Quality control analyst jobs in Gilroy, CA - 139 jobs

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. The "Fine Print" - What You'll Do Execute GMP-compliant testing of cell therapy products and in-process samples, with a focus on molecular assays (dd PCR, qPCR), flow cytometry, and functional assays for CAR-T cells. Perform cell culture and expansion of engineered T cells, maintaining aseptic technique and quality standards. Contribute to drafting and updating SOPs, forms, and logbooks governing lab operations, equipment maintenance, and assay procedures. Coordinate preventive maintenance, calibration, and troubleshooting of lab equipment and instruments in collaboration with internal resources and external partners. Manage inventory of cell culture reagents, molecular assay supplies, and lab materials. Support GMP investigations, including out-of-specification results, assay deviations, invalid assays, change controls, and CAPAs, with a focus on molecular and functional testing. Assist in tracking, trending, and reporting QC data for molecular assays, cell culture, and CAR-T functional studies. Skills And Experience We Look For BS or MS in Biological Sciences, Immunology, or a related field. 2+ years in pharmaceutical or biotechnology industry, including cell therapy/CAR-T experience. Hands-on experience with molecular assays and flow cytometry. Experience in cell culture and performing CAR-T functional assays. Familiarity with GMP-compliant lab practices and QC data tracking. Excellent written and oral communication skills. Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $80,000 - $105,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Medical Device R&D Technician Pay $35-38 6 month+ assignment Onsite in Campbell, CA Assemble fluidic tube sets, mechanical gear, and catheter-based devices in a clean room environment through adhesive bonding and cure, mechatronic assembly and electrical/mechanical testing. Demonstrated history of working on complex mechanical and electrical systems. • HS diploma and a minimum of 8 years related experience; AA degree and a minimum of 5 years experience preferred. • Strong understanding of assembly and calibration methods. • A proven ability to work well in a team environment • Must be capable of working independently and in a team while being flexible and self-motivated. • Previous experience assembling Medical Devices in an FDA-regulated environment is preferred. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Assemble complex mechanical systems that encompass hundreds of unique parts. Your expertise with precision tools will ensure the accurate placement of linear guides, rotary bearings, actuators, motors, and drive systems. • Collaborate closely with engineers to develop work instructions, maintain inventory for development builds, and ensure a clean and organized build environment. • Maintain and calibrate tools, replenish stock fasteners, and ensure organization in the development and build areas. • Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy. • Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, and applicable FDA and Regulatory requirements. • Actively promote and support the company's Management Review process. • Inform responsible personnel of concerns involving product quality. Benefits (employee contribution): Health insurance Health savings account Dental insurance Vision insurance Flexible spending accounts Life insurance Retirement plan All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

TITLE: CHEMICAL TECHNICIAN FLSA STATUS: NON-EXEMPT D SHIFT: FRIDAY THRU SUNDAY AND EVERY OTHER THURSDAY 6:00 PM TO 6:00 AM REPORTS TO: PRODUCTION SUPERVISOR Under the direction of the Production Supervisor, the Chemical Technician is responsible for the routine changing of solvents, etch tank fluids, and resist bottles; making, pouring, and maintaining develop solution and lapping slurries; performing tests using various laboratory tools and analyzing the results to ensure consistency; and disposing of chemical waste as needed. This position is located in Milpitas, California. *Must be willing to train on F Shift (Friday thru Sunday and every other Thursday 12:00 PM-12:00 AM) for a minimum of two months before moving to assigned shift. ESSENTIAL FUNCTIONS: Performs routine changing of solvents, etch tanks fluids, and resist bottles to ensure a ready supply of fresh chemicals Prepares, pours, and maintains various chemicals, developing solutions, and etch slurries Manages, monitors, and stocks chemical supplies; informs Materials department when inventory is low or needs to be replenished Performs routine chemical testing to ensure consistency of products using various laboratory tools; analyzes results and reports deviations Properly disposes of chemicals to ensure compliance with Environmental Health and Safety requirements Responds to chemical spills quickly and according to established procedures; participates in the Headway Spill Response team Responds to inquiries from other team members, managers, or departments Overtime may be required contingent on business need Adheres to all safety policies and procedures as required Performs other duties of a similar nature or level* MINIMUM QUALIFICATIONS: High School or General Education Diploma (GED) Experience working in a semiconductor or high volume manufacturing environment or similar industry Experience working with and disposing of chemicals, solvents, or similar compounds Proficient in the use of Microsoft Office Applications Knowledge, Skills, and Abilities: Knowledge and ability to handle, maintain, and properly dispose of hazardous chemicals, solvents, or similar compounds Knowledge and ability to use basic analytical tools to test chemicals for consistency and quality Knowledge and ability to use Microsoft Office applications to create spreadsheets, Word documents, and presentations Ability to follow written or verbal instructions regarding appropriate chemical handling procedures Able to communicate effectively, both verbally and in writing, with all levels of consultants, employees, management, and vendors Able to work productively and collaboratively with all levels of employees and management Able to comply with all safety policies and procedures Able to comply with all clean room protocols and procedures for handling hazardous chemicals Demonstrated ability to resolve equipment maintenance issues quickly and efficiently Demonstrated organizational and time management skills Demonstrated problem-solving and trouble shooting skills Flexible and able to prioritize The hourly rate for this full-time position is between $22.00-$35.00+ bonus target + benefits. Within the range the individual pay may differ depending on additional factors including job responsibilities, job related knowledge, skills, abilities, education, and experience. The hourly pay range shown is subject to change and may be modified periodically. WORKING CONDITIONS: The Chemical Technician works in an indoor environment on a rotating schedule on D shift which is Friday thru Sunday and every other Thursday from 6:00 PM to 6:00 AM. The work hours may be altered from time-to-time contingent on business needs. Technician works in a class 100 ESD sensitive wafer fab manufacturing facility; adheres to OHSA required safety and dress standards. May travel from building-to-building as needed. Technician may be subject to high noise levels, hazardous chemicals, and particulate matter from time-to-time; must be clean-shaved in order to wear a respirator when required. Stands and walks; performs various fine grasping movements, bends, kneels, crawls, and twists; operates a computer and enters information using a keyboard, operates a telephone, and other office equipment; must be able to push, pull, lift, or carry above the waist up to 75 pounds. *Other duties of a similar nature or level are duties that may be required, but may not be specifically listed in the job description or posting. TDK/Headway Technologies, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, national origin, age, disability, or genetics. Applicants requiring accommodation in order to complete the application process should contact the Headway Human Resources Department.

