Quality Control Technician Jobs in Montclair, CA

National Staffing Solutions-Surgical Services is seeking a travel Cath Lab Technologist for a travel job in Northridge, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 06/23/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel National Staffing Solutions-Surgical Services Job ID #70437984. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About National Staffing Solutions-Surgical Services National Staffing Solutions is a leader in the travel healthcare industry for over a decade. National Staffing Solutions places healthcare professionals in positions that allow them to gain valuable experiences, fill the skyrocketing demand in their field, and travel nationwide at premium pay. We use our insight, experience and nationwide resources to make exceptional connections every day! Through our many years of service, we are now positioned perfectly to pass your name and resume to our healthcare partners that are looking for YOUR help. Facilities across the nation choose National Staffing Solutions as their workforce partner to solve nursing shortages that range from quick-fill demands to areas in urgent need of medical attention. Hundreds of healthcare organizations throughout North America rely on us each year to connect them with quality professionals, like yourself, who are ready to work.

These are full-time (temporary 3-6 months, potential for temp-to-perm) on-site roles all located in Irvine, CA for a US Class II Medical Device company as follows: Senior Quality Engineers (2): NPD (1), Sustaining (1) Senior Manufacturing Engineer (1): SolidWorks proficiency required Quality Control Technician (1) Manufacturing Operators (14) Applicants must live near Irvine, CA, have previous medical device experience and be authorized to work in the United States. If interested, please submit your resume to *****************************.

Quality Control Inspector (Contract) Hours: 6:00 AM - 2:30 PM (may shift to 7:00 AM - 3:30 PM) Pay: $21 - $27/hr Contract: 6 Months (possible extension) About the Role: We're hiring a Quality Control Inspector to perform visual, dimensional, and functional inspections of components and finished medical device products. This role is hands-on, requiring blueprint interpretation, use of inspection tools (e.g., Keyence, hand tools), and strict adherence to GMP/GDP standards. Responsibilities: Perform receiving and in-process inspections, including FAIs. Use blueprints, GD&T, and tools to inspect parts. Measure and interpret critical vs. non-critical dimensions. Complete documentation: DHRs, COCs, labels, and QMS entries. Verify drawings vs. actual parts, conduct line clearances. Escalate nonconformances and support quality team feedback. Ensure compliance with SOPs, GDP, GMP, ISO 13485. Qualifications: 2+ years' QA/QC experience (GMP/GDP required). High school diploma or equivalent preferred. Proficient with inspection tools and basic computer skills. Strong attention to detail, manual dexterity, and documentation accuracy. Clear written and verbal English communication skills. Able to work independently and in teams. Interview Process: 30-minute phone screen Onsite interview with drawing interpretation and measurement test 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.

