Quality Control Analyst jobs in Santa Clara, CA

Ultimate Staffing is seeking R&D Technicians for our client in San Jose. This is a 100% onsite role with a starting pay of $25-$32 an hour based on experience. Please read the job responsibillites before applying. This is NOT AN ENTRY LEVEL ROLE. Shift : Monday-Friday 0630-1500 Responsibilities: In accordance with all safety policies and procedures, you will collaborate with scientists and engineers to support their experiments. Operate automation tools to build proprietary devices per SOPs or with engineer's oversight. Run metrology tools and assist with general lab work to support tool optimization experiments Document daily experiments and communicate completion status using MS Office applications. Notice and give feedback for anomalies or unexpected results. Minimum Requirements: A minimum of a high school diploma with at least 3 years experience in a lab R&D environment A commitment to delivering high quality results Basic computer software skills, including Microsoft Office and a browser. Preferred: Able to handle a dynamic research environment. Ready to learn a range of lab skills. Flexible and can collaborate on different projects with researchers. Comfortable using software for task completion and logging data. Physical Requirements: Working in a dry room. 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.

Job Title: R&D Chemist II Department: Research & Development Reports to: R&D Manager Employment Type: Full-Time FLSA Status: Non-Exempt The R&D Chemist II supports the development of personal care and color cosmetic products under the direct supervision of the R&D Manager. This role is responsible for creating and modifying formulations, conducting laboratory tests, maintaining detailed documentation, and collaborating with cross-functional teams to meet client requirements and project deadlines. Essential Duties and Responsibilities Develop formulations based on Product Development Requests (PDRs) from clients. Prepare lab-scale batches for personal care and color cosmetic products. Test and evaluate batches for performance, stability, and compliance with customer specifications. Conduct and monitor stability testing on lab batches and document results. Troubleshoot and optimize existing formulations to improve performance or resolve issues. Assist with pilot batches and monitor production processes as needed. Generate ingredient lists and provide technical documentation to clients. Maintain accurate records of batch formulations, modifications, and stability data. Participate in meetings with customers and raw material vendors. Ensure laboratory cleanliness, organization, and compliance with safety protocols. Stay up to date on industry trends and innovations by reviewing publications and raw material literature. Communicate project updates and findings clearly to internal teams and clients. Perform other duties and special projects as assigned. QualificationsEducation and Experience Bachelor's Degree in Chemistry or a related scientific field. 5-7 years of product development experience in the personal care or cosmetics industry. Knowledge, Skills, and Abilities Strong ability to follow technical formulations and instructions. Solid mathematical skills for precise formulation measurements. In-depth knowledge of raw materials and product development in the skincare/cosmetic industry. Excellent verbal and written communication skills. Proficient in Microsoft Office and formulation/database software. Highly detail-oriented with strong documentation and organizational skills. Ability to multitask and manage time effectively in a fast-paced environment. Team-oriented with the ability to work independently under minimal supervision. Resilient under pressure and capable of meeting tight deadlines. Physical Requirements and Work Environment Must be able to stand for extended periods. Frequent use of hands for laboratory tasks; regular reaching with arms and hands. Occasional lifting and/or moving of items up to 20 pounds. Willingness to work overtime and weekends when necessary.

We are seeking to hire a Quality Inspector to support our client in San Jose. Our client is a storage software manufacturer. Do you enjoy working with your hands? Do you have strong attention to detail? This is the opportunity for you! ESSENTIAL DUTIES AND RESPONSIBILITIES: The essential functions and responsibilities for this position include, but are not limited to, the following. Other duties may be assigned as needed. Conduct rigorous inspections on a wide range of products, including storage devices, servers, components, and returned systems and components to ensure they meet stringent quality standards and precise work instructions. Perform inspections at various stages of the manufacturing process, including Incoming Quality Control (IQC), In-Process Quality Control (In-Process QC), and Final Quality Control (Final QC), ensuring product quality at every step. Extensively inspect components in the Return Merchandise Authorization (RMA) process, covering RMA Incoming Quality Control (RMA IQC), RMA In-Process Quality Control (RMA In-Process), and RMA Final Quality Control (RMA Final QC), meticulously reviewing returned items for compliance with quality standards. Verify the correctness of parts used, cross-referencing them with the Bill of Materials (BOM) and Print Documents, and meticulously record inspection results and findings in applicable data sheets, forms, and records. Exercise judgment in reviewing and approving solutions, promptly escalating unacceptable responses to the Quality Supervisor for further action, all while adhering to company policies and procedures. Uphold a positive attitude, making valuable contributions to the team effort, and readily assisting or providing coverage for other QC inspectors when required. Assume responsibility for maintaining the cleanliness, safety, and organization of the work area to ensure a conducive and productive environment. Flexibly perform any other duties as assigned by Quality Management, providing comprehensive support to maintain product quality and adherence to company standards. JOB LOCATION: Campbell, CA 95008 SHIFTS AVAILABLE: Day shift 8:00 AM - 6:30 PM Monday-Friday. OT as needed. JOB TYPES: Full-Time, Contract-Hire PAY: $23.00 per hr BENEFITS: Dental insurance Health insurance Vision insurance WORK LOCATION: In-Person Apply now and one of our recruiters will reach out to you! Balance Staffing is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity Veteran status, or any other characteristic protected by federal or state law.

