Quality Control Technician jobs in South Whittier, CA

Quality Inspector - Medical Device (QA & Inspection Focus) 📍 Onsite - Irvine, CA 💰 $21 - $27/hour 🕕 Shift: 6:00 AM - 2:30 PM (May shift to 7:00 AM - 3:30 PM) 📅 Contract: 6-Month Contract with Possible Extension 🔑 Key Responsibilities Perform receiving and in-process inspections Interpret blueprints, GD&T, and complete First Article Inspections (FAIs) Use inspection tools: hand tools and Keyence measurement system Identify and distinguish critical vs. non-critical dimensions Understand and apply dimensional tolerances down to the thousandths Conduct label inspections, document reviews, and issue Certificates of Conformance (COCs) Ensure compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) Provide feedback on GDP corrections to site personnel Follow established quality procedures and contribute to continuous improvement Accurately document and report nonconformances in the QMS ✅ Requirements Minimum 2 years of QA or Inspection experience in a regulated environment GMP and GDP experience required Medical device experience is a plus Strong understanding of inspection tools, measuring systems (Keyence), and procedures Proficient in English reading, writing, and verbal communication High attention to detail and ability to follow written procedures Comfortable working independently and as part of a team Basic computer skills and familiarity with manufacturing software High school diploma or equivalent preferred 📩 Apply now if you're ready to contribute to a high-quality, fast-paced environment with a focus on precision and compliance. 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.

is a 6-month contract to HIRE paying around $23-$25/hr. 2 years of QC experience specifically in a production line (In-Line) Medical Device experience Strong computer skills Strong knowledge of NCR (non-conformance reports) Detail-oriented Nice to Have Skills & Experience Receiving inspection experience ERP experience Job Description Insight Global is looking for a Quality Control Inspector for a medical device client in the Irvine, CA area. They will be responsible for in-line inspections, both top assemblies and finished goods. This position is for 1st shift (7am-3:30pm, Monday-Friday). They will then learn and be a part of receiving inspections once comfortable with training.

This position offers an exciting opportunity to work in a dynamic, fast-paced environment while playing a critical role in the microbiological testing and quality control process. If you meet the qualifications and are looking for a challenging and rewarding career, we encourage you to apply. Location: Chino, CA Pay: $24-28/hr Shift: Monday-Friday 8-5pm. Contract, with opportunity to extend or convert. Key Responsibilities: Perform microbiological testing on bulk samples, finished goods, raw materials, and other samples as outlined in SOPs. Conduct preservative efficiency/challenge testing as needed. Review, interpret, and execute test protocols in accordance with established procedures. Develop and coordinate document control systems related to microbiological testing. Maintain and coordinate the calibration of equipment to support compliance with Quality Control (QC) standards. Maintain various departmental logbooks to document test results and other relevant data. Provide clerical support to the department by typing memos, reports, and spreadsheets, and assisting with filing and distribution. Handle communication through emails, phone calls, and faxes as required. Understand and adhere to all Good Manufacturing Practices (GMP) and safety protocols in the work environment. Utilize appropriate personal protective equipment (PPE) such as gloves and safety glasses when necessary. Provide support to other areas of QC with clerical assistance as needed. Perform other duties as assigned by management. Qualifications: Bachelor's Degree in Microbiology or a related field, or at least two years of coursework and laboratory experience in Microbiology. Knowledge of microbiological methodologies and practices. Excellent written and verbal communication skills in English. Proficient in statistical and mathematical analysis. Strong problem-solving, decision-making, and organizational skills. Knowledge of Microsoft Office and other computer applications. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Job Description Electronic lab technician ($24.00 to $40.00 per hour) The Staco Story For more than 60 years, the biggest names in aerospace and defense have trusted Staco Systems as the provider of choice for critical cockpit control systems. While competitors have come and gone, Staco is still going strong, propelled by superior engineering and continual technology development, including unique advances in optics, weight reduction and miniaturization. This technical superiority has led the company to continually enhance its standard offerings with unique custom solutions engineered and built to solve a customer problem or meet a customer specification. The company was founded in Costa Mesa, California in 1958, serving the many aviation and defense companies based in southern California. Today, our sales representatives are located in over 35 countries. Selling to the most demanding industries military, aerospace, shipboard, and precision industries Staco Systems expansion is due to a commitment to quality in creating custom solutions for its customers. Our products have been certified with numerous standards boards, military and supplier certifications including AS9100 and MIL-SPEC. Originally known as Staco Switch, the company began by offering lighted pushbutton display switches including the first Series 30 switch, which was used in a Fokker F-27 in 1960. We remain one of the world's preeminent providers of these products. The Staco Systems product suite is continually expanding, and now includes rugged keyboards and keypads, electronic controllers, panel assemblies and edge-lit panels. Staco Systems headquarters is in Irvine, California with international sales offices in Europe. Job Summary The electronic lab technician will work in an engineering environment building and testing prototype electronic and electromechanical assemblies. The electronic lab technician will also assist in the troubleshooting and diagnosis of manufacturing defects and report their findings to the appropriate engineering personnel. The electronic lab technician will be expected to work with minimal supervision and manage their workload as required. The electronic lab technician will also support qualification testing of new and existing products which may require travel to outside testing facilities. Receives Direction From: VP of Engineering Provides Direction to: No direct reports Examples of Essential Functions: Responsibilities include, but are not limited to, the following: Building and debugging of prototype PCB assemblies Building and debugging manufacturing test jigs and fixtures. Work with team to analyze product return RMAs down to component level Be able to collect data, interpret trends and present it to management Knowledge of electronics (Ohms Law, Read Schematics, DPDT Switching), required Must be proficient and understand the accuracy limitations in the use of electronic test equipment (DVM, Dielectric Tester, Power Supplies, Oscilloscopes, Soldering) Must have excellent written and verbal communication skills Qualifications Guidelines Education/training/experience: An Associate's degree in Engineering or equivalent experience is desired 4 or more years working in an engineering lab environment Must have experience working with surface mount PCBAs Must have experience working with microcontrollers and firmware Must have experience working with electro-mechanical products Must be able to read and understand engineering drawings and schematics Must be proficient in Microsoft Office Suite Knowledge of: The primary duties of this position involve the performance of work requiring advanced knowledge in the field of electronics acquired by a prolonged course of specialized intellectual instruction. With this advanced knowledge the person in this position must be able to analyze, interpret, or make deductions from varying facts, data or circumstances and exercise discretion and judgment. Physical Standards: Ability to move throughout plant as required Ability to sit and operate a computer workstation and microscope Good eyesight and finger dexterity Works well with all levels of employees May be occasionally required to lift up to 25 pounds and rarely up to 50 pounds Reasonable accommodations will be considered that would allow the employee to perform the essential functions of this job Job Posted by ApplicantPro

