Quality control analyst jobs in Tracy, CA - 171 jobs

A construction safety company based in California is seeking a Traffic Control Associate responsible for managing traffic around work zones. Applicants must possess a valid California Driver's License and demonstrate strong interpersonal skills. The position involves coordinating traffic flow, setting up safety equipment, and ensuring the safety of all personnel involved. Potential candidates should have a high school diploma and experience in a similar role is preferred. We offer competitive wages and a robust benefits package. #J-18808-Ljbffr

The Opportunity: The Palate of a Chef, the Mind of a Scientist TCHO is looking for a rare professional to serve as the tactical engine of our research and production. This individual will fill a high-impact role that bridges the gap between creative sensory exploration and technical production. This is a hands-on role at our factory, responsible for tending the entire lifecycle of our chocolate. This begins with the cacao beans being grown around the world by our farmer partners, to the final production of high-end chocolate and confections at our production facility in Berkeley. We are seeking a maker who can manage complex data and production schedules while maintaining a disciplined focus on creativity and flavor. This position is 100% onsite due to the hands-on nature of the role, including production, sensory evaluation, laboratory work, and small-batch confectionery manufacturing. 1. Sensory Mastery & Tasting Daily Analysis: Lead disciplined daily sensory panels of raw cacao liquors, experimental batches, finished chocolate, and confections to ensure every product meets TCHO standards. Raw Material Selection: Participate in the selection and sensory analysis of all raw materials, including cocoa beans, liquor, powder, butter, and inclusions such as nuts or vanilla. Final Sign-off: Provide sensory sign-off for final products coming off the line to ensure manufacturing quality and consistency. 2. The “Source” & Laboratory Management Bean Sample Management: Manage the intake of cacao samples from global partners, including roasting, winnowing, and grinding micro-batches to evaluate fermentation quality and genetic potential. Flavor Lab Oversight: Manage daily operations of the flagship TCHO Flavor Lab space (one of only 12 worldwide). Operational Upkeep: Oversee lab organization, cleaning, sample retention, and restocking of laboratory supplies and equipment. 3. Production, Formulation & Retail Confectionery Formula Creation: Develop and manage proprietary daily production formulas used by the manufacturing team. Retail Confectionery Production: Act as a Confectioner for TCHO Retail, responsible for creating small-batch and small-lot confections for retail customers, including hand-crafted and limited-run items. Efficiency & Scalability: Support factory operations by optimizing run times, flush materials, FIFO practices, and small-batch scalability. SOP Compliance: Ensure all product SOPs are followed, including requirements related to cross-contamination, Organic, Kosher, and Fair Trade certifications. 4. New Product Development (NPD) Dream-to-Reality: Translate creative product concepts into consistent, repeatable production. Prototyping: Execute hands-