AOSense, Inc. is the leading developer and manufacturer of innovative quantum technologies employing atom optics. Our products use frequency-stabilized lasers and atoms in a vacuum cell to measure accelerations, rotations, magnetic fields, and time with unparalleled accuracy and stability. Our staff includes physicists, engineers, and technicians with expertise covering a wide array of disciplines. Our teams are dynamic and fast paced since our hardware is cutting edge. POSITION SUMMARY: We are seeking an R&D technician who specializes in precision assembly and testing. As a hands-on R&D Technician at AOSense, you will work with physicists and engineers to build and test high-performance, fieldable accelerometers, gyroscopes, gravimeters, atomic clocks, frequency standards, and magnetometers, as well as component technologies that we sell commercially to the R&D community. RESPONSIBILITIES: Collaborate with physicists and engineers to assemble and test complex quantum sensor and atomic clock hardware Procure and track inventories of mechanical, optical, vacuum, and electrical components Coordinate component and subsystem fabrication, assembly, and test Assemble precision mechanical systems Align lasers through optical systems Procure and maintain laboratory equipment and supplies Collaborate with engineers to define and implement test plans Bake out and leak test vacuum systems Document and report results of validation testing Requirements Demonstrated success in precision mechanical assembly of prototypes and products Enthusiasm for developing expertise in new fabrication disciplines Proven organizational skills and attention to detail Hands-on experience with test equipment Excellent troubleshooting skills Applicants should thrive in a dynamic environment U.S. Government contracts require applicants to be U.S. citizens or permanent residents DESIRED EXPERIENCE: Expertise aligning and securing micro-optical components Hands-on experience with vacuum system assembly and testing Adept in glovebox assembly work Sensitivity to cleanliness requirements of vacuum and optical assemblies Skilled in mechanical prototyping, including basic machining and finishing operations Practical experience with advanced bonding methods, including soldering, brazing, and adhesives Proficiency with SolidWorks mechanical design software Familiarity with electronics prototyping, including reading schematics, PCB fabrication, assembly, soldering, and rework Experience testing low-noise analog, mixed-signal, and rf electronics Basic knowledge of data acquisition and analysis software such as LabVIEW, MATLAB, and Python EDUCATION AND EXPERIENCE: Associate degree in a relevant technical field or equivalent professional experience, with experience in an R&D environment Benefits Salary depends on qualifications and experience Medical and dental Retirement Stock plan AOSense is an equal opportunity employer (EOE) and considers qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran or disability status, or any other federal, state or local protected class. AOSense is committed to providing equal employment opportunity to qualified individuals with disabilities. If you are disabled and require special assistance or a reasonable accommodation while seeking employment with AOSense, then please contact us via email at ******************* or call ************** x210