Job DescriptionDescription: Job Title: QC Sr. Chemist Department: Quality Control Reports To: Manager, QC FLSA Status: Exempt Summary: The QC Sr. Chemist will be involved in multiple on-going projects and will serve in a cross-functional role. Activities include performing analysis in a GMP/GLP environment for release testing, supporting manufacturing functions (engineering, validation, etc.), stability studies, method validation and transfer in a SDMS environment. This individual will lead raw material, intermediates, and finished products release in QC laboratory. The individual should have good communication and organizational skills and be able to coordinate work with cross-functional team members, peers, and external Laboratories and CMOs (Contract Manufacturing Organizations). The Sr. Chemist will serve as a mentor/trainer to Chemist. Essential Duties and Responsibilities: Perform testing using analytical equipment (HPLC-MS, HPTLC-MS, GC-MS, IR, UV, TOC, etc.) as well as using traditional wet chemistry methods (i.e. titration, TLC, etc.) Serve as in-house Subject Matter Expert on Instrument operation, including but not limited to HPLC, GC, HPTLC, FTIR, etc. Work under minimal to no supervision. Participate in Technical Transfer and method development activities with the Scientist, validation personnel and/or contract labs. Perform analytical method transfer, and validation as directed from provided protocols. Investigate deviations and write exception/ OOS/OOT documents. Own/follow up on CAPAs. Author, revise and review documents and reports including but not limited to SOPs, test methods, safety assessments, trend reports, qualification/validation summary reports, technical reports, method assessments, technical assessments, microorganism assessments. Process and interpret chromatographic data independently and communicate significance of results to management, while maintaining Data Integrity standards. Enter experimental information into lab notebooks and process analytical data accordingly. Coordinate with team members to ensure seamless analytical coverage during manufacturing campaigns and on-going stability studies. Coordinate with team members to verify each other’s data by reviewing in a timely manner. Take personal responsibility to meet analytical testing and data verification deadlines. Review analytical data for accuracy and release/reject results. Maintain documentation, equipment and work area in orderly condition at all times. Initiate/facilitate improvement projects to drive efficiency of the laboratory performance. Serve as mentor/trainer to Chemist and Laboratory Coordinator. Facilitate/ initiate projects that may improve laboratory compliance and laboratory output. Participate in audits. Proactively and cooperatively connect with peers and management to ensure awareness of progress and issues; recommend solutions when issues arise. May be required to perform other duties as assigned or as needed. Supervisory Responsibilities: This position has no supervisory responsibilities. Requirements: 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. Education and/or Experience: Must have a Bachelor’s degree in Chemistry or related science with 6 + years’ experience in a regulated industry (i.e. pharmaceutical, dietary supplement, biotech, etc.); or equivalent combination of education, training and/or experience. 4 + years of experience with USP/AOAC is required. Experience with analytical method verification, development, validation or transfer, is required. Experience in operating, maintaining, and troubleshooting instruments is required. Experience using analytical instrumentation including analytical balances, TOC, spectrophotometers, etc. is required. Experience working in a regulated (i.e. FDA, NPA, etc) GMP environment is required. Experience in maintaining data integrity is required. Hands-on experience with chromatography equipment is required. Experience with EP, BP, ACS, and ICH guidelines is preferred. Experience with SDMS/LIMS computer system validation and reviewing data, and audit trails in Part 11 compliance systems is required. Experience with LCMSMS, GCMSMS, ICP-MS, qPCR Microbiological analysis and UHPLC/HPLC equipment with Empower 3 Chromatography Software is preferred. Experience with preventive maintenance and calibration of instruments is preferred. Knowledge, Skills and Abilities: Good understanding and in-depth knowledge of cGMP, SOP's, GLP, QA/QC is required. Good communication skills both oral and written. High energy, self-motivated individual who is detail focused, organized, and able to multi-task between multiple active projects. Ability to work under pressure and perform tasks on schedule with minimal supervision. Able and willing to work in a team environment and participate in cross functional team activities. Able to troubleshoot instruments when needed. Make discretionary decisions on regular basis. Demonstrates strong organizational and time management skills. Ability to work with others and independently. Ability to write routine reports and correspondence. Must demonstrate effectiveness in ability to train others, empowerment, leadership, results orientation, and task completion. Competency to properly gown for and function within a GMP environment. Discipline to consistently follow SOPs, GMPs, and safety precautions. Strong analytical reasoning skills & excellent written and verbal communication skills. Knowledgeable in Microsoft Office, Outlook, and similar programs. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms. The employee is frequently required to stand; walk and talk or hear. The employee must regularly lift and/or move up to 10 pounds, occasionally lift and/or move up to 25 pounds. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate.