FDH Aero is a trusted global supply chain partner for aerospace and defense companies. With more than 55 years of experience, it specializes in c-class components that include hardware, electrical, chemical, and consumable products and services for global OEM and aftermarket customers. At FDH Aero, we understand that the strength of our brand comes from our people, and our culture empowers every team member to contribute and grow. As a global team, our culture is rooted in five (5) core values that begin with the words “We are” and include: service-first, respectful, amplifiers, open-minded and accountable. FDH Aero is headquartered in Commerce, California, and has operations across the Americas, EMEA and APAC. FDH Aero has locations in 14 countries across the globe, with more than 1,200 best-in-industry employees and over 650,000 square feet of inventory space. For more information, please visit the FDH Aero website. FDH Hardware, an FDH Aero Company is looking for a Quality Inspector III who will be responsible for inspecting, testing, and evaluating products and processes to ensure they meet quality standards and specification including communicating with suppliers/customers as needed and handles disposition and control of non-conforming product. Additionally, this individual will review and disposition all certification documentation to meet traceability requirements per drawing, AS standards, and Company Quality standards. They will perform First Articles for submission to customers and review and approval of First Articles from suppliers among other duties as assigned. Responsibilities: Conducts dimensional inspections per design record and documented AQL levels; Conducts visual inspections for obvious defects Review and disposition all certification documentation to meet traceability requirements per drawing, AS standards, and Company Quality standards Communicate with suppliers and customers as needed Disposition and control of non-conforming products Obtain and maintain Customer Designated Supplier Quality Representative Stamps (DSQR) for at least 3 customers Creation, review and submission of FAIR meeting AS9102 requirements Identify and communicate opportunities to increase inspector productivity and assist with RCCA activities pertaining to quality. Assist in internal, customer, and third-party audits 6S and general cleanliness of work area and warehouse Basic Qualifications: 5+ years of inspection experience in aerospace, or manufacturing environment Previous aerospace inspection experience preferred Experience in Quality inspection methods and procedures Experience in creation of First Article Inspection Reports Experience in being a Designated Supplier Quality Representative Experienced with Lockheed, Northrop, DCMA or similar Tier 1 OEM/Government Familiarity with Military and Industry Specifications and Standards Expert at creation, review and submission of First Article Inspection Report Strong analytical, organizational, and troubleshooting skills Knowledge of AS9120 requirements Experience in the usage of calipers, ring/pin gages, comparator, and Smart scope Proficient PC skills and use of Microsoft Office products (Outlook, Excel) Advanced GD&T Skills - Optical Comparator, CMM, Layout, Vision Scope Systems Ability to manage multiple and competing priorities Embodies the FDH Core Values

Job Title: Electronics Lab Technician Pay rate: $35/hr. Zip Code: 92780 Job Description: This is what you'll do: Support receiving and shipping of packages. Manage material inventories and kit parts for assembly and/or rework. Perform PCBA modifications such as component rework, soldering/de-soldering of electronic components, blue wire modifications per IPC-610 class 3. Build wire harnesses per IPC/WHMA A-620C standard. Build and/or setup custom test equipment per engineering diagrams/specifications. Conduct functional testing of electronic circuit assemblies and engineering prototypes. Perform unit assembly of ECU modules per engineering diagrams/specifications. Maintain accurate records of test results and update of procedures as needed. Troubleshoot to identify root cause of failures. Qualifications 2+ years of technician work experience in electronics/engineering labs Technology/Technician degree or equivalent experience Electric vehicle experience a plus Basic electrical understanding Excellent soldering and harnessing skills Familiar with test equipment such as multimeters, oscilloscopes, eloads, etc. Strong technical ability Ability to solder fine pitch ICs and 0402 components. Experience with MS office tools (Outlook/Excel/Word/PowerPoint/Project) Familiarity with Jira tools is a plus Python Scripting is a plus IPC-610, IPC-620, IPC-7711, IPC-7721 or J-STD-001 certifications are a plus

Extron is a leading developer and manufacturer of professional AV hardware and software solutions which serve the ever-changing needs of organizations around the world as they strive to better communicate. Each Extron product is carefully engineered to provide best-in-class performance, intuitive operation, and exceptional reliability. At Extron, the passion for our products is evidenced by our company culture, which encourages innovation and provides opportunities for individual career growth. Our teams develop and release over 100 new products a year and continue to grow our vast patent portfolio. Position Responsibilities include but not limited to: Participate in the Failure Review Board (FRB) to disposition Product fallout (i.e., Failures) after Incoming Inspection and Test. Coordinate audit of product from sub-contract manufacturers per existing guidelines. Execute internal audits for the ISO certification process. Perform data analysis and report results to Senior Management. Data analysis is designed to gain insight into special-cause events and common-cause capability issues and areas to reduce waste and defects. Review the Manufacturing Documentation Release System for accuracy on new products. Will develop visual reports and dashboards using Power BI. Perform shelf-life audits. Minimum Qualifications: BA/ BS in Quality Engineering or any related Engineering field. 6+ years of experience in Quality Control in an electronics manufacturing environment, preferably audio/video equipment. Supervisory/leadership experience a plus. ASQ certification a plus. Must possess extensive knowledge of various Operational/Manufacturing Processes including, but not limited to the below: In Process Inspection of Manufacturing Processes for Mechanical Assembly and Test of Electronic Products. Receiving Inspection, Control & Disposition of Nonconforming Material. PCB Fabrication (ANSI IPC 600 & 6010). PCBA Assembly (ANSI IPC 610). Excellent problem solving skills related to process analysis and continuous improvement based on quality and efficiency metrics. Knowledge of Process Data collection, Analysis, Charting, Incorporation of Engineering Change requests with the ability to communicate the results to various levels of Management. Experience in the ISO 9000 requirements, with the ability to write Departmental/ Process procedures and a thorough understanding of Corrective Actions, Internal Auditing, and RBT. Excellent communication skills (written and verbal). Strong attention to detail, highly organized, computer literate, and must be hands on. Ability to work well in a fast-paced professional office environment. Salary Range: $100,000 to $105,000. Pay may vary depending on experience, qualifications, and other job-related factors.