Job Description Vegetation Management Quality Control Specialist Who are we? We’re dedicated to the growth of our employees. We truly believe in your development. For those who show initiative, we will do what it takes to get you where you want to go. We’re growing but still maintain an entrepreneurial spirit. We give you room to be accountable and responsible in your role. We believe progress is bred through innovation and we encourage our employees to bring their ideas forward. We’re safety focused. Safety is paramount in how we operate as we believe in providing excellence in our service to our vegetation management clients. We’re transparent and respectful. We support each other and are transparent and honest in our communication. We believe that trust is the foundation of our success with clients and within our team. Who You Are: You’re energetic and enjoy working outdoors. You understand that this space can be demanding, and you are equipped with the skills necessary to get the job done. You have at least seven years of combined experience. Bachelor’s degree with 3 years of field experience. Associate degree with 5 years’ experience. 7 years of utility vegetation management experience. Responsibilities: Accurately identify dead and dying trees affected by drought and other environmental conditions. Inspect overhead power lines for proper vegetation clearance Perform Quality Control assessments on pre-inspection and tree-trimming work Document information for client ’s vegetation management program Inspect and assess trees for hazard or danger potential Audit tree contractor's work for compliance with client specifications and needs Assist in storm and emergency situations and other miscellaneous line clearance projects Communicate daily with the client, contractors, landowners, and public. Perform duties in a manner that promotes and maintains good public relations. Assume other duties and responsibilities as assigned. Qualifications: Bachelor’s or Associate degree in forestry, Environmental Science, or related field preferred ISA (International Society of Arboriculture) Certified Arborist Designation preferred. Note - Some projects may require ISA Arborist certification and/or Tree Risk Assessment Qualification (TRAQ) ISA Utility Specialist certification preferred Experience in Forestry, Arboriculture, or Horticulture a plus Must possess tree identification skills and the ability to read maps Must have exceptional written and verbal communication skills, strong problem-solving capabilities, the ability to multi-task, and attention to detail Must be able to work alone, outdoors in various weather conditions and terrain Must be skilled with technology and possess basic computer and smart phone skills Capable of operating a 4x4 vehicle on rough roads Bilingual (English and Spanish) is a plus Physical Demands, Conditions, Work Environment The physical demands, conditions, and work environment characteristics described here 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. Employees must be able to maintain attention and concentration for extended periods of time. Work alone in an outdoor field environment; extensive vehicle operation and foot patrol of utility power lines; remote locations as well as urban, city environment; physical demands and travel from site to site, including walking/hiking on various surfaces including flat, dry, wet, slippery, uneven, rough, steep terrain, hills, and slopes; exposure to noise, dust, grease, and all types of weather and temperature conditions; exposure to hazardous traffic conditions. Physical Primary functions require sufficient physical ability and mobility to work in a field environment: walk, stand, sit, and operate a motor vehicle for prolonged periods of time; frequently stoop, bend, kneel, crouch, run, crawl, climb, reach, twist, grasp and make repetitive hand movements in the performance of daily duties; carry, push and/or pull light to moderate amounts of weight (5 to 10 lbs.); operate assigned equipment and vehicles; verbally communicate to exchange information with public; see and hear in normal range with or without correction; operate assigned field equipment, including handheld computer, range finder, water backpack, shovel, and traffic cone. Safety Safety is a top priority at Atlas Field Services. Successful candidates will be committed to their personal safety and to the safety of others. This role will require a general understanding and the ability to identify safety hazards and report any unsafe working conditions. The position requires active participation in safety briefings and may deliver industry-specific safety messages to a broad audience when called upon. Pre-Qualifications Applicants must pass a pre-employment drug test. All candidates must possess a valid driver's license and have a good driving record. Job Type – Full Time Compensation Range - $44 - $51 per hour AFS is an Equal Opportunity Employer

Job Description Shift: 3rd shift, graveyard (shift begins: 10pm) ********************************************************************************* Performs a variety of inspection procedures to ensure quality levels at various stages of manufacturing at or above the standard. Support the organization goals in achieving total customer satisfaction. Key Responsibilities: Inspect in-process or finished production assemblies and sub-assemblies for conformance to quality assurance standards Working from blueprint, engineering change notices, or established operating procedures determine acceptance or rejection or rework requirements of a part May evaluate new procedures for non-standard rest and perform special set-up on new equipment Assist others in correcting or preventing deficiencies in quality or workmanship Give work direction to other inspectors Know your customers' expectations and drive action to meet them Perform first article process Identify component Perform related work as assigned Job Qualifications: Education: Secondary/High School, Certificate Diploma Experience: 6+ Years preferably in Quality a plus Required skill: PCBA Experienced Able to use measurement equipment. Must be able to read ECO/Dev instruction/build drawer and BOM. Familiar with SMT and identify component, IPC 610 Knowledge and preferred IPC Cert. Familiar w/ First Piece and First Article process. Job Competencies: Attention to detail Communication skills - verbal and written Organized and good critical thinking skills Data collection, management and analysis Team work Ability to interpret complex customer rules and regulations Demonstrated skills in project management and ability to train others to lead projects Works well independently Excellent interpersonal and communication skills Ability to manage time and prioritize multiple task in a fast paced environment Proficient in use of MS Office applications Knowledge of Lean manufacturing fundamentals FabrinetWest including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identify, age, disability, genetic

MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than 65 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. Click here to view our facilities. In addition, MACOM offers foundry services that represents a key core competency within our business. MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio. Quality Control Inspector 2 Job Description: Quality inspector must be a quick-thinking, self-motivated individual with knowledge on all aspects of inspection and testing. Able to generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers. Communicate non-conformance's and work with Quality, Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications. Job Qualifications: * 3-5 years QC inspection experience * Perform incoming inspection, in-process inspection, first article inspection and final inspection with little to no assistance * Read and Interpret piece part and assembly prints * Perform quality control inspections using a microscope and other quality tools such as micrometers, calipers, optical comparator and other measuring equipment * Complete, review and maintain acceptance documentation * Responsible for initial entry and assignment of non-conformance reports (NMRs) in quality database * Experience with Mil-PRF-38534, class H & K; Hybrids, Mil-STD-883; methods 2008, 2009, 2010, 2017 Semiconductors and Passive devices * Knowledge of IPC-600 & 610, J-STD-001 * Perform incoming inspection, in-process inspection, first article inspection and final inspection with little to no assistance (Required) * Handling ESD sensitive materials (Required) * Good communication skills are important, as well as the ability to explain findings clearly * Due to ITAR regulations, only candidates who are U.S. Persons (U.S. citizens, U.S. nationals, lawful permanent residents, or individuals granted asylum or refugee status) will be considered for this position. Other Special Skills: * Working knowledge of SAP, Agile, Excel, Word and Outlook * Good report writing skills are also useful. * Knowledge and experience in performing mechanical and electronic inspection The Salary Range for this position is $24 - $27 per hour. Actual salary offered to candidate will depend on several factors, including but not limited to, work location, relevant candidates' experience, education, and specific knowledge, skills, and abilities. EEO: MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, genetic information, veteran status, military service, marital status, or any other category protected under applicable law. Reasonable Accommodation: MACOM is committed to working with and providing reasonable accommodations to qualified individuals with physical and mental disabilities. If you have a disability and are in need of a reasonable accommodation with respect to any part of the application process please call *************** or email HR_*************. Provide your name, phone number and the position title and location in which you are interested, and nature of accommodation needed, and we will get back to you. We also work with current employees who request or need reasonable accommodation in order to perform the essential functions of their jobs.

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position Nurix Therapeutics is seeking a talented scientist to join the Analytical Development and Quality Control group. This role supports analytical and QC activities from clinical to commercial CMC development and manufacturing. The ideal candidate will have a strong background in analytical chemistry, with expertise in operating and troubleshooting HPLC and dissolution methods, as well as instrumentation for characterizing drug products. Experience with method development, method validation, and data interpretation is highly desirable. This position involves conducting method development and troubleshooting activities internally, as well as overseeing method development, validation, and testing at external CDMO/CRO partners. The Scientist will work closely with other departments to ensure seamless integration of analytical and QC activities. This position is based at Nurix headquarters in San Francisco, CA. Key responsibilities Design and conduct complex analytical experiments with consistency across several analytical platforms while employing appropriate controls. Manage method development, method validation, QC testing, and reference standard management activities internally and at CDMOs/CTLs. Perform laboratory-based experiments to optimize drug product analytical methods. Conducts complex experimental troubleshooting. Process, evaluate, and interpret experimental data, drawing conclusions based on results. Maintain detailed laboratory notebooks accurately. Present data at team and cross-functional meetings. Critical review of data, protocols, reports, specifications, and other documentation. Trending stability data and establishing retest periods/shelf life using statistical methods. Works collaboratively, cross-functionally, and within the team to achieve program goals. Travel up to 10%. Additional responsibilities as required. Qualifications Advanced degree in a relevant discipline (Chemistry, Pharmaceutics, or related field). BS degree with 10+ years, MS degree with 6+ years, or Ph.D. with 2+ years of industrial CMC experience. Expertise in HPLC and dissolution method development is essential. Experience in analytical method development and validation. Experience managing stability programs, reference standards, and retest/expiry. Familiarity with ICH guidelines, cGMPs, and pharmacopeial chapters. Ability to critically interpret data and articulate technical concepts in multidisciplinary settings. Ability to ensure assigned activities are completed to the satisfaction of project timelines. Strong interpersonal skills that foster collaboration within and outside of the organization. Ability to travel domestically and internationally. Fit with Nurix Culture and Values Strong team orientation; highly collaborative Solutions and results-oriented focus Hands-on approach; resourceful and open to diverse points of view Application Process Nurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US. Note to Employment Agencies: Please do not forward any agency resumes. Nurix will not be responsible for fees related to unsolicited resumes. Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy (*****************************************