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) The salary range for this role is: $20 - $29 AeroVironment considers several factors when extending an offer, including but not limited to, the location, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. 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 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

Job Description The Document Control Associate manages quality documentation, processes and records at Critical Innovations, applying best practices from within the field of quality control to ensure that the Quality Management System remains effective and up-to-date. The Document Control Associate will assist in the management and implementation of the Quality Management System to ensure compliance with ISO 13485, the FDA's Quality System Regulations 21 CFR Part 820, including compliance with FDA Regulatory requirements for combination products that are either device- or drug-led (CDRH or CDER) encompassing cGMP for pharmaceutical products 21CFR Parts 210 and 211. The Document Control Associate will provide additional support to the Quality Management System's activities as assigned at the discretion of management. This is an on-site, full-time position. Reports to: Vice President of Quality Assurance & Regulatory Affairs. Duties and Responsibilities: The Document Control Associate's responsibilities typically involve: Performing and documenting work in compliance with ISO 13485, the FDA's Quality System Regulations and cGMP. Assisting with implementing and maintaining a quality system that is compliant with ISO 13485 and the FDA's Quality System Regulation requirements. Assisting with management of Document Control, Document Change Orders, Quality Records and Design History Files. Maintain Quality System documents and records (hard copy and electronic format). Management of Document Change Orders for approval, release and implementation, including notification of external vendors where appropriate. Review Document Change Orders for accuracy and completeness. Format documents submitted for Document Change Orders (revision or original release). Management of Document History Records. Management of Quality Document Logs. Coordinate destruction of expired records and documents. Ensure that controlled copies of latest approved Quality documents are managed, updated and available at points of use. Assist Project Managers with update of Design History Files. Assist with formal audits through retrieval and provision of requested documents in a timely manner and assist with completion of audit reports. Commonly exercise decision-making and discretion in performing job-related tasks. Additional support for the Quality Management System activities as assigned. On a daily basis, assess overall workload for any area that needs help, and assist coworkers and provide backup as needed without being reassigned by management. Skills and Experience: Excellent communication both written and orally. Excellent problem-solving and critical-thinking skills. Excellent attention to detail. Ability to work independently with ability to complete routine tasks with little or no supervision. Ability to work in a cross-functional team environment. Ability to edit and proof documents. Experience of ISO 13485 Quality Management Systems. Experience of FDA's regulations and cGMP as it pertains to Document Control. Proficient with Microsoft Office Suite. Self-motivated with strong time-management skills and capable of working with minimal supervision. Highly organized and detailed oriented. Able to perform light to moderate lifting and ability to sit at a computer for terminal for an extended period of time. Education and Training: Required: Bachelor's degree (BA/BS), and/or One year or more experience in a Quality Assurance/Document Control role in the Medical Device, cGMP-regulated Pharmaceutical environment or related field is preferred. Working knowledge of the FDA's QSR 21 CFR Part 820, ISO 13485 and cGMP as it pertains to document control. Authorization to work in the United States indefinitely without restriction or sponsorship. Critical Innovations is an Affirmative Action/Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veterans' status, or any other characteristic protected by law. To conform to U.S. Government Department of Defense regulations, you 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. Benefits: 401(k) Safe Harbor Plan Healthcare Insurance: Medical, Dental and Vision Other Insurance: Life Insurance and Long-Term Disability (LTD) Insurance Time Off: Paid Time Off (PTO), Paid Sick Leave, Paid Holidays, and Paid Bereavement Leave Tuition Reimbursement Program Performance Bonus Flexible Schedule Lunches, Snacks, Events Schedule: Monday to Friday Salary $55,000 - $75,000 per year Privacy Policy | Critical Innovations