Role: Senior Aerospace Laboratory Technician Salary: $70,000 - $100,000 Clearance: MUST be Secret cleared or higher A leading Military Aircraft Group is seeking a Senior Aerospace Laboratory Technician in Torrance, CA. This onsite role reports to the Site Engineering Lab Manager and requires an active DoD Secret Clearance. Key Qualifications: Background in mechanical, hydraulic, or electromechanical testing Experience testing to RTCA DO-160 or MIL-STD-810 (preferred) Proficiency with hand tools, test instruments, and lab equipment Familiarity with LabView, DIAdem, dSPACE, Dewesoft, or MATLAB (preferred) Responsibilities: Conduct environmental and functional tests for product development & qualification Maintain safety standards in a hazardous lab environment Set up, inspect, and operate test equipment per procedures Analyze test data, troubleshoot anomalies, and support engineers Prepare detailed test logs, reports, and documentation Provide training and collaborate across teams Benefits: Annual Profit sharing Employer matched 401k Employee stock purchase plan Health and spending saving account Comprehensive medical, dental, vision, life, disability plan Tuition assistance Growth, to achieve internal promotions This is an exciting opportunity for a highly skilled lab technician to play a key role in aerospace innovation. Apply today!

This position is primarily responsible for overseeing quality control tasks, including conducting receiving inspections, in-process inspections, and final inspections. Supervise the daily activities of the Quality Control Department, under direct management of the Quality Assurance Manager. We are looking for someone with 5+ years of quality experience in either the medical device or aerospace industries. ...

An American electric vehicle manufacturing company is actively looking for a detail-oriented Electronics Lab Technician to join their team. This is an initial 5-month CT role with potential for extension located in their Tustin, CA location. It is Monday-Friday, first shift hours. If you have an adventurous spirit and are hardwired with curiosity this is the perfect company to be a part of. They have great company culture, exciting technology and endless opportunities for learning and growth. As the Electronics Lab Technician one will be responsible for a wide range of tasks relating to the testing, validation, and repair of Rivian's electronic components and systems. Required Skills & Experience 2+ years of technician work experience in electronics/engineering labs Technology/Technician degree or equivalent experience Basic electrical understanding Excellent soldering and harnessing skills Familiar with test equipment such as multimeters, oscilloscopes, eloads, etc. Strong technical ability Ability to solder fine pitch ICs and 0402 components. Experience with MS office tools (Outlook/Excel/Word/PowerPoint/Project) Desired Skills & Experience Python Scripting is a plus Electric vehicle experience a plus Familiarity with Jira tools is a plus IPC-610, IPC-620, IPC-7711, IPC-7721 or J-STD-001 certifications are a plus What You Will Be Doing Daily Responsibilities: Support receiving and shipping of packages. Manage material inventories and kit parts for assembly and/or rework. Perform PCBA modifications such as component rework, soldering/de-soldering of electronic components, blue wire modifications per IPC-610 class 3. Build wire harnesses per IPC/WHMA A-620C standard. Build and/or setup custom test equipment per engineering diagrams/specifications. Conduct functional testing of electronic circuit assemblies and engineering prototypes. Perform unit assembly of ECU modules per engineering diagrams/specifications. Maintain accurate records of test results and update of procedures as needed. Troubleshoot to identify root cause of failures. Applicants must be currently authorized to work in the US on a full-time basis now and in the future.