Job DescriptionQC Technician (Salinas/Yuma) Duda Farm Fresh Foods, Inc. is seeking a Quality Control (QC) Technician for an immediate opening. This role is responsible for ensuring that all incoming products meet USDA standards, DFFF requirements, and customer specifications. The position reports directly to the National QC Manager and will be based in Salinas, CA and Yuma, AZ. Essential Job Responsibilities Inspect all loads arriving at the facility-whether from the field or purchased-to ensure finished, packed commodities meet USDA, DFFF, and/or customer-specific specifications. Periodic field-level inspections may be required. Report any issues in real time to the appropriate management. Verify PTI labels and pallet license plates for product description, legibility, and accurate best-by/use-by dates. Perform daily temperature checks on on-hand commodity inventory to ensure proper temperature maintenance. Complete bi-weekly age reports (Monday and Thursday) on inventory to confirm quality and food safety standards. Immediately report any deviations, such as rapid quality loss or compromised product. Submit inspection documents to the Manager for daily verification. Address all deviations in real time and ensure proper documentation and organized storage. Confirm that measuring devices (e.g., thermometers) are calibrated daily and maintain calibration records. Conduct food safety visual inspections during quality checks. Report any foreign material or concerns to Management immediately for corrective action. Ability to travel between growing regions to cooling facilities in Salinas, CA (April to November) & Yuma, AZ (November to March). Follow all safety work practices by following safety rules and regulations. Comply with all company policies and procedures. Must use all required PPE (Personal Protective Equipment). Must be able to work without directions and stay productive. Must be dependable, punctual, and able to work flexible hours as needed. Must be able to work weekends. Must be able to work overtime when requested. Other duties as assigned. Required Knowledge Skills and Abilities: High School diploma required Bilingual preferred but not required. Agriculture or demonstrated interest in agriculture preferred Valid CA driver's license Basic knowledge of Microsoft Word, Outlook and Excel preferred. Working Conditions: Working environment will include warehouse, cold room and/or field. Works well on own and in a team environment. Must be willing to work outside of normal business hours (8:00AM-5:00PM) and weekends when necessary. Ability to perform physical labor, including lifting up to 65 lbs. and working in outdoor environments. Regular climbing, stooping and bending required. Overnight travel may be required. Benefits: 401(k) 401(k) matching Dental insurance Disability insurance Employee assistance program Flexible spending account Health insurance Life insurance Paid sick time. Paid time off Vision insurance Job Type: Full-time Pay: $25.00 Duda Farm Fresh Foods provides a fair and equal employment opportunity for all employees and job applicants regardless of race, color, religion, national origin, gender, sexual orientation, age, marital status or disability. We expect and require the cooperation of all employees in maintaining a discrimination and harassment-free work environment. We offer an excellent benefit package as part of our total compensation including medical, dental and vision insurance, 401K, flexible spending accounts, tuition reimbursement program, paid time off and much more. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Due to the high volume of applications received, only those candidates who are selected for interviews will be contacted. Powered by JazzHR KsEiEJDiK6