Job Description Swift Engineering Inc ************************ is uniquely positioned in the marketplace to provide both Product Development and Manufacturing products and services, specializing in advanced composites, unmanned systems, robotics and associated technologies. Description: Engineering Technician(s) will be working closely with engineer(s), program manager(s), manufacturing (mfg) engineering manager, and other mfg. team members to manufacture and assemble composite/metallic products and vehicles for Swift. Pay Range: $71,000 to $93,000 Annually FLSA Status: Non-Exempt (hourly) Reports to: Manufacturing Manager Duties and Responsibilities: Develop, refine, and recommend lamination, drilling/finishing, and assembly processes for prototype or LRIP programs Prove/verify new processes or procedures and provide feedback to management to improve process Assist Operations personnel in clarification of technical or ambiguous requirements Assist in tool design / MFG aids Assist or perform in critical process including, but not limited to: Composite/composite or composite/metal or metal/metal bond/liquid shim operations Laminate complex components using different composite materials Trim and drill components for assembly Installation and in-process quality control of aerospace fasteners Composite/metallic repair Assemble sub-assemblies and integrate onto main assembly Assist in operation of sensitive equipment including, but not limited to: Application of strain gages Hydraulic proof loading and/or test to failure rigs Environmental test chambers Autoclave operation, maintenance, and troubleshooting Assist in shop floor supervision and resource scheduling Under standard supervision, applying trained procedures and collaborative solutions to meet work requirements. Priorities are determined by management. Support and comply with all quality standards and management systems (Swift Internal, NADCAP & AS9100) Elevate issues to management Maintain a neat and orderly work area (e.g. general shop floor, clean room, trimming area) Comply with all Company policies, procedures and regulations Requirements Qualifications: Requires at least 5 years of experience in an aviation related technician field Requires an Associate’s degree in engineering or related experience. If no Associates degree has been earned candidate must have at least 7 years of experience. Knowledge and experience using various hand tools associated with assembly work Drilling/trimming Techniques – both free-hand and with drilling/routing fixture Measuring – use of precision measuring devices such as calipers, gages, indicators, micrometers, etc. Aerospace fastener/cleco specialty installation equipment and QC tools Knowledge and experience handling composite materials (core, pre-impregnated composite, wet-lay, etc…) Knowledge and experience preparing lamination molds/tools using chemicals and hand tools such as sealer, release, scriber, etc Knowledge and experience working with aerospace adhesives and resins, which includes but not limited to bond prepping, adhesive/resin mixing, adhesive application, dry fitting, liquid-shimming, wet-bonding with fasteners and/or cleco’s Knowledge and experience doing body work on irregular surfaces, including using filler materials, scuff sanding, applying primer and touch up paint as required. Knowledge and experience repairing metallic or composite aerostructures Knowledge and experience in reading and interpreting work instructions, specifications sketches, job travelers, planning documents and engineering drawings. Teamwork: Work with other people in cooperation and as a good team member. Candidates must be US Person for compliance with ITAR (International Traffic in Arms Regulations). Required Skills: Must be meticulous to ensure quality of work across all products manufactured at Swift Must have strong mechanical aptitude in mechanical assemblies. Industries such as marine, automotive, motorsport, aviation, aerospace and energy are relevant fields of experience Speak, listen and write in a clear, thorough and timely manner Take responsibility for workmanship and productivity Expertise in operating pneumatic tools for trimming, drilling and bonding of hardware, and technical devices for measurement Must be capable of satisfactorily completing all the essential functions as determined by supervisor Preferred Skills: Assist in training and proficient in operation of metrology; Operate Laser Tracker Operate FARO Arms CMM Working Conditions: While performing the duties of this job, the employee is regularly required to stand and talk or hear. The employee is occasionally required to sit; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance and stoop, kneel, bend, crouch, or crawl. The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Requires eye-hand coordination and manual dexterity. Requires corrected vision and hearing to normal range. Equipment Operated: Vacuum pumps, heat sources, special hand tools, ladders, stands, mechanical stands, hi-reach lifts. Work Location: Open shop environment, occasionally in warehouse. Protective Equipment Required: Goggles, safety glasses, face shields, ear protection, aprons, gloves, safety harnesses, respirators, breathing equipment. Potential Hazards: Exposure to high intensity noise levels, extreme changes in temperature, airborne substances, materials identified on Material Safety Data Sheets, working on unprotected heights or around moving machinery. Periodic weekend or evening work is expected. Benefits 9/80 Schedule Health Insurance - 100% covered for Employees Vision Insurance - 100% covered for Employees Dental Insurance - 100% covered for Employees Life Insurance - 100% covered by Swift, plus the option to purchase additional life insurance for you and your dependents. 401k with company match Extremely generous company holiday calendar including a holiday hiatus in December, and highly competitive PTO plans. 16 weeks of paid Caregiver & Wellness Leave to care for a family member, bond with your baby, or tend to your own medical condition. Family Planning & Parenting Support: Fertility (eg, IVF, preservation), adoption, and gestational carrier coverage with additional benefits and resources to provide support from planning to parenting.

Job Description The Building People, LLC, has a position open for a full-time Engineering Technician in Garden Grove, CA. The Engineering Technician shall assist provide the customer with technical support and inspection services relating to maintenance, repair, or alteration of buildings, utilities, parking areas, roadways, and other work/projects on both leased and owned properties. Responsibilities/Duties Utilize Facilities Management software to review estimates submitted by contractors for maintenance, repair, construction, and other work to assure conformance with customer requirements. Ensures that proposals are technically sound and in compliance with Army regulations. Performs technical review & evaluation of plans and reports required to be submitted by the contractor including: Preventative Maintenance Plans for building structures, Quality Assurance Plans, as-built drawings, shop drawing submissions, and change order requests. Reviews drawings and specifications developed by A/E firms for adherence to design requirements, code limitations, and civil, structural, architectural, and engineering fundamentals and principles. Prepares cost estimates, technical specifications, preliminary sketches, & scopes of work for the contract purchase of complex repair and construction items, designs, and plans for alterations, remodeling, and repairs to various types of facilities, machinery, and equipment, new construction, and the development of contracts with organizational policies and procedures. To include estimating the cost of manpower and material, estimating length of time the projects will require, determining and analyzing alternatives when appropriate. Prepares contract modifications and design deficiency reports. May be required to make site visits for the purpose of studying conditions/gathering information to be used in preparation of drawings, etc. Other duties as assigned. *This position will not have supervisory responsibilities. Required Experience & Skills 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. Detailed knowledge of methods and techniques of engineering and the construction, application, properties, operation, and limitations of engineering systems, processes, structures, machinery, devices, and materials. Knowledge and experience of HVAC systems, machinery, plumbing/piping, ventilation, fire protection, digging, shoring, lighting, and similar types of equipment and systems. Experience conducting building inspections/facility condition assessments. Must possess practical working knowledge and experience to develop detailed specifications, cost estimates, and project schedules. Must be able to read and interpret drawings and blueprints. Ability to work independently, efficiently, and prioritize effectively in order meet project deliverables and deadlines. Must be flexible and be able to adapt to rapidly changing requirements and timelines. Familiarity with standard CMMS systems, RS Means & various industry estimating tools, Auto-CAD, MicroStation, and Microsoft Suite. Must be able to read and accurately interpret contract documents. Must always be able to communicate effectively and in a professional manner. Physical Demands - The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee may be asked to walk/stand/bend/climb for extended periods. The employee may occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision. May be asked to drive for several hours during the course of site inspections/investigations. Work Environment - The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The employee will normally work in a temperature-controlled office environment, with frequent exposure to electronic office equipment. During visits to areas of operations, may be exposed to extreme cold or hot weather conditions. Is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals, and loud noise. Required Education Bachelor's degree (B. A.) from an accredited college or university and a minimum of three (3) years of experience, or five (5) plus years of related experience and/or training or equivalent combination of education and experience. Certificates, Licenses, Registrations, Clearance: Currently favorable, or eligible for a National Agency Check with Inquiry (NACI) clearance, in accordance with AR 380­67. Valid Driver’s License. EEP, CEM, or Tridium N4 certifications preferred but not required.