Genefab is seeking an experienced analyst to join it's Quality Control Analytical group. In this role, you will support the GMP QC testing at GeneFab, with a focus on testing, method transfer, qualification, troubleshooting and investigations. ResponsibilitiesProvide technical expertise (SME).Provide technical support to Analytical Development and QC Analytical Operations as needed.Develop, implement, and update all Quality Control SOPs, testing records and other documentation needed for cGMP compliance. Perform QC testing on in-process and final product samples to support release and stability testing.Lead and perform technical root-cause investigations for aberrant results and deviations relating to analytical methods.Lead and train junior employees to ensure testing procedures and practices comply with all applicable regulations and procedures.Plan, lead, and execute analytical method transfers, qualifications, and validations. Draft, Review, and Approve Method Transfer Protocols and ReportsGenerate and review procedures, protocols and reports.Proactively identify areas for continuous improvement in processes and procedures and lead these initiatives.Collaborate closely with Interdepartmental MSAT, ASAT, and Manufacturing groups to support, execute, and/or provide oversight in the execution of method optimization, characterization, troubleshooting, transfer, and qualification Perform additional duties as assigned RequirementsB.S. degree in biology or related field with experience in cell therapy, immunology, cancer biology, or a closely related field.Minimum of 5+ years of GMP/QC Laboratory experience.Demonstrated ability to collaborate and work in cross-functional teams.Strong organizational skills and attention to detail Strong time management skills with a proven ability to meet deadlines Strong analytical and problem-solving skills Experience with relevant technologies such as: multicolor flow cytometry, cell culture (e.g., aseptic techniques, cell line expansion), multiplexed immunoassay, qPCR, and dPCR methods, Luminex, and ELISA. Experience in GMP.Experience with contract laboratories and or CDMO is a plus Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook record keeping (ELN) is a plus Proficient in MS Word, Excel, Project, and PowerPoint Experience with cell therapy or gene therapy is a plus Availability to work extended hours such as evenings or weekends to meet deadlines when necessary Comfortable in a fast-paced environment with minimal direction and able to adjust workload based on changing priorities Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the initial job description Able to lift up to 40 pounds $45 - $55 an hour About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.

Work Schedule Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Description Location/Division Specific Information: Sunnyvale, CA Second Shift: Monday - Friday 2:00PM to 10:30 PM with overtime and weekend hours as needed As part of the Chromatography and Mass Spectrometry Division (CMD), the Sunnyvale, CA site focuses on developing and delivering the highest quality chromatography solutions in the industry. How Will You Make an Impact?:Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables.A Day in the Life: Testing of resin products on unique instruments to meet customer demand. Record and report test results accurately and maintain proper documentation. Complete production work-orders according to established procedures. Follow corporate quality policy to ensure high-quality standards. Follow safety requirements and actively participate in safety improvement activities! Maintain a clean and organized laboratory environment. Education: High school diploma or equivalent required. Experience: Required: Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Knowledge, Skills, Abilities: Knowledge of Good Laboratory and Manufacturing Practices and standards. Good mathematical, problem-solving, and organizational abilities. Excellent verbal and written skills Read and understand written procedures (SOPs) and follow verbal instructions. Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) PC literate and have experience with spreadsheet and database software. Knowledge of Chromatography software and chemistry experience a plus. Physical Requirements / Work Environment Lift and/or move up to 40 pounds. Regularly required to sit, stand; walk; use hands & fingers to handle & feel. Visual abilities to detect small components and particles. Exposure to toxic or caustic chemicals, fumes or airborne particles. Occasionally exposed to moving mechanical parts and moderate noise level. PPE requirements: lab coat, Safety glasses, gloves, face shields, & safety shoes (all company provided.) P95 Mask in the areas that have exposure of solvent fumes Compensation and Benefits The hourly pay range estimated for this position based in California is $21.42-$32.13. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Why Ascend? Come work for a company that is transforming the industry! We are Eurofins Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment. Job Summary The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing. Responsibilities: Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens Instrument daily, weekly, and monthly maintenance Troubleshooting instruments Instrument validation Attends and completes advance training for department instrumentations Capable of assisting in sample processing and preparation in high complex test environments Actively participates in facility's Quality Assurance program Assists in orientation and training of new staff members, as directed by management Assumes responsibility for special projects, as directed by management Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed Qualifications: College degree, science related preferred or equivalent number of years of relevant job experience 2-4 years of experience Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely Compensation: $25-35/hr Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role Benefits: As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Eurofins Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law. The company's policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status.