The Opportunity We are seeking a QC Analytical Associate Manager to lead and oversee quality control laboratory operations. This role involves managing analytical testing, ensuring compliance with industry standards, and driving continuous improvement initiatives. The ideal candidate will have experience in analytical or cleanroom-based labs, strong leadership skills, and a results-driven approach. What You'll Do: Safety & Compliance: Address and resolve EH&S concerns in collaboration with the QC Manager and Team Lead. Ensure compliance with internal inspection findings. Tool & Equipment Management: Oversee tool downtime responses, business continuity planning (BCP), and coordination with planning, logistics, and sales teams. Strategic Planning & Budgeting: Develop QC Analytical group goals and projects with the QC Manager. Manage department budgets and resource allocation. KPI Management & Continuous Improvement: Monitor and optimize QC analytical test and tool KPIs; oversee improvement initiatives where feasible. Project Oversight: Ensure tool qualification and project execution within budget, quality, and timeline constraints. Performance & Development: Provide structured feedback on engineers' performance and competency assessments. Operational Support: Act as a backup for the QC Analytical Lead, assisting in testing, process control systems, audit preparations, and personnel training. Customer & Technical Requirements: Maintain a working understanding of customer specifications and ensure alignment with current metrology capabilities. Problem-Solving & Risk Management: Promote the use of troubleshooting methodologies (e.g., fishbone diagrams, 8D, DOEs) and risk management tools. Perform other duties as assigned. What you Bring: Minimum BS/MS degree in Chemistry, Materials Science, Chemical Engineering, Mechanical Engineering, Electrical Engineering, or Industrial Engineering. At least 2 years of leadership or supervisory experience in an analytical or cleanroom-based lab (e.g., trace metals lab). Proficiency in GLPs, ISO standards, SQC/SPC principles, cleanroom protocols, and general safety practices. Experience with LIMS, XML, and JMP is a strong plus. Strong communication and interpersonal skills, with the ability to multitask in a fast-paced environment. Experience in department budgeting, manpower planning, tool utilization, and KPI monitoring; improvement execution is a plus. Solid background in third-party and customer audits. Ability to lead discussions and cross-functional projects within and outside the department. Familiarity with company employment policies and practices. Your Core Strengths: Communication & Interpersonal Skills - Ability to collaborate effectively across teams. Leadership & People Development - Strong mentoring and team management abilities. Decision-Making & Problem-Solving - Analytical approach to challenges and improvements. Business Acumen & Results Orientation - Focused on achieving strategic and operational goals. Why Join Us? Work in a cutting-edge lab environment where quality and precision matter. Lead and grow a high-performing QC team in a dynamic, fast-paced industry. Be part of a company that values innovation, leadership, and continuous improvement. Enjoy opportunities for career advancement, professional development, and cross-functional collaboration. If you're ready to take your QC leadership skills to the next level and drive excellence in analytical quality control, apply today! Exact compensation may vary based on skills, experience, and location. (Salary Range - $116,000/yr to $160,000/yr) JSR is an Equal Employment Opportunity and Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. **Recruitment agencies/Headhunter do not submit resumes/CVs through our Web site or directly to managers. JSR will not pay fees to any third-party agency or company that does not have a signed agreement with JSR. JSR do not accept unsolicited headhunter and agency resume.** #jsrmicro

FQC (Final Quality Control) San Jose, CA About the job: FULL-TIME/TEMPORARY (POSSIBILITY FOR PERMANENT) About the JobFoxconn Industrial Internet (Fii), is a world leading professional design and manufacturing service provider of communication network equipment, cloud service equipment, precision tools and industrial robots. FII provides customers with intelligent manufacturing services for new forms of electronic equipment products centered on the Industrial Internet platform. As a FQC you will be mainly responsible for testing materials and finished products to ensure they conform to all applicable laws and company standards. Quality Control Technicians test products across the three stages of production (before, in-process, and final) to ensure quality levels are met. QUALIFICATIONS: EDUCATION: High school diploma or GED equivalent and/or training or equivalent combination of education and experience EXPERIENCE: Minimum of 1-2 years of experience in a manufacturing environment LANGUAGE: English proficiency is required, Mandarin proficiency is a plus. SKILLS: Great verbal and written communication skills Familiarity with electronic and mechanical components related to PCBA contract manufacturing Accuracy for documentation Effectively present information and respond to questions from managers and employees Common sense to solve practical problems Knowledge of ESD, IPC-600/610, workmanship standards and experience Attention to detail RESPONSIBILITIES: Use basic inspection tool/device, example: magnifying lens, microscope, caliper, and color pantone Maintains safe and clean working environment by complying with procedures, rules, and regulations Inspect materials or assembled parts or products for defects and deviations from specifications Observe and monitor production operations and equipment to ensure conformance to specifications and make or order necessary process or assembly adjustments Discuss inspection results with those responsible for products Discard or reject products, materials, and equipment not meeting specifications Contributes to team effort by accomplishing related results as needed Develop and maintain inspection reports Ensure compliance to federal and state laws, as well as company standards and specifications Maintain calibration of quality control equipment Perform inspections across all stages of of production Prepare and maintain test data for review Evaluate data and draft reports, noting any relevant deviations from existing standards Identify areas for quality control improvement and implement new methods accordingly Communicate quality or compliance concerns with urgency Pay rate: $22/h Status: Non-Exempt Work schedule: Swing shift: 3:15PM - 11:45PM Foxconn Assembly, LLC is an Equal Opportunity Employer (EOE). All qualified candidates will receive consideration without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or marital status in accordance with applicable federal, state and local laws. Foxconn Assembly, LLC participates in E-Verify and will provide the federal government with your Form I- 9 information to confirm that you are authorized to work in the U.S.