Hourly Range: $25.51-$34.62 **All Applicants must comply with ITAR Requirements. US Citizens or Permanent Residents only** Reporting to the Quality Assurance Manager, a Quality Technician I/II is responsible for up to two of the below functions. The Quality Technician I works collaboratively with teams to develop and improve processes for the WMI Integrated Management System. Common Requirements: Obtains a clear understanding of all internal and external requirements relating to applicable QT Participates in internal audits, Kaizen events, Lean improvements, Six Sigma, and 6S projects when required. Assists with customer/3 rd party surveys and audits as required. Carries out other activities as deemed necessary by the Quality Assurance Manager or Director of M&P Calibration Functions: Calibrate all inspection tools, product acceptance templates and product acceptance fixtures Maintain calibration records for all inspection tools, product acceptance templates and fixtures Create Purchase Orders for external calibration service vendors, as required Coordinate on site-calibration with approved calibration service vendors Review and validate supplier calibration certificates Have knowledge of the ERP system in order to properly maintain calibration frequencies and keep track of new, old and obsolete measuring and inspection tools. Reviews and validates purchase orders and contracts per requirements, quality provisions, as well as statutory and regulatory requirements related to calibration Must pass a yearly proficiency test for “daily hardness verification” and “partial indirect verification” per ASTM-E18 Document Control Functions: Assist with assuring Weber Metals' specification library contains the latest published revisions Assist with the distribution of specifications and clauses relating to manufacturing processes, materials, testing, quality systems, etc. for review by technical authority (e.g. heat treat, non-destructive testing, metallurgy, etc.) Follow up on outstanding specification reviews and coordinates with reviewer to assure completion in a timely manner Help maintain access to all necessary customer portals and industry websites necessary to retrieve and verify specification revisions Assist with document updates, and help coordinate document reviews and approvals Help maintain the Master QMS Document Library by: Releasing documents to responsible owners for modification, reviewing modified QMS documents to assure revisions are completed in accordance with company standards, and posting revised documents to the company's intranet Additional Responsibilities: Other duties as assigned. Qualifications: Must be able to comply with ITAR and EAR residency requirements Effective communication skills, including strong listening skills, and oral and written communication. Ability to multitask and provide results in a timely manner as well as adjust plans under changing circumstances. Works independently and meets commitments and established deadlines for assigned responsibilities, work schedule, appointments, and meetings. Makes appropriate decisions based on analysis, sound judgment, and available information. Promotes a team atmosphere and builds harmonious working relationships both within and outside the department. Computer Skills (Word, Outlook, Excel, PowerPoint). Strong organizational skills. Determination to develop and implement solutions to resolve problems. Education/Experience: A minimum of 3 years of experience in Aerospace manufacturing environment. A minimum of 1 year of experience with calibration responsibilities.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will manage the formulation of powdered media. First Shift: 5:00 am-1:30 pm At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Responsibilities: * Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. * Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. * Suggest changes in departmental procedures and processes (SOPs) as needed. * Performs and documents line clearance at the start of each formulation event. * Maintains all required logs and associated documentation. * Assures that all chemicals are stored and labeled properly. * Performs process scale checks on all required equipment including scales and balances. * Keeps work area, utensils, tanks, mills, and equipment clean and organized. * Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. * Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. * Understands and follows procedures to ensure that chemicals are handled properly. * Good understanding of metric system and its conversions. * Follows and actively participates in sustaining the 6S program in the area. * Other duties as requested by Lead or Supervisor. Required Skills/Education: * High School Diploma or equivalent. * Good work history. * Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. * 1-2 years of hands on experience * General education about chemicals and proper handling (college level science preferred). * Working knowledge of metric system. * Good understanding of current Good Manufacturing Practices (cGMPs). * Ability to speak, read, and write English. * Good oral and written communication skills. Salary and Benefits: * For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). * Medical, Dental, Vision * Life Insurance * 401k * Paid Time Off * #LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Full-time Description The Supplier Quality Technician job duties involve supporting quality, business, and other processes in a team-based manufacturing environment. Performs activities in various cross-functional areas, including production planning and control, total quality management, systems, manufacturing, equipment and facilities engineering, material management, and process reengineering. Apply knowledge of SAP and work processes to manage database administration, purchase price variance, invoice discrepancy resolution, vendor registration, credits, and OA support. Requirements DUTIES AND RESPONSIBILITIES Preparing and maintaining quality management documentation Coordinates root cause analysis and corrective action responses to customer complaints, internal product or process nonconformance, and audit findings Completion of internal audits Foster, inspire, and motivate team members to focus on continual improvement of products, processes and systems Analyze quality data in order to find areas for growth. Determining data-driven solutions and implementing quality improvement plans Oversee the efficient implementation of quality standards, programs, and processes to improve operational efficiencies and reduce/eliminate production waste. Interface with Suppliers for Certification/Quality Requests Support Supplier Quality Investigations with the Group Quality Team FAI creation and Review CoC Compliance Review/Approvals Support Group Quality Inspectors on various compliance activities Assistance with Customer Containment NOE Support Support creation and analysis of Group Supplier Quality Metrics EDUCATION AND EXPERIENCE Bachelor's Degree preferred or relevant experience equivalent to education Minimum 2 years' experience in supplier quality management or equivalent role. Previous experience in an aerospace, manufacturing environment highly desired. REQUIRED SKILLS Must have good analytical, problem-solving, and analytical skills Strong interpersonal and verbal and written communication skills Works well under pressure, prioritize projects and be deadline oriented Experience AS9100, ISO9001 or other ISO related standard desired Proficiency in Office 365. Excellent communication, interpersonal, and public speaking skills Excellent decision-making and problem-solving skills Strong organizational skills. Fluent in reading, writing and speaking/understanding English. Must be able to pass Visual Acuity requirements (color, depth perception and field of vision). This position requires use of information which is subject to compliance with the International Traffic in Arms Regulations (ITAR). 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. PHYSICAL REQIREMENTS Stationary Position: frequently remains stationary up to 90% of the time and sitting up to 8 hours in a day Move/Traverse: infrequently bend, stand, stoop and/or walk Carry Weight: infrequently carry weight and/or lift objects (light to heavy) weighing up to 10 pounds Hearing and Speech frequently communicates with the ability to hear and talk on a regular basis with employees, coworkers, and all personnel matters; must be able to exchange accurate information in these situations Sight: frequent use of sight to detect images on computer, office documents, and office objects near and far Climb: occasionally ascends/descends on stairway to get to office upper and lower floors.