Job Description FirstCarbon Solutions (FCS), an ADEC Innovation, is focused on improving the world we live in. It's our goal to improve the lives of all the people we work with, whether they are clients, partners, or colleagues. Come join our team of amazing professionals dedicated to making the world a better place! An Air Quality Scientist (CG04) prepares technically sound and legally defensive air quality, greenhouse gas, and energy analyses and technical appendices, primarily for California Environmental Quality Act (CEQA) and National Environmental Policy Act (NEPA) documents, such as Initial Studies (ISs), Environmental Analyses (EAs), Environmental Impact Reports (EIRs) or Environmental Impact Statements (EISs). This role is approximately 85% report writing/analysis and 15% modeling, this role is an on-call or part-time role that can advance to a full time position. Duties and Responsibilities Provide support and assistance to Section and Project Managers in research, technical writing, and model/simulation functions, as requested, as well as provide recommendations to improve efficiency and effectiveness Develop technically and legally defensible air quality, greenhouse gas, and energy analyses and technical appendices to be included in CEQA and NEPA environmental documents Use approved software models, such as the California Emissions Estimation Model (CalEEMod) and EMFAC, to estimate a project's air pollutant emissions Develop and quantify the emission reduction potential of appropriate mitigation measures, if needed Develop either technical reports or sections for environmental documents Use air dispersion models, such as AERMOD and HARP, to evaluate the project's construction-related and operational-related emission and health impacts Develop air quality policy documents, such as air quality elements to General Plans Help develop mitigation monitoring plans and programs to ensure compliance with stated and agreed-to mitigation requirements Meet the firm's and client's goals within the agreed-upon scope of work and budget Develop and maintain mutually beneficial relationships with clients and colleagues Represent and promote the firm's strengths/reputation in the air quality industry Skills Ability to plan, organize, and coordinate air quality assessments Provide effective and quality communication through written and oral methods Work creatively as a member of an environmental assessment team Promote teamwork through interpersonal skills Marketing and proposal preparation Demonstrated proficiency in MS Office applications, especially Word and Excel, as well as internet usage Education and Experience Bachelor’s degree in environmental sciences or related field required; Master's degree in Environmental Management or equivalent a plus 2-4 years of experience in Environmental Services, air quality and/or greenhouse gas emission inventory quantification, and modeling skills, including AERMOD, CalEEMod, ArcGIS, and other software models Other air permitting or assessment/modeling experiences are highly desired Work Environment The position operates in a remote, home office environment. This role routinely uses standard office equipment. This position may require some travel to attend meetings as well as fieldwork. This role may be exposed to a variety of terrains and a variety of weather conditions while performing fieldwork. Physical Demands While performing the duties of this job, the employee is regularly required to talk and listen. The employee may spend extended periods of time sitting in front of the computer. The employee must stand, stoop, walk, and reach with hands and arms and hand/finger dexterity. Specific vision abilities this job requires include close vision, distance vision, and the ability to adjust focus. Salary: $60,000 - $72,500 FCS offers competitive salaries and robust benefits with opportunities for personal and professional development. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply! Competitive, progressive benefits including Remote/Hybrid/in-office work location options Escalating PTO structure Up to 10 paid holidays (up to 4 are flexible holidays) Full health care package: Up to 100% employer-paid employee medical and 55% eligible dependent coverage* 80% employer-paid dental and vision Employer-paid Life and AD&D insurance Short- and long-term Disability insurance Employee Assistance & Wellness Program 401k & Roth Pet insurance discounts Information Security Adhering to all policies, guidelines, and procedures pertaining to the protection of information of the organization, employees must maintain confidentiality of all sensitive information to which they are given access. They are also responsible for reporting actual or suspected events or incidents, including vulnerabilities or breaches, that may affect the confidentiality, integrity, and availability of information to members of the Management Team. Mutual respect is fundamental. Fundamental to our teams. Fundamental to our clients. Fundamental to the communities we serve and live in. Fundamental to the landscapes we work within. We need you and your unique talents, history, and background to become the Company we aspire to be. We insist upon a culture of common respect, expect transparency, and celebrate the fundamental value and dignity of all individuals. Our mutual equality as humans is the path to innovative collaboration. We cultivate integrity, driving us to growth, and allowing us to achieve more together than we could ever hope to as individuals.