Prepares reagents. Performs quality control (QC) testing on barcoded magnetic beads (BMB), incoming raw materials, in-process reagents, diagnostic products, product stability, and analyzers. Responsibilities · · Performs QC testing on all ABC products, analyzes and plots data, performs statistical trend analysis. · Prepares and qualifies QC reagents · Complies with all QC procedures. · Provides schedules and meets deadlines. · Coordinates partnership with Manufacturing, Research and QA Groups. · Investigates NCM and CAPA. · Calibrates, monitors and ensures equipment performance. · Ensures clear and accurate batch records. · Writes and updates operating procedures. · Maintains a high degree of safety awareness and a clean orderly work area. Qualifications · Bachelor's degree in life science. Relevant laboratory experience in diagnostic manufacturing, QC testing, and familiar with general laboratory techniques.

As a Cleaning Employee you are responsible for carrying out cleaning activities in the cleanrooms (a ""clean"" work environment where pharmaceutical treatments are applied). Your activities therefore take place under strict quality requirements that the pharmaceutical industry must adhere to (GMP, 'Good Manufacturing Practices' rules). He / she ensures that aseptic (sterile) and hygienic conditions are maintained and that the accompanying documentation is accurately completed. You play an important role in guaranteeing the hygienic conditions of the cleanrooms. Perform sanitary cleaning operations in a sterile environment in accordance with strict procedures and as prescribed by the supervisor Stocking sterile and non-sterile protective garments for multiple locker rooms in the correct order Ensuring accurate and complete documentation and signing it Taking training courses that are required in accordance with the company's procedures and policies Ensuring an accurate and complete inventory of cleaning products, so that sufficient stock is available Experience: High School Diploma Knowledge / experience Required Following the cleanroom protocols (working according to the strict rules, regulations and procedures of the company) Prepare to work in a sterile environment where biological and hazardous waste is processed and disposed of on a daily basis Able to work in a team-oriented environment Able to read documents (prepared in English), such as standard operating procedures, operating manuals, and company and safety policies Prepare to work at night and work overtime if necessary Possesses a strong work ethic, reliable and punctual Good interpersonal, verbal and written communication skills Comfortable in a fast-changing organization Cleaning experience in a cleanroom / cGMP environment is a plus. Additional requirements Physically able, and willing to wear protective clothing and equipment, such as goggles, face shield and protective gloves Willing to work night shifts and weekends

Minimum 1+ years Cath Lab experience required. Soliant Health is seeking Travel Cath Lab / IRTechs for a hospital in Glendale, CA- About the assignment- Start date- as soon as possible 13 week assignment Schedule: Days 5x8s Facility will accept first time travelers ARRT / BLS / ACLS required Qualifications Travel experience - preferred but not required Minimum 2 Years Cath Lab Techexperience Why travel with Soliant? - Competitive Weekly Salary - Maximum Travel Stipends - Extensive Medical/Dental Insurance Offered - Matching 401(k) Plan - Travel Assistance - Premium Recruitment