The Quality Technician is responsible for ensuring product integrity throughout the production process. Key responsibilities include: Inspection Duties: Conduct incoming, in-process, and final inspections using tools such as calipers, micrometers, microscopes, and vision systems for micro parts. Lab Testing: Perform lab-based measurements including pH testing, viscosity, and moisture analysis using specialized equipment. Mechanical Testing: Execute pull force and burst testing to verify product durability and compliance. External Coordination: Schedule and coordinate specialized testing with external laboratories when needed. Final Visual Inspection: Ensure product quality through detailed visual assessments before release. This role is ideal for candidates with a strong attention to detail, hands-on experience with precision measurement tools, and the ability to communicate effectively with internal teams and external partners. Skills Inspection, testing, metrology, calipers, Quality inspection, Micrometer, Visual inspection, microscope Top Skills Details Inspection,testing,metrology Additional Skills & Qualifications 2-5 years of experience with hands on inspection Strong communication and reporting skills Experience within a Medical Device/Pharmaceutical is preferred, but not required Experience Level Intermediate Level Pay and Benefits The pay range for this position is $25.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Glendora,CA. Application Deadline This position is anticipated to close on Jul 21, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

2882 Whiptail Loop # 100 Carlsbad, CA 92010 T. ************ *************** Job Title: Quality Technician FLSA Status: Non-Exempt Reports To: Quality Manager Job Code: Department: Quality Date: May 2025 JOB SUMMARY The QC Technician position at Fluidra will be responsible (under limited supervision) of maintaining quality standards by recording any quality results and maintaining quality records per company policy. Collecting and compiling statistical quality data. This person will interact with the Materials Dept. (Receiving, Shipping, Production Planning/Scheduling and Inventory Control) personnel to assure accurate and efficient processing of material and disposition into the appropriate location (perform inspections, reworks, tests, and monitor material in the MRB location). They will also oversee MRB (Material Review Board) and of RMA (Return Material Authorization) and communicate issues with the supervisor and/or the Quality Engineering. Other or change in duties may apply depending on company needs. DUTIES & ESSENTIAL JOB FUNCTIONS ● Make acceptance or rejection decisions based on established procedures and materials inspections. ● Interpret and apply common attributes-based (e.g., ANSI Z1.4) and variables-based (e.g., ANSI Z1.9) sampling plans to acceptance activities. ● Have experience in the process used to manage non-conforming product (i.e., MRB) ● Keeps detailed records of inspections, rewoks, and defect reports. ● Be able to read, comprehend and follow written procedures/instructions. ● Be able to interpret and understand mechanical drawings, assembly drawings and BoM for inspection and rework processes. ● Be able to utilize ERP/MRP systems as necessary to determine/record key information (Oracle & Epicor) as well as disposition of received products. ● Accurately document the results of the inspections and testing. ● Assist in the writing and updating Inspection procedures, protocol, and checklists. ● Independently determine appropriate rework/inspection setups using the equipment available ● Be able to locate certain product in warehouse and segregate from Finished Goods ● Be able to perform and oversee rework operations ● Be able to manage RTV (Return to vendor) product accurately. ● Perform other duties as assigned. OTHER FUNCTIONS AND RESPONSIBILITES Improving and maintaining role KPI's Support other departments and key roles withing the DC. QUALIFICATIONS 3+ years of quality control inspection experience or equivalent combination of education and experience required to perform at this level. Ability to interpret engineering specifications/drawings. Interpersonal skills and written and oral communication skills sufficient to train others in the use of inspection equipment and procedures, accurately completes paperwork, understands documentation and effectively communicates with fellow employees. Extreme attention-to-detail, especially in the documentation of first articles to distinguish all details and requirements of a first article (tolerances, parts set ups, etc). General proficiency of Microsoft Excel and Microsoft Word. Analytical Skills. Attention to Detail 2-3 years' operating a forklift Fluency in English- able to read, write, speak and interpersonal communications EDUCATION HS Diploma or Equivalent PHYSICAL REQUIREMENTS While performing the duties of this job, employees are regularly required to read and write, walk within parcel station to access documents, stand primarily; talk or hear, both in person and by telephone; use hands repetitively to finger, handle, feel or operate standard shipping and DC equipment; reach with hands and arms and lift up to 20 pounds. They also occasionally move and lift objects weighing up to 75 pounds. Specific vision abilities required by this job include close vision, distance vision and the ability to adjust focus.