1X Since its founding in 2015, 1X has been at the forefront of developing advanced humanoid robots designed for household use. Our mission is to create an abundant supply of labor through safe, intelligent humanoids. We strive for excellence in all we do, solving some of the hardest problems in robotics with the world's most talented individuals. Every part of our robots is designed and produced in house, from motor coils to AI, reflecting our vertically integrated approach. At 1X, you will own real projects, be recognized for your achievements, and be rewarded based on merit. We are seeking a Lab Chemistry Technician who is passionate about hands-on experimentation and eager to support the creation of advanced materials for next generation humanoid robots. This role is ideal for someone who enjoys preparing materials with precision, running characterization tests, executing polymer and other organic synthesis reactions, and working closely with senior scientists in a fast paced laboratory environment. You will work directly under the supervision of the Polymer Chemist and the Materials Science Lead, supporting the development of elastomers, coatings, adhesives, textiles and multilayer material systems that enable future robot architectures. Key Responsibilities Prepare polymer formulations, elastomers, textiles and composite samples, and perform hands-on laboratory experiments including the synthesis and modification of polymers under senior scientist supervision. Operate laboratory equipment for mixing, curing, casting, coating, laminating, and other processing of soft material systems. Execute and improve synthesis workflows using glass and stainless reactors, feed pumps, temperature controllers, nitrogen purging systems, and filtration equipment, following SOPs for start up, shut down, and cleaning. Conduct material characterization such as tensile testing, hardness measurements, rheology, thermal analysis, adhesion testing, and visual inspection. Maintain meticulous laboratory records, document procedures and results, and contribute to technical reports when required. Communicate results, observations, and interpretations clearly and proactively to supervising scientists. Maintain an up to date SDS database and ensure proper labeling, handling, storage, and inventory management of chemicals and materials. Perform all work in a safe and responsible manner, follow established safety procedures, and contribute to ongoing improvements in lab safety practices and workflows. Uphold strict confidentiality and maintain awareness of intellectual property responsibilities. Assist in building small scale prototypes, participate in pilot processing trials, and support rapid iteration across multiple experiments. Help maintain an organized laboratory environment that supports efficient workflow, safety compliance, and reliable daily operations. Work effectively within a diverse team, demonstrating initiative, accountability, and steady progress toward objectives and milestones. Job requirements Required Qualifications At least a two year degree in chemistry, chemical engineering, biochemistry, materials science, or a related field. Scientific knowledge and the ability to understand and carry out standard laboratory methods with accuracy and care. Experience performing a wide range of research experiments and tests, including setup and operation of laboratory apparatus and equipment. Ability to operate synthesis and processing equipment including glass and stainless reactors, feed pumps, temperature controllers, nitrogen purging systems, and filtration setups. Hands on experience preparing samples, handling chemicals, and working with laboratory tools in a safe and organized manner. Familiarity with mixing, curing, casting, coating, or testing of polymers, elastomers, or composite materials is a plus. Strong attention to detail and ability to follow precise procedures and documentation standards. Comfort working with scientists, engineers, and cross functional teams in a fast moving research environment. Eagerness to learn new techniques, operate new equipment, and support diverse experiments. Strong organizational skills, reliability, and clear communication. Location Policy We believe the best work is done when collaborating and therefore require in-person presence in our office locations. On-site Palo Alto, California, United States $54,000 - $100,000 per year Hardware EngineeringAll done! Your application has been successfully submitted! Other jobs