RxSight is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world's first and only adjustable intraocular lens (IOL) that is customized after cataract surgery. The company's mission is to revolutionize the premium cataract surgery experience by allowing surgeons to partner with their patients to achieve optimized results for every unique eye. OVERVIEW: Performs quality functions to support IS013485, FDA, CGMP, Quality System Regulations, management reporting, LAL production/QA/QC, chemistry QA/QC, product release, in-process inspection, incoming inspection, quality process improvements for LDD, manufacturing transfer, and facility support. ESSENTIAL DUTIES AND RESPONSIBILITIES: Read, comprehend, and follow documents related to manufacturing, inspection and quality systems for audits, compliance, and implementation. Audit and approve production records. Verify production process via auditing/observation and testing. Inspect process output and product parameters against specifications. Ensure routine compliance with process steps and proper documentation of records. Maintain raw material lot information, monitor expiration date, and quarantine inventory when materials are expired. Performs incoming inspection on raw materials and incoming sub-assemblies/finished goods. Collect data for process, quality system, manufacturing quality and performance metrics and generate reports for management review. Identify non-conformances, deviations, non-compliance, lack of calibration etc. and propose corrective actions to management. Facilitate Manufacturing Review Board and supports non-conformance decision process. Govern and transact materials physically and through electronic system. Monitors laboratory and engineering equipment to ensure compliance with preventive maintenance and calibration programs. Performs laboratory notebook audits, inventory audits, and maintains QA retains. Take initiatives for the process improvements changes as related to manufactured components and finished products for LAL. Responsible for assisting the Quality Assurance team with any ad hoc reports and assignments as required. Perform incoming inspection and lot control activities of materials and parts. Assist Quality, Manufacturing and R&D groups in running validation, verification, and developmental studies, and defining processes. Development of inspection techniques and transfer to production and everyday use. Monitor gowning and cleanroom logbook check per SOP to ensure all section of the cleaning log has been filled accurately and completely. Provide Good Manufacturing Practices (GMP) and Quality Standard Operating Procedures (SOP) training to relevant department. Create and review First Article Inspection Reports when necessary. Requirements REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES: 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. Prior experience of working in cleanroom environment and/ or medical device manufacturing is highly preferred. Professional, responsible, energetic, and accountable. Excellent communication skills. Intellectually curious and eager to learn. Individual must be Quality oriented and possess a natural ability to pay attention to details. EDUCATION, EXPERIENCE, and TRAINING: Associate degree (A.A.) or equivalent from a two-year college or technical school; six months to one-year related experience and/or training; or equivalent combination of education and experience. Experience within a medical device company or regulated industry preferred. Microsoft Word; Microsoft Excel Training to be completed per the training plan for this position as maintained in the document control system. COMPUTER SKILLS: Microsoft Word; Microsoft Excel; Microsoft Access; QuickBooks. Salary Description $25.00 To $26.00 Per Hour