The Company Zurn Elkay Water Solutions Corporation is a thriving, values-driven company focused on doing the right things. We're a fast growing, publicly traded company (NYSE: ZWS), with an enduring reputation for integrity, giving back, and providing an engaging, inclusive environment where careers flourish and grow. Named by Newsweek as One of America's Most Responsible Companies and an Energage USA Top Workplace, at Zurn Elkay Water Solutions Corporation, we never forget that our people are at the center of what makes us successful. They are the driving force behind our superior quality, product ingenuity, and exceptional customer experience. Our commitment to our people and their professional development is a recipe for success that has fueled our growth for over 100 years, as one of today's leading international suppliers of plumbing and water delivery solutions. Headquartered in Milwaukee, WI, Zurn Elkay Water Solutions Corporation employs over 2800 employees worldwide, working from 24 locations across the U.S., China, Canada, Dubai, and Mexico, with sales offices available around the globe. We hope you'll visit our website and learn more about Zurn Elkay at zurnelkay.com. If you're ready to join a company where what you do makes a difference and you have pride in the work you are doing, talk to us about joining the Zurn Elkay Water Solutions Corporation family! If you are a current employee, please navigate here to apply internally. The Quality Technician II is responsible for working with production, shipping and suppliers to ensure that product received, manufactured, and shipped from an assigned Zurn location to meets quality standards. Key Accountabilities * Support Operations with inbound and in-process inspections and problem solving to prevent quality escapes working with internal engineering and other key stakeholders * Ensure tools are calibrated per IAPMO standards * Check manufacturing work and record problems and resolution in the Quality Management System * Execute inbound inspections from suppliers to ensure inbound product compliance; work with and collect process data as required; write summaries to validate or show deviations from existing standards * Perform receiving, in process, and final inspection activities * Perform internal manufacturing process and product audits as directed * Support quality management system audits * Report supplier nonconformances through the Global Supplier Quality reporting system and business unit systems and to cross functional stakeholders. Collaborate with Global Supplier Quality team to resolve supplier quality issues. * Assist with nonconforming material containment process within the business unit * Communicate with quality department team and internal disciplines to communicate and resolve customer quality concerns * May be assigned to participate in projects as a part of development as assigned by Quality System or Engineering supervision / support team * Support quality department with Corrective and Preventive Action Process * Perform nonconforming material analysis as directed * Collect process data as required and maintain quality records * Support continual improvement (#CI) objectives as assigned * Continually learn and successfully execute processes to meet organizational objectives * Other projects as assigned Qualifications/Requirements * High School/GED required * 5 years experience as a Quality Technician preferably in a fabrication or manufacturing environment * Demonstrated communication and problem solving capabilities * Knowledge of blueprint reading * MS Office (Word / Excel / Power Point /Outlook) knowledge required * Can work with Hand Gauges (calipers, micrometers, etc.) * Proficient computer skills * Excellent communication and teamwork ability The compensation range identified below are a good faith estimate of the salary expected to be paid as performed from these locations. Actual salaries may vary based on compensable factors including but not limited to skillset, experience, education and training, and other relevant business and organizational factors. Most candidates will start in the lower half of the range. Hourly Range: $25-31/hour Total Rewards and Benefits * Competitive Salary * Medical, Dental, Vision, STD, LTD, AD&D, and Life Insurance * Matching 401(k) Contribution * Health Savings Account * Up to 3 Weeks Vacation * 12 Paid Holidays * Annual Bonus Eligibility * Educational Reimbursement * Matching Gift Program THIRD PARTY AGENCY: Any unsolicited submissions received from recruitment agencies will be considered property of Zurn Elkay, and we will not be liable for any fees or obligations related to those submissions. Equal Opportunity Employer - Minority/Female/Disability/Veteran

The Quality Technician, under minimum supervision, shall perform quality assurance activities such as incoming inspection, in-process inspection, and final inspection. Essential Functions Follow all employee guidelines and Quality System requirements as defined by ClearPath Medicals practices, policies and Standard Operating Procedures to ensure customer and FDA requirements are met. Demonstrate knowledge and act in accordance with ClearPath Medicals Employee Guidelines and applicable quality standards as outlined in ClearPath Medicals Quality Manual. Perform incoming inspection activities, including first article inspection. Perform in-process inspection, including periodic audits of manufacturing work-in-process. Perform final inspection and release, including review of paperwork to ensure that all required inspections and traceability have been documented. Coordinate preventive maintenance and calibration activities. Accurately record process documentation. Must be able to thoroughly interpret, read and follow all work instructions, assembly drawings and other manufacturing/test documentation. Perform other duties as assigned. Must comply with all safety requirements. Required Education Required: Minimum High School diploma or GED. Preferred: Two-year degree (Associates or technical certification) in electronics/advanced mechanics or an equivalent combination of education and relevant work experience in medical devices within a QSR/FDA regulated environment. Required Skills Basic measurement skills using a variety of hand tools and electronic equipment such as rulers, scales, micrometers, calipers, and similar items. General computer skills, including Excel spreadsheets. Simple math skills, including understanding of fractions, cross multiplication, and calculator use. Must be able to work in a fast-paced work environment while performing quality duties. Excellent hand and eye coordination. Excellent attendance and a positive attitude. Good written and oral communication skills; must have the ability to communicate effectively and project a professional image when giving and taking information in writing and in person. Ability to follow verbal and written instructions. Good analytical skills including the ability to identify potential problems. Attention to detail. Capable of both communicating and understanding the English language. Working knowledge of IPC 610, IPC 620, and J-STD standards. Required Experience Previous quality experience in electro-mechanical assemblies and/or other medical devices is desired but not required.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for the formulation of powder media. 2nd Shift: 1:00 pm - 9:30 pm At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Responsibilities Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. Suggest changes in departmental procedures and processes (SOPs) as needed. Performs and documents line clearance at the start of each formulation event. Maintains all required logs and associated documentation. Assures that all chemicals are stored and labeled properly. Performs process scale checks on all required equipment including scales and balances. Keeps work area, utensils, tanks, mills, and equipment clean and organized. Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. Understands and follows procedures to ensure that chemicals are handled properly. Good understanding of metric system and its conversions. Follows and actively participates in sustaining the 6S program in the area. Other duties as requested by Lead or Supervisor. Required Skills/Education High School Diploma or equivalent Good work history. Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. 1-2 years of hands on experience General education about chemicals and proper handling (college level science preferred). Working knowledge of metric system. Good understanding of current Good Manufacturing Practices (cGMPs). Ability to speak, read, and write English. Good oral and written communication skills. Salary and Benefits: For California, the base hourly range for this position is $19.65 - $25.51. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). Medical, Dental, Vision Life Insurance 401k Paid Time Off *#LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