Job Description FQC (Final Quality Control) San Jose, CA About the job: FULL-TIME/TEMPORARY (POSSIBILITY FOR PERMANENT) About the JobFoxconn Industrial Internet (Fii), is a world leading professional design and manufacturing service provider of communication network equipment, cloud service equipment, precision tools and industrial robots. FII provides customers with intelligent manufacturing services for new forms of electronic equipment products centered on the Industrial Internet platform. As a FQC you will be mainly responsible for testing materials and finished products to ensure they conform to all applicable laws and company standards. Quality Control Technicians test products across the three stages of production (before, in-process, and final) to ensure quality levels are met. QUALIFICATIONS: EDUCATION: High school diploma or GED equivalent and/or training or equivalent combination of education and experience EXPERIENCE: Minimum of 1-2 years of experience in a manufacturing environment LANGUAGE: English proficiency is required, Mandarin proficiency is a plus. SKILLS: Great verbal and written communication skills Familiarity with electronic and mechanical components related to PCBA contract manufacturing Accuracy for documentation Effectively present information and respond to questions from managers and employees Common sense to solve practical problems Knowledge of ESD, IPC-600/610, workmanship standards and experience Attention to detail RESPONSIBILITIES: Use basic inspection tool/device, example: magnifying lens, microscope, caliper, and color pantone Maintains safe and clean working environment by complying with procedures, rules, and regulations Inspect materials or assembled parts or products for defects and deviations from specifications Observe and monitor production operations and equipment to ensure conformance to specifications and make or order necessary process or assembly adjustments Discuss inspection results with those responsible for products Discard or reject products, materials, and equipment not meeting specifications Contributes to team effort by accomplishing related results as needed Develop and maintain inspection reports Ensure compliance to federal and state laws, as well as company standards and specifications Maintain calibration of quality control equipment Perform inspections across all stages of of production Prepare and maintain test data for review Evaluate data and draft reports, noting any relevant deviations from existing standards Identify areas for quality control improvement and implement new methods accordingly Communicate quality or compliance concerns with urgency Pay rate: $22/h Status: Non-Exempt Work schedule: Swing shift: 3:15PM - 11:45PM Foxconn Assembly, LLC is an Equal Opportunity Employer (EOE). All qualified candidates will receive consideration without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or marital status in accordance with applicable federal, state and local laws. Foxconn Assembly, LLC participates in E-Verify and will provide the federal government with your Form I- 9 information to confirm that you are authorized to work in the U.S. Powered by JazzHR vj Ac8GA8kM

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

Work Schedule Second Shift (Afternoons) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Description Location/Division Specific Information: Sunnyvale, CA Shift: Monday - Friday 2:00PM-10:30PM 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 What We Offer Compensation Competitive Hourly Pay Rate Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities Compensation and Benefits The hourly pay range estimated for this position based in California is $21.42-$27.00. 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: *****************************************************

Hourly Salary Range: $24.00-$25.00/hr Work Schedule: Day Shift (6:00 AM-2:30 PM) MINIMUM REQUIREMENTS: Prior Experience in Inspecting to IPC-610 Standards Basic Inspection Experience on Mechanical Assembly (Nuts, Screws, Washers, Wire Harness) Ability to read Assembly Drawings and Manufacturing Instructions Job Description/Responsibilities: PCBA inspection (defect detection) of Through-Hole and Mechanical Parts based on IPC-A-610 and Customer Requirements. Knowledge and understanding of Manufacturing Process Instructions, product documentation, and deviation implementation. Reporting any non-conformance/defects during the manufacturing process via DGS system (Venture's MES System). Responsible for accurately reporting yield data per the Post Wave QC Process. Conduct First Article Inspection process for Through-Hole and Mechanical Parts. Check component polarity, markings, orientation, height, and placement. Verify loaded components on the Printed Circuit Board prior to soldering process. Responsible for feedbacking any information to Process and Quality Engineering departments for process improvements. Responsible for any additional in-process inspection points determined by Quality Engineering. Job Requirements: High School Education or equivalent. Minimum two years of inspection experience following IPC-A-610 requirements of surface mount and through-hole technology for printed circuit board assemblies is a must. Ability to read and understand manufacturing work instructions Ability to pass in-house IPC-A-610 Test and Certification Program. Ability to read and understand Engineering Drawings and Component Datasheets is a must. Experience using calipers, micrometers, magnifier lamp, microscopes. Excellent written and verbal communication and interpersonal skills. Ability to interpret quality control specifications. Experience in contract manufacturing. Ability to communicate effectively with co-workers. Preferred but Not Required: IPC-A-610 CIS or CIT Certification through IPC Organization. J-STD-001 CIS or CIT Certification through IPC Organization. Experience in ISO13485 (Medical) and AS9100 (Aerospace) products is a plus. #EmploynetJobsFremont