About Harbinger Harbinger is an American commercial electric vehicle (EV) company on a mission to transform an industry starving for innovation. Harbinger's best-in-class team of EV, battery, and drivetrain experts have pooled their deep experience to support the growing demand for medium-duty EVs and Hybrids. Leveraging a foundation of proprietary, in-house developed vehicle technologies designed specifically for commercial and specialty vehicles, Harbinger is bringing a first-of-its-kind EV platform to market, priced at acquisition parity to traditional diesel vehicles. Harbinger: Familiar Form, Revolutionary Foundation. Job Overview As a Quality Technician, GA/Chassis, you will play a crucial role in ensuring the quality and reliability of our EV platform. You will be responsible for conducting thorough inspections, implementing quality control measures, and collaborating with cross-functional teams to maintain and improve our production standards. You may also be required to maintain calibrated test equipment, prepare test data, and identify areas for quality control improvement. What You'll Do: * Inspection and Testing: Conduct detailed inspections of automotive components and finished products to ensure compliance with quality standards and specifications * Quality Control: Implement and maintain quality control processes throughout the production cycle * Continuous Improvement: Actively participate in root cause analysis and corrective action initiatives to address quality issues and prevent recurrence * Collaboration: Work closely with production teams, engineers, and other stakeholders to communicate quality standards and expectations * Training and Development: Provide training to production staff on quality control procedures and best practices Who You Are: * High school diploma required (College degree or equivalent preferred but not required) * 2 or more years of experience in a Manufacturing, Quality, or Process focused role * Strong mechanical aptitude and trouble-shooting skills * Excellent attention to detail and analytical skills * Effective communication and collaboration skills * Strong understanding of chassis or automotive assembly is preferred California Pay Range $25-$32 USD Equal Opportunity Harbinger is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, ancestry, sex, sexual orientation, gender, gender expression, gender identity, genetic information or characteristics, physical or mental disability, marital/domestic partner status, age, military/veteran status, medical condition, or any other characteristic protected by law. Harbinger is committed to ensuring that our hiring process is accessible for persons with disabilities. If you have a disability or limitation, such as those covered by the Americans with Disabilities Act, that requires accommodations to assist you in the search and application process, please email us at ************************. Candidate Data Privacy Harbinger may collect, use and disclose your personal information or personal data (within the meaning of the applicable data protection laws) when you apply for employment and/or participate in our recruitment processes ("Candidate Personal Data"). This data includes contact, demographic, communications, educational, professional, employment, social media/website, network/device, recruiting system usage/interaction, security and preference information. Harbinger may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering into an employment contract with you; (iv) complying with our legal, regulatory and corporate governance obligations; (v) recordkeeping; (vi) ensuring network and information security and preventing fraud; and (vii) as otherwise required or permitted by applicable law. Harbinger may share your Candidate Personal Data with (i) internal personnel who have a need to know such information in order to perform their duties, including individuals on our HR, legal, and finance teams, and the team(s) with the position(s) for which you are applying; (ii) Harbinger affiliates; and (iii) Harbinger's service providers, including providers of background checks, staffing services, and cloud services. Harbinger may transfer or store internationally your Candidate Personal Data, including to or in the United States, Canada, the United Kingdom, and the European Union and in the cloud, and this data may be subject to the laws and accessible to the courts, law enforcement and national security authorities of such jurisdictions. Please note that we are currently not accepting applications from third party application services. Any unsolicited resumes or candidate profiles submitted in response to our job posting shall be considered the property of Harbinger and are not subject to payment of referral or placement fees if any such candidate is later hired by Harbinger unless you have a signed written agreement in place with us which covers the applicable job posting.

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, 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. 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 (*******************).

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, 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. 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 (*******************).

Engineering company is seeking a Quality Technician to join their team. Schedule: 1st and 2nd shift. Mon - Fri 7am - 3:30pm 3:30pm - 12am Starting Pay: $18+, DOE. A Quality Technician is responsible for: Operation of measuring instruments and equipment for inspection of product Understands calibration/verification of measuring instruments. Verify conformance of product in accordance with Quality Plans (i.e., using visual inspection techniques, microscopes, micrometers, automated measuring instruments). Understands the fundamentals of the quality management system. Reads and interprets drawings. Understands defect types, sorting and lot control procedures. Performs work in accordance with traveler and work instructions. Performs technical end of shift duties, end of job procedures, and housekeeping procedures. Observes safety policies including personal protective equipment requirements and hazardous/emergency procedures. To be Considered you need: High School Diploma or GED Interprets instructions both written and oral. Must be able to occasionally exert push force up to 50 pounds

National Staffing Solutions-Surgical Services is seeking a travel Cath Lab Technologist for a travel job in Glendale, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 06/23/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel National Staffing Solutions-Surgical Services Job ID #70158601. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About National Staffing Solutions-Surgical Services National Staffing Solutions is a leader in the travel healthcare industry for over a decade. National Staffing Solutions places healthcare professionals in positions that allow them to gain valuable experiences, fill the skyrocketing demand in their field, and travel nationwide at premium pay. We use our insight, experience and nationwide resources to make exceptional connections every day! Through our many years of service, we are now positioned perfectly to pass your name and resume to our healthcare partners that are looking for YOUR help. Facilities across the nation choose National Staffing Solutions as their workforce partner to solve nursing shortages that range from quick-fill demands to areas in urgent need of medical attention. Hundreds of healthcare organizations throughout North America rely on us each year to connect them with quality professionals, like yourself, who are ready to work.

🔍 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.