at Thompson Pipe Group - Los Angeles QC Technician Who We are: Thompson Pipe Group is a privately held family business of engineers, contractors, and manufacturers based in Rialto, California. From humble beginnings, we built a family of products to meet the needs of all kinds of infrastructure. Each generation of products is better than the previous. Thompson Pipe Group is now the largest and most diverse drainage, sanitary, pressure and trench-less pipe provider, with manufacturing locations across the country and serving not just the US but all North America. Please visit our website at ************************* :Thompson Pipe Group is currently looking for a Quality Control Technician who will work within the Quality department and alongside Production Operations to ensure the highest level of quality for Thompson Pipe Group products. The position will collaborate with various departments within the facility to ensure knowledge of, and compliance with, project-specific quality assurance requirements.Pay rate: $23/hr (DOE) Responsibilities • Under the supervision and direction of the supervisor, monitor all aspects of Quality • Steel Tensile Test reports • Aggregate tests • Joint Assembly Test reports • Production fabrication, test, and inspection reports • Assist Production personnel who have been assigned quality control responsibilities. • Ensure compliance with any additional or special quality assurance procedures required by project specifications. • Perform other duties as may be assigned by the supervisor.Desired Qualifications• Knowledge of concrete technology, welding, and nondestructive evaluation/testing (NDE/NDT) preferred but not required • ACI Field Grade 1 certification required • High school diploma or general education degree (GED). • Previous experience in a Quality Assurance or Production role in a similar industry preferred • Proficient in the Microsoft Office suite of applications. • Bilingual in English and Spanish. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. • Ability to lift up to 50 lbs. • Standing, walking, and stooping throughout the shift. • Ability to keep up with manufacturing requirements. • Ability to meet attendance schedule with dependability and consistency • Ability to use equipment and tools properly and safely. • Ability to lift heavy objects, walk and stand for long periods of time and perform strenuous physical labor under adverse field conditions. • Able to work with dust and outside environment conditions(i.e. rain, wind) • Use to wearing earplugs and other PPE - such as a hard hat, steel-toed boots, gloves, and safety glasses as required. Must pass Pre-employment Physical and drug test. Not A Warehouse Job. Precast Concrete Pipes is what we do. What We Offer Medical, Vision and Dental, Life Benefits Life & Supplement Life Company Matched 401K retirement plan Vacation & Sick Leave Training and Development Career Opportunity! $1,000.00 Referral Bonus Apply Now!We are located at 3009 N Laurel Avenue Rialto, CA 92377 Note: Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions upon request. Thompson pipe group is an Equal Employment Opportunity (EEO) employer that welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, gender identity, sexual orientation, religion or another legally protected status, or any other classification protected by federal, state, or local law. Drug-free workplace. EOE/AA - M/F/Vet/Disability

We are actively seeking an experienced *Cath Lab Technician* for a 13-week travel contract. This role requires proficiency in cardiovascular procedures and the ability to work in a dynamic, high-acuity environment. The ideal candidate must be ARRT certified and have prior *Cath Lab experience*. *Job Title: *Cath Lab Technician *Facility:* Lynwood, CA 90262 *Department:* Cardiac Catheterization *Skill: *Cath Lab Technician *Duration:* 13 Weeks *Job Type:* Travel Contract *Shift:* 7:00 AM - 7:30 PM (12-Hour Shifts) *Pay Rate:* $80.00/hr - $85.00/hr *Requirements:* * *ARRT Certification* - Required * *Previous Cath Lab experience* - Required * Current BLS certifications *Key Responsibilities:* * Assist in diagnostic and interventional cardiac catheterization procedures * Operate and monitor equipment during procedures * Maintain sterile field and ensure patient safety throughout * Document procedure details accurately and in a timely manner * Respond to emergencies and provide support to the clinical team Job Type: Contract Pay: $80.00 - $85.00 per hour Expected hours: 36 per week Medical Specialty: * Cath Lab Schedule: * 3x12 * Day shift Application Question(s): * Best time to call you? Experience: * Cath Lab Technician: 1 year (Required) License/Certification: * BLS Certification (Required) * ARRT Certification (Required) Ability to Commute: * Lynwood, CA 90262 (Required) Work Location: In person