Prepare chemical solutions and formulations based on standardized or experimental protocols. Conduct synthesis and blending of raw materials to create new or improved chemical products. Operate lab equipment such as mixers, reactors, pH meters, and viscometers. Perform stability, purity, and potency testing on formulations. Record detailed data in lab notebooks and digital systems. Assist in scaling formulations from lab to pilot or full production. Troubleshoot formulation issues and adjust component ratios as needed. Ensure all formulations meet safety, quality, and regulatory standards. Collaborate with chemists, engineers, and quality control teams. Maintain clean and safe lab environments, including proper handling of hazardous materials. Responsibilities * Prepare chemical solutions and formulations based on protocols. * Conduct synthesis and blending of raw materials for chemical products. * Operate lab equipment such as mixers, reactors, pH meters, and viscometers. * Perform stability, purity, and potency testing on formulations. * Record detailed data in lab notebooks and digital systems. * Assist in scaling formulations from lab to pilot or full production. * Troubleshoot formulation issues and adjust component ratios as needed. * Ensure formulations meet safety, quality, and regulatory standards. * Collaborate with chemists, engineers, and quality control teams. * Maintain clean and safe lab environments, handling hazardous materials properly. Essential Skills * Bachelor's degree in Chemistry, Chemical Engineering, or related field. * 1-3 years of experience in manufacturing, chemical formulation, or synthesis. * Ability to make improvements and recommendations to SOPs * Strong understanding of chemical interactions, solubility, and stability. * Excellent documentation and problem-solving skills. * Ability to work independently and in cross-functional teams. Work Environment The work environment includes operating various lab equipment and handling hazardous materials. The role requires maintaining a clean and safe lab setting and adhering to safety, quality, and regulatory standards. Job Type & Location This is a Contract to Hire position based out of Fremont, CA. Pay and Benefits The pay range for this position is $25.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fremont,CA. Application Deadline This position is anticipated to close on Jan 22, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Be part of our journey As a global leader in specialty chemicals, we continue to succeed and strengthen our delivery of innovative, sustainable, and high-performance solutions. We are passionate and excited about how we can develop and utilize new technologies to shape and inspire changes within an ever-growing marketplace. Incotec is the seed enhancement company, independently providing solutions through innovative technologies and services, focusing on customer needs. Position Summary: Incotec (Salinas, CA) is looking to add a Certified Seed Analyst or Registered Seed Technician to our team! The primary purpose of this role is to direct and manage all lab operations with overall responsibility for seed analysis (purity and germination) in accordance with Incotec and A.O.S.A standards. Other duties include but not limited to assisting with receipt and login of samples, initiating tests by preparing planting media, imbibing or planting seeds, or otherwise working with seeds, writing and establishing specifications, assisting in the validation of QC tests, and the writing of Standard Operating Procedures. How you will contribute (Duties & Responsibilities): * Responsible for maintaining quality standards in the department. * Adhere to all safety rules and programs. * Performs advanced tests for purity and germination potential on prepared seed samples to determine seed viability. * Conduct seed testing in accordance with AOSA, ISTA, CFIA, customer specifications, plans, work instructions, and any other regulatory protocol governing testing. * Determines seed sample germination potential through the use of proper substrate, temperature, moisture and the subsequent evaluation of seedlings. * Conduct and record results of physical purity on all species. Must be familiar with AOSA Rules, ISTA, Canada M & P, Federal Seed Act and other State Laws regarding noxious weeds. * Determines seed sample purity based on pure seed, other crop, inert matter, weed seed, noxious weed seed and prohibited weed seed content. * Oversee testing team personnel in the performance of daily testing activities, including preparation of testing resources that maximize efficiency, assist in testing activities, evaluation of data, interpretations of testing rules, and consultation of testing results. * Hire, train, develop and coach employees in germination testing activities. * Supervise and train Lab Technician(s) in proper A.O.S.A. procedures and techniques for preparing and testing seed samples. * Manage and maintain seed sample retention * Interpret and document test results. Oversees entry of test data results. * Operation and maintenance of laboratory equipment. * Back-up Quality Management in administrative duties as needed. Desired Skills and Experience (Qualifications): * Knowledge of seed quality, seed testing, and seed conditioning. * Knowledge of seed testing methods, chemicals, products, and equipment. * Knowledge of Quality Management System. * Excellent communication and written skills. * Proven supervisory experience. * Ability to apply conflict resolution skills. * Ability to work independently and as part of a team. * Ability to stand or sit for extended periods of time. * Ability to lift and carry samples, supplies and equipment as necessary. * Flexibility to work under seasonal time constraints. Education and Certifications: * Registered Seed Technologist/Certified Seed Analyst. * Advanced education or experience in an appropriate field of study. Application Information: Perks and Benefits: * Health & Wellness important to you? We've got you covered with benefits day 1! No waiting time for medical, dental & vision * Need a break? We've got your back with generous time off, including paid holidays, and extra days for the unexpected * Get paid and get moving with our Wellness Incentive Program! Annual employee reimbursement (up to $300) * Balance equals a healthy and happy community! We offer flexible work schedule, telecommuting * Planning for the future? 401(k) with company-match, ESPP, tuition reimbursement and online/onsite courses Hourly Base Pay Range: $23.00 to $29.00 This range reflects the base pay the company reasonably expects to pay for this position. Actual compensation will be determined based on factors such as geographic location, experience, education, and skill level. Additional compensation, such as annual bonuses or other incentives, may be offered based on eligibility and company policies. Croda recognizes employees as our strength and the diversity they bring to our workforce is directly linked to our ongoing success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including age, race, color, religion, national origin, gender, sexual orientation, gender identity, gender expression, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. In accordance with applicable law, we make reasonable accommodations for applicants' and employees' religious practices and beliefs, as well as any mental health or physical disability needs. Equal Opportunity Employer/Disability/Veterans. This Organization Participates in E-Verify.