The Bed Control Coordinator insures the effective and efficient utilization of acute and long-term care beds, and hospital resources as well as insuring proper registration procedures are followed. This position acts as a liaison between physician, department managers, patients and external agencies concerning the admitting process and is responsible for maintaining the confidentiality of all patient information. Responsibilities POSITION SPECIFIC DUTIES (other duties may be assigned) Assumes responsibility for position responsibilities outlined in the Registrar job description. Maintains the hospital census and reconciliation with nursing units. Calculate observation hours and enter on the account. Reports direct admissions to the nursing supervisor who determines medical necessity and appropriate level of care; coordinates effective patient flow to insure internal and external customer satisfaction; informs physicians of patient arrival times; coordinates admissions with nursing units, ambulances and external entities. Evaluates patient financial status at admission and/or referring to the Patient Financial Advisor as appropriate. Secures and releases patient valuables at admission and discharge. Prepares all surgery and/or GI packets for the following day securing patient orders, insurance verifications and patient notification of possible out of pockets. Completes additional projects as requested by Supervisor or Director. Takes initiative and performs as self-starter in daily activities. Qualifications QUALIFICATIONS/JOB REQUIREMENTS: EXPERIENCE: One year of patient registration experience in an acute facility. More years of experience may be required if hired in a registration area that demands more experience. Work in a physician's office may be substituted for an acute hospital setting if duties are similar. OTHER SKILLS, ABILITIES & KNOWLEDGE: Understands the registration process, managed care/capitation, Medi‑Cal, Medicare regulations, Medical Terminology, HIPAA, ABN, and EMTALA regulations Works effectively with the public, physicians, and staff Provides quality customer service including enhancing patient satisfaction while possessing the ability to work in a high volume production‑oriented and structured environment

Pay: $21.00 $24.00/hr. | Paid Weekly Schedule: TuesdayFriday and the second Saturday of every month Hours: 7:00 AM until finish (typically 1012 hour days) Work Environment: In Field Who We Are Honey Bucket, a division of Northwest Cascade, is changing expectations by providing exceptional portable sanitation and site services in our community. With over 750 employees across seven states, our team exceeds customer expectations in portable restrooms and services, hand-washing stations, fencing, and storage containers. Were an employee-owned company that provides under-credentialed overachievers an opportunity to earn more than just a paycheck. What Youll Do A Day in the Life As a Quality Control Inspector, you'll be out in the field ensuring our units meet high standards before and after service. Your day will include: * Driving a designated route and inspecting 4060 units per day * Submitting electronic inspection reports with detailed notes * Communicating results to the Quality Control management team * Representing Honey Buckets commitment to quality and customer satisfaction What You Bring Were looking for someone who is: * Detail-oriented You notice what others miss * Tech-comfortable Able to learn and use mobile/inspection software * Reliable Ready to work a full route each day * Communicative Clear in both written and verbal communication * Team-focused Willing to take on extra tasks with a great attitude * Driving Record Must have a clean driving record and pass background check and drug test Why Honey Bucket? We invest in our people: * 100% employer-paid medical, dental, and vision * 401(k) with company match * Tuition reimbursement and learning opportunities * Annual performance bonuses * Paid time off (PTO) * Weekly pay and stable, year-round work Ownership and Advancement As an employee-owned company, we share profits and offer shareholder opportunities to management. We believe in promoting from within and helping our team members build long-term careers. Equal Opportunity Employer Northwest Cascade and Honey Bucket are proud Equal Opportunity Employers. We believe diverse ideas, perspectives, and backgrounds create a strong and innovative workforce. All applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. IND123

Quality Control Technician Get Hired Today! We have an excellent opportunity to work for a food company as a Quality Control Technician in Gilroy, CA! If you’re a detail-oriented person, this is the job for you! Grade finished products such as packaging, weighing, counting, and record data results. All other duties assigned by the supervisor. Quality Assurance, you will be walking to many different parts of the facility to take samples and measurements of product. You will use the lab to run tests on the samples and product you pull. You will complete timely reports of your samples. Computer usage and other technology may be required. Be prepared to be crossed trained in different tasks and departments that accommodate production needs. Apply Today! Pay: $18.50-$18.75/hr. Why work for Advance Services, Inc. Advance Services is for and about people; we are your employment specialists. Enjoy our easy application process. You NEVER pay a fee! Weekly pay. Fun Safety and attendance incentives. Health Benefits to keep you and your family healthy. Great Referral Incentives. Advance Services partners with the top companies in the area! Apply for this job by clicking the apply button. You will be directed to our website, *********************** Please select a branch near you or call our office at ************ Stop in and see our experienced, bilingual, and friendly staff today at 8021 Kern Ave., Gilroy, CA 95020 Advance Services is an equal opportunity employer #429

What you'll do Lilac is seeking a chemical technician, chemistry student or chemical engineering student to be involved in the development and scale-up of Lilac's evaporation, crystallization, purification, and other related operations for the production of battery grade lithium products. The successful candidate will be involved with the testing and production of battery grade lithium carbonate in the Lilac laboratory facilities. This hands-on role includes equipment setup and operations of the test equipment to evaporate, crystallize, and filter final product. The candidate will work under the guidance of the Lilac crystallization specialist, and work with the chemistry team to ensure sampling and chemistry analytical work adheres to requirements. The term of engagement is about 2-months with the possibility of extension or a permanent role. Qualifications Candidates must have at least 6-months hands on lab experience or be majoring in Chemistry or a related discipline. Familiarity with ICP-OES, Titrations, and PSA is preferred. Candidates must be authorized to work in the US on a full-time indefinite basis without the need for sponsorship now or later. Excellent communication skills and ability to interface and collaborate with other engineers, chemists, and operators Excited to work on a small fast-paced startup team with a drive to succeed and grow with the company EEO Statement Lilac Solutions is committed to providing a professional work environment free from discrimination and harassment, including discrimination and harassment based on a protected category, and an environment free from retaliation for participating in any protected activity. Lilac Solutions is committed to providing equal employment opportunities to all employees and applicants for employment. A Note to Third-Party Recruiters At this time, we are not accepting unsolicited resumes from non-partnered third-party recruiters or staffing agencies. Resumes sent without prior arrangement will be considered the property of Lilac Solutions, and no fees will be paid if we hire a candidate whose resume was submitted unsolicited.

Ultimate Staffing is seeking an R&D Technician to join a client in San Jose. This is a long term contract position. Hours for the role are Monday - Friday 9:00 am - 5:30 pm. Job Responsibilities: Follow all safety protocols while working closely with scientists and engineers to support experimental research activities. Operate automated equipment to build proprietary devices in accordance with standard operating procedures (SOPs) or under the guidance of an engineer. Utilize metrology tools and assist with routine lab tasks to support process development and tool optimization. Maintain accurate records of daily experiments and report progress using Microsoft Office tools. Identify and communicate any irregularities or unexpected outcomes to the appropriate team members. Minimum Qualifications: High school diploma or equivalent with a minimum of 3 years' experience in an R&D lab environment. Strong attention to detail and a commitment to producing high-quality results. Proficiency in basic computer applications, including Microsoft Office and internet browsers. Preferred Qualifications: Comfortable working in a fast-paced, evolving research environment. Willingness and ability to learn a variety of laboratory techniques. Flexible, team-oriented mindset with the ability to collaborate across multiple projects. Familiarity with using software tools to complete tasks and document data. Physical Requirements: Must be able to work in a dry room environment. 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.

Shift: 3rd shift, graveyard (shift begins: 10pm) Performs a variety of inspection procedures to ensure quality levels at various stages of manufacturing at or above the standard. Support the organization goals in achieving total customer satisfaction. Key Responsibilities: * Inspect in-process or finished production assemblies and sub-assemblies for conformance to quality assurance standards * Working from blueprint, engineering change notices, or established operating procedures determine acceptance or rejection or rework requirements of a part * May evaluate new procedures for non-standard rest and perform special set-up on new equipment * Assist others in correcting or preventing deficiencies in quality or workmanship * Give work direction to other inspectors * Know your customers' expectations and drive action to meet them * Perform first article process * Identify component * Perform related work as assigned Job Qualifications: Education: Secondary/High School, Certificate Diploma Experience: 6+ Years preferably in Quality a plus Required skill: * PCBA Experienced * Able to use measurement equipment. * Must be able to read ECO/Dev instruction/build drawer and BOM. * Familiar with SMT and identify component, IPC 610 Knowledge and preferred IPC Cert. Familiar w/ First Piece and First Article process. Job Competencies: * Attention to detail * Communication skills - verbal and written * Organized and good critical thinking skills * Data collection, management and analysis * Team work * Ability to interpret complex customer rules and regulations * Demonstrated skills in project management and ability to train others to lead projects * Works well independently * Excellent interpersonal and communication skills * Ability to manage time and prioritize multiple task in a fast paced environment * Proficient in use of MS Office applications * Knowledge of Lean manufacturing fundamentals FabrinetWest including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identify, age, disability, genetic Posted On: Wednesday, June 11, 2025 Compensation: $20-$23/hour

Job Description Chemistry Lab Analyst Why Ascend? Come work for a company that is transforming the industry! We are Eurofins Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment. Job Summary The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing. Responsibilities: Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens Instrument daily, weekly, and monthly maintenance Troubleshooting instruments Instrument validation Attends and completes advance training for department instrumentations Capable of assisting in sample processing and preparation in high complex test environments Actively participates in facility's Quality Assurance program Assists in orientation and training of new staff members, as directed by management Assumes responsibility for special projects, as directed by management Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed Qualifications: College degree, science related preferred or equivalent number of years of relevant job experience 2-4 years of experience Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely Compensation: $25-35/hr Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role Benefits: As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Eurofins Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law. The company’s policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status. Powered by JazzHR t09VLs1XEi