physical or mental disability, military service, veteran status, pregnancy, childbirth and related medical conditions, or any other classification protected by federal, state, and local laws and ordinances. The Gill Corporation provides reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disability Act and applicable state and local law. If you require an accommodation in the application process, please notify the Human Resources Department

At Ensign-Bickford Aerospace & Defense Company (EBAD), we believe that our strengths are built on our most important resource - our people. Join EBAD and you'll be a part of a team who creates cutting edge technology that will blast us into the future. No other company can match the innovative energetic solutions that we provide. At EBAD you will actively contribute to successful missions putting men, women and satellites into space, and protecting our armed service men and women around the world. If this is the culture and work environment you are seeking, then EBAD is the place for you! Job Description EBAD seeks a Quality Control Technician, located in our Moorpark, CA facility. Responsibilities: The candidate will be responsible for providing effective verification of products and certification packages against requirements and the communication of findings associated to the verification. Perform inspection of components and assemblies as part of receiving inspection Maintain accurate, neat and complete inspection records Keep work area organized and clean and follow all established safety guidelines Work within a team structure to achieve company and department goals Perform additional duties related to specific area assignments when requested Requirements: The successful candidate must have graduated from High School or equivalent G.E.D. and 5+ years of experience with inspection of mechanical components in an aerospace or defense related company. Required experience includes Capable of utilizing all standard inspection tools and equipment including calipers, micrometers, drop indicators, CMM and optical systems Must be capable of programming a CMM. The ability to operate and program a Mitutoyo Vision CMM, QV Pak Software, is highly desirable. Knowledge of ISO/AS procedures Must be able to read and interpret Geometric Dimension and Tolerance (GD&T) Must be able to read and understand military specifications and industry standards Read and understand English Effectively communicate and interact with all levels of management High attention to detail Basic PC fundamentals, knowledge of Microsoft Office is essential. Desired skills: Six Sigma Green Belt through ASQ, CQE/CQM Certification program is a plus. Significant experience working directly with internal/external customers and suppliers. Compensation: Salary Range: $50,000 - $80,000 per year. Salary is determined by the applicant's education, experience, knowledge, skills, abilities, internal equity, and alignment with market data. Ensign-Bickford Aerospace & Defense Company is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to race, religion, color, sex, age, disability, sexual orientation, genetic information, national origin, or veteran status.

Shift: graveyard/night shift (11pm start) Compensation: $21-31/hr To support our Digital Cinema department, we are seeking a swing-shift QC Technician who can fulfill the responsibility of linear QC for Digital Cinema Package (DCP) in a theatrical and/or production suite environment, while ensuring that all security protocols are followed when dealing with sensitive material. The ideal candidate will have a good understanding of DCP including image, audio, accessibility and immersive elements. They should have knowledge and experience with Digital Cinema playback servers, audio, captioning, motion devices and other equipment required to carry out the QC workflows. In addition, QC experience with other formats and media including IMP, video, discs are pluses. They should be highly motivated, possess a flexible attitude, keen eye for details and a highly effective communicator especially with clients. They should also able to work as part of a team that deals with changing priorities and workloads. Responsibilities: * Perform theatrical QC services * Perform QC on other materials such as sources from clients (for example DCDM, DSM, video, audio on workstations such as DVS Clipster, Resolve, Colorfront's Transkoder etc) * Perform the above QC internally or/and with clients * Manage client engagements in the theaters where appropriate * Ingest materials via physical media or electronic transmission to playback servers or devices such as Dolby IMS2000, GDC, Doremi etc * Create detailed QC reports * Follow internal as well as client specific security protocols * Must be willing to work weekends, holidays and past their normal scheduled shift if needed * Create stereography maps for foreign language versioning * Other related tasks as assigned to fulfill responsibilities

Qualifications: The Quality Specialist plays a critical role in ensuring product integrity and compliance by conducting standardized testing and analysis on raw materials, in-process items, and finished goods. This position supports the broader Quality Department by maintaining accurate records, calibrating lab equipment, and contributing to continuous improvement initiatives. The role requires strong attention to detail, proficiency in SAP, and adherence to safety and documentation protocols, while also collaborating with cross-functional teams to uphold quality standards throughout the production process. Minimum associate degree in chemistry or equivalent college credit or 3 years minimum technical/lab experience. Experience in Quality Control preferred. Background in materials testing - viscosity testing, melting point testing and general lab testing. Knowledgeable in the use of laboratory equipment and instruments. Good communication skills - verbal and written. Able to work well in a team environment. Computer literate -MS Office Responsibilities Perform standard quality control testing on incoming raw materials, semi-finished goods, and finished goods according to specifications. Accurately calculate and report test results. Able to locate needed test methods, SOPs, and work instructions in the document management system. Record test data into the SAP database. File and maintain the retain samples;dispose of old retain samples per retention protocols. Maintain clean working environment including lab benches, retain sample room, ovens and hood. Participate in Quality Lab 5S activities. Actively participate in daily Quality Lab / department (MOS) meetings. Complete, maintain and control the required Quality records and/or documents as directed by the department standard operating procedures. Use proper Good Documentation Practices (GDPs) when recording information. Perform and support validation and calibration of lab equipment including documenting and reporting equipment issues within the lab. Assist Quality Engineers with complaint investigations and testing samples/reports. Comply with all Health, Safety and Environmental rules, procedures and regulations. Support training efforts within the lab and maintain status for all learned test methods and requirements. Proficient in SAP about Quality Lab transactions. Also including all responsibilities entailing the upkeep of the Quality Department and any assigned projects determined by departmental Manager, Supervisor, and Leads.

Ruggable is a leading direct-to-consumer e-commerce brand based in Los Angeles, California with an extraordinary track record of high, profitable growth. We pride ourselves on having an extremely loyal customer base and a talented team made up of genuinely caring people who take action and deliver results. We are venture-backed and own a patented washable rug design that's disrupting the home décor industry. Our mission is to empower our customers to live vibrantly with beautiful products that don't compromise on function. If you're passionate about consumer products, e-commerce, and high-growth start-ups, keep reading! Please note, this role is onsite five days a week, Monday through Friday, 7-4 or 8-5 pm. Job Summary: We are seeking a Quality Technician to support our daily manufacturing operations. This role helps ensure every product meets our quality standards by supporting the systems that keep our output consistent for customers. The Quality Technician will work closely with on-site Quality, Production, and Engineering teams to identify issues, assist with corrective actions, and reduce variation in our processes. This position plays a key role in maintaining reliable, repeatable production and ensuring compliance with both customer and internal standards. What You'll Do: Perform routine quality checks, measurements, and visual inspections to ensure products create exceptional experiences for our customers Support on-site manufacturing quality process control activities and maintain accurate documentation Assist in maintaining quality records, equipment logs, and inspection documentation to support consistent production and compliance Work directly with local Production, QA, and Engineering teams to provide data and observations during root cause analysis (RCA/CAPA) efforts Monitor visual and dimensional product characteristics, especially color consistency, and promptly communicate discrepancies to supervisors Collect, organize, and report quality and process data for trend analysis and continuous improvement What You'll Need to Have: Required: Associate degree in a technical field or equivalent hands-on experience in quality 0-1 years of experience in a production, quality, or manufacturing support role Working knowledge of basic quality tools (control charts, check sheets, 5 Whys, basic FMEA concepts) Ability to perform accurate measurements, visual inspections, and data collection Proficiency with Google Sheets/Excel and basic data analysis techniques Strong attention to detail, communication, and teamwork skills Comfortable working in a fast-paced manufacturing environment Preferred: Experience with visually critical characteristics such as color consistency Exposure to quality audits, feedback loops, or process verification activities Familiarity with ISO standards or retail/consumer product compliance Experience in wholesale, retail, or direct-to-consumer manufacturing environments' Compensation: $69,000-80,000 annual salary range (depending on location and experience) An annual bonus percentage that varies based on level of role Employer matching (up to 3% of base salary) for company sponsored 401k plan At Ruggable, we offer competitive compensation and benefits packages. Ruggable is an Equal Employment Opportunity employer. We proudly recruit and hire a diverse workforce and are committed to creating an inclusive environment for all employees. If you are based in California, we encourage you to read this important information for California residents linked here. To all recruitment agencies: Ruggable does not accept unsolicited agency resumes. Please do not forward resumes to our jobs alias, Ruggable employees or any other company destination. Ruggable is not responsible for any fees related to unsolicited resumes.

工作内容： W.H.P.M., Inc., established in 1993, is a privately held corporation headquartered at Irwindale, California, only 15 minutes away from downtown Los Angeles. The Company is a pioneer in the research and development of one-step rapid membrane tests. It has been designated a registered GMP facility for in vitro diagnostic medical devices by the FDA. Responsibilities *Ensure all raw materials and finished products are compliant with documented specifications and procedures though testing. *Works closely with Quality Assurance and Production personnel to ensure a quality product is being assembled as per documented procedures. *Accountable for the inspection, testing, and release of all raw materials, in-process materials, and testing of all finished products per documented specifications and procedures. *Accountable for release testing for all shipments. *Work with Management to improve product quality and assembly execution. *File daily paperwork and assist in maintaining all quality records. *Assist with recording and testing of customer complaints. *Promote and maintain a safe work environment while practicing safe work habits and procedures. *Other duties as assigned. Mandarin Speaking Required 工作条件： 可以合法报税,工作氛围融洽,需具有责任心,细心,有团队合作精神 工作时间： 周一至周五8小时,法定节假日休息 职位为全职工

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Title responsibilities include, but are not limited to, the following: Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in a clear, accurate, technically proficient manner Qualifications The ideal candidate would possess: Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Additional Information Location: Burbank, California Employment Type: Part-Time Schedule: Day Shift Salary: $20.00-22.00 Per Hour

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Title responsibilities include, but are not limited to, the following : Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in English - in a clear, accurate, technically proficient manner Qualifications The ideal candidate would possess: Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Basic Minimum Qualifications : Native Japanese speaker Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Location: Burbank, California Employment Type: Part-Time Schedule: Day Shift Salary: $20.00-22.00 Per Hour

Job DescriptionDescription: The Quality Control is responsible for overseeing and managing all aspects of quality control processes within the organization. This role involves leading a team of quality control inspectors, implementing quality standards, and ensuring compliance with industry regulations. The ideal candidate will have strong leadership skills, attention to detail, and a deep understanding of quality control practices, particularly in GMPs (Good Manufacturing Practices) and HACCP (Hazard Analysis and Critical Control Points). What We Offer: Comprehensive Medical, Dental, and Vision Insurance Enjoy discounts on organic meals daily Opportunities for career growth Key Responsibilities: team of quality control inspectors. Assign tasks and responsibilities to team members and ensure the timely completion of quality control activities. Conduct regular performance evaluations and provide feedback to team members. Develop, implement, and maintain quality control procedures and standards in compliance with GMPs and HACCP. Oversee the inspection and testing of products to ensure they meet quality specifications. Analyze quality data and identify trends or areas for improvement. Ensure compliance with industry regulations and company policies. Maintain accurate records of quality control activities, inspections, and test results. Prepare and present reports on quality performance and improvement initiatives. Identify opportunities for process improvements and lead quality improvement projects. Collaborate with cross-functional teams to address quality issues and implement corrective actions. Stay updated with industry trends and advancements in quality control techniques, particularly GMPs and HACCP. Develop and deliver training programs for quality control staff. Ensure all team members are knowledgeable about quality standards and procedures, with a strong focus on GMPs and HACCP. Requirements: Qualifications: Minimum of 5 years of experience in quality control or quality assurance, with at least 2 years in a supervisory or lead role. Experience in the [specific industry] is preferred. Knowledge: In-depth knowledge of Good Manufacturing Practices (GMPs) and Hazard Analysis and Critical Control Points (HACCP) standards. Skills: Strong leadership and team management skills. Excellent analytical and problem-solving abilities. Proficiency in quality control software and tools. Strong communication and interpersonal skills. Physical Requirements: Ability to lift up to 35 pounds. Ability to stand for extended periods and perform repetitive tasks. Comfortable working in a manufacturing or production environment. Benefits: Competitive salary and performance-based bonuses. Health, dental, and vision insurance. Professional development opportunities.

Responsible for monitoring the quality of perishable products in the warehouse on an ongoing basis, inputting orders through data entry while performing extensive customer service duties, and performing other related duties as required. Regularly exercises discretion and independent judgment in performing duties directly related to the general operation of produce quality control. RESPONSIBILITIES: Check produce in slots on a daily basis to make certain product that is set up for shipping is up to acceptable standards Communicate with buyers all quality issues and assists them in resolving them to ensure the customer receives the highest quality products possible Ensure products are being rotated properly during daily slot checking, and communicate any problems with rotation to the stockers and/or supervisors responsible Monitor variance reports for accurate accounting of spoilage, warehouse damage, truck damage, etc. Greet all internal and external customers in a friendly and efficient manner in order to ensure that proper customer service is maintained and customer satisfaction and organizational efficiency are enhanced Inspect in-bound freight, warehoused product, and/or outbound product and document product condition Communicate regularly with necessary parties on the company's status on product quality Analyze, identify, and propose action to the solution of problems associated with Quality Assurance Observe all safety rules, regulations, and sanitation policies Salary Range: $24 to $30

TempToFT Perform inspection and CCP/preventative controls checkups on in process products ? Perform daily operation checkups of product and in process materials, including but not limited to review for completeness, label check, weight check, Lot codes, Allergens and visual inspection of products ? Identify and control non-conforming materials/products and equipment ? Formula/recipe verification and traceability checks for raw materials ? Perform all quality control checks, including but not limited to: inspecting the lines during pre-operational time periods; taking in-process or finished product samples for analytical or microbial testing; Sampling components, and recording accurate information on all required forms. ? Address any questions and concerns on food safety and quality control/assurance with QA management in a timely manner ? Allergen and ATP swab/checks equipment for approval, pre-operational and operationals inspections ? Performs calibration and preventive maintenance (as applicable) on analytical testing equipment both in the laboratory and in production as required. ? Assist in training plant operators in quality test procedures. ? Participate in plant self-inspections auditing of Good Manufacturing Practices. ? Testing and documentation for raw materials acceptance. ? Perform checks for all the pre-requisite programs (i.e., Food defense, Allergens, Sanitation, Glass and brittle plastic, etc.) ? Other duties and projects as assigned.

Temp 1. Provide training and guidance to employees who lack knowledge or are unable to practice 2. Maintain documentation and procedures in accordance with the standards of the relevant agencies --------------------------------------------------------- Description Company is one of the fastest-growing chain of retail stores and supermarkets offering the widest selection of Japanese and Hawaiian imported grocery and retail products in the nation. Due to the expansion of our business, we will be opening a new central kitchen in Torrance this fall. We are looking for employees to join our Delicatessen, Sushi, Fresh Fish, Meat, Data Entry, Receiving, and QC departments. The QC/Health associate is responsible for performing a variety of duties from verification record to receiving desk vender service. The QC/Health associate often is responsible for running safety records, completing HACCP records for maintain safe environment. S/he must be detail oriented and good with numbers. ESSENTIAL Inspects incoming and outgoing shipments for quality and condition. Creates a quality inspection report for all inbound ingredient. Conducts regular product inspection in all coolers and refrigerated warehouse space to ensure quality and proper rotation of products. Conducts random shipping audits for outbound product quality and condition. Performs with inspecting Production packing quality of products. Performs with shelf life testing. All other duties as assigned and/or required. NON-ESSENTIAL • Maintains high ethical standards in the work place. • Provide assistance to understaffed departments. • Complies and maintains confidentiality of all company policies and procedures.

We are seeking a Quality Control (QC) Inspector to join our team in Santa Fe Springs, CA. This is a Temp-to-Hire position, offering an excellent opportunity to grow within a fast-paced, quality-driven environment. As a QC Inspector, you will be responsible for ensuring that materials, processes, and products meet the highest standards of quality. Key Responsibilities: Perform regular inspections of materials using measurement equipment such as micrometers, calipers, and rulers. Ensure work packets are complete, accurate, and GDP compliant; make corrections as needed. Conduct mathematical calculations required to assist in completing inspections. Maintain a high standard of quality control methodologies and inspection techniques. Work closely with the QC Department and Production teams to resolve any issues and improve processes. Qualifications: Experience: Minimum of 2 years of QC experience, with at least 1 year of experience in the Medical Device, Pharmaceutical, or Aerospace industry. Skills: Proficiency with micrometers, calipers, and other measuring equipment. Certifications: HS Diploma or equivalent; knowledge of ISO 13485 and 17025 standards is a plus (but not a requirement). Independence: Ability to work independently with minimal supervision. Attention to Detail: Strong ability to catch discrepancies and ensure compliance with industry standards. What We Look for in a Candidate: Independent worker with the ability to solve problems autonomously. Strong communication skills, both written and verbal. Team-oriented with the ability to collaborate effectively with internal departments. A keen eye for detail and a passion for quality. A proactive, assertive individual who can handle high-stress situations without compromising on quality.