Shift: Monday -Friday 2: 00 PM -10: 30 PM with overtime and weekend hours as needed Duration: 12 Months Pay range: $25.30 Hourly - $25.30 Hourly Onsite Job 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 specialized 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: No previous work experience required •Preferred: Previous work experience in manufacturing, operations, production or 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 •Ability to 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. 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 Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Duties and Responsibilities: * Perform inspections of purchased parts according to acceptance criteria using standard sampling plan. * Able to perform First Article Inspection (FAI) of manufactured parts, electromechanical assemblies and final assemblies. * Physical, mechanical and/or electrical measurements in compliance with the company Quality System. * Accurately document results of inspection / testing and maintain controlled document files, logs and test records. * Inspect cables per wiring configuration. * Initiate non-conformance process and assist in resolving non-conformances. * Monitor receiving inspection backlog. * Able to be flexible with the work schedule. * Process SAP transactions to segregate and disposition non-conforming product. * Other duties and responsibilities in the Quality Department as assigned. * Ability to conduct basic troubleshooting and problem resolution. Education and Experience: * High School Diploma or Equivalent. Preferred one year of experience in an FDA regulated environment and/or ISO 13485 standards in the medical device industry and/or in-vitro diagnostics preferred. Technical and physical position requirements: * Familiar with measuring equipment such as micrometer, caliper height gauges, plug gauges. * Able to lift at least 35 lbs. * Strong attention to details and ability to understand and follow complex procedures. * Working knowledge and experience in basic computer applications such as Microsoft Word, Excel and Outlook. * Effective and clear written and verbal communication skills in English language. The US base salary range for this full-time position is $20.60 - $31.60. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the base pay target range for new hire salaries for the position. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. In addition to compensation, Zoetis offers a comprehensive benefits package that supports the physical, emotional and financial wellbeing of our colleagues and their families including healthcare and insurance benefits beginning on day one, a 401K plan with a match and profit-sharing contribution from Zoetis, and 4 weeks of vacation. Visit zoetisbenefits.com to learn more. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

QC Technician (Salinas/Yuma) Duda Farm Fresh Foods, Inc. is seeking a Quality Control (QC) Technician for an immediate opening. This role is responsible for ensuring that all incoming products meet USDA standards, DFFF requirements, and customer specifications. The position reports directly to the National QC Manager and will be based in Salinas, CA and Yuma, AZ. Essential Job Responsibilities Inspect all loads arriving at the facility-whether from the field or purchased-to ensure finished, packed commodities meet USDA, DFFF, and/or customer-specific specifications. Periodic field-level inspections may be required. Report any issues in real time to the appropriate management. Verify PTI labels and pallet license plates for product description, legibility, and accurate best-by/use-by dates. Perform daily temperature checks on on-hand commodity inventory to ensure proper temperature maintenance. Complete bi-weekly age reports (Monday and Thursday) on inventory to confirm quality and food safety standards. Immediately report any deviations, such as rapid quality loss or compromised product. Submit inspection documents to the Manager for daily verification. Address all deviations in real time and ensure proper documentation and organized storage. Confirm that measuring devices (e.g., thermometers) are calibrated daily and maintain calibration records. Conduct food safety visual inspections during quality checks. Report any foreign material or concerns to Management immediately for corrective action. Ability to travel between growing regions to cooling facilities in Salinas, CA (April to November) & Yuma, AZ (November to March). Follow all safety work practices by following safety rules and regulations. Comply with all company policies and procedures. Must use all required PPE (Personal Protective Equipment). Must be able to work without directions and stay productive. Must be dependable, punctual, and able to work flexible hours as needed. Must be able to work weekends. Must be able to work overtime when requested. Other duties as assigned. Required Knowledge Skills and Abilities: High School diploma required Bilingual preferred but not required. Agriculture or demonstrated interest in agriculture preferred Valid CA driver's license Basic knowledge of Microsoft Word, Outlook and Excel preferred. Working Conditions: Working environment will include warehouse, cold room and/or field. Works well on own and in a team environment. Must be willing to work outside of normal business hours (8:00AM-5:00PM) and weekends when necessary. Ability to perform physical labor, including lifting up to 65 lbs. and working in outdoor environments. Regular climbing, stooping and bending required. Overnight travel may be required. Benefits: 401(k) 401(k) matching Dental insurance Disability insurance Employee assistance program Flexible spending account Health insurance Life insurance Paid sick time. Paid time off Vision insurance Job Type: Full-time Pay: $25.00 Duda Farm Fresh Foods provides a fair and equal employment opportunity for all employees and job applicants regardless of race, color, religion, national origin, gender, sexual orientation, age, marital status or disability. We expect and require the cooperation of all employees in maintaining a discrimination and harassment-free work environment. We offer an excellent benefit package as part of our total compensation including medical, dental and vision insurance, 401K, flexible spending accounts, tuition reimbursement program, paid time off and much more. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Due to the high volume of applications received, only those candidates who are selected for interviews will be contacted.

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. Duties & 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 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 * Organizing * Judgement * 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 mange time and prioritize multiple task in a fast paced environment * Proficient in use of MS Office applications, MS Project, Outlook * May require international travel and international business experience * Knowledge of Lean manufacturing fundamentals

Shift: 1st shift, Monday-Friday, Standard working hours Duration: 12 Months Pay range: $25.00 Hourly - $25.00 Hourly Onsite Job The Formulations Lab Wash Technician supports the manufacturing process by cleaning, sanitizing, and preparing lab equipment and materials used in buffer and reagent production. This role ensures all cleaning procedures meet cGMP and safety standards, playing a critical role in maintaining a clean and compliant lab environment. Key Responsibilities: •Clean and sanitize stainless steel tanks, glassware, utensils, and other lab equipment according to SOPs and cGMP requirements •Operate and maintain washers, autoclaves, and other sterilization equipment •Prepare tanks and materials for sterilization, including wrapping and loading/unloading from the autoclave •Assist in routine preventive maintenance and minor troubleshooting of washroom equipment •Transport clean equipment and materials to appropriate staging areas for use in production •Maintain accurate cleaning logs and documentation •Follow safety procedures when working with cleaning agents and potentially biohazardous materials •Notify supervisor of any damaged equipment, procedural deviations, or safety concerns •Maintain stock of cleaning supplies and request resupply as needed •Perform other duties as assigned Minimum Requirements / Qualifications: •High school diploma or equivalent required •Previous experience in a laboratory, pharmaceutical, or manufacturing environment preferred •Ability to follow written and verbal instructions precisely •Strong attention to detail and good documentation practices •Ability to lift up to 50 lbs and work on feet for extended periods •Comfortable working in a cleanroom or controlled lab environment Non-Negotiable Hiring Criteria: •Must comply with GMP, QSRs, ISO, and IVD regulations at all times •Ability to read, write, and understand English instructions •Basic math skills for measurements and inventory counts •Willingness to work in an environment with chemical and biological materials •Basic computer skills;familiarity with Microsoft Outlook and Excel preferred Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

1X Since its founding in 2015, 1X has been at the forefront of developing advanced humanoid robots designed for household use. Our mission is to create an abundant supply of labor through safe, intelligent humanoids. We strive for excellence in all we do, solving some of the hardest problems in robotics with the world's most talented individuals. Every part of our robots is designed and produced in house, from motor coils to AI, reflecting our vertically integrated approach. At 1X, you will own real projects, be recognized for your achievements, and be rewarded based on merit. We are seeking a Lab Chemistry Technician who is passionate about hands-on experimentation and eager to support the creation of advanced materials for next generation humanoid robots. This role is ideal for someone who enjoys preparing materials with precision, running characterization tests, executing polymer and other organic synthesis reactions, and working closely with senior scientists in a fast paced laboratory environment. You will work directly under the supervision of the Polymer Chemist and the Materials Science Lead, supporting the development of elastomers, coatings, adhesives, textiles and multilayer material systems that enable future robot architectures. Key Responsibilities * Prepare polymer formulations, elastomers, textiles and composite samples, and perform hands-on laboratory experiments including the synthesis and modification of polymers under senior scientist supervision. * Operate laboratory equipment for mixing, curing, casting, coating, laminating, and other processing of soft material systems. * Execute and improve synthesis workflows using glass and stainless reactors, feed pumps, temperature controllers, nitrogen purging systems, and filtration equipment, following SOPs for start up, shut down, and cleaning. * Conduct material characterization such as tensile testing, hardness measurements, rheology, thermal analysis, adhesion testing, and visual inspection. * Maintain meticulous laboratory records, document procedures and results, and contribute to technical reports when required. * Communicate results, observations, and interpretations clearly and proactively to supervising scientists. * Maintain an up to date SDS database and ensure proper labeling, handling, storage, and inventory management of chemicals and materials. * Perform all work in a safe and responsible manner, follow established safety procedures, and contribute to ongoing improvements in lab safety practices and workflows. * Uphold strict confidentiality and maintain awareness of intellectual property responsibilities. * Assist in building small scale prototypes, participate in pilot processing trials, and support rapid iteration across multiple experiments. * Help maintain an organized laboratory environment that supports efficient workflow, safety compliance, and reliable daily operations. * Work effectively within a diverse team, demonstrating initiative, accountability, and steady progress toward objectives and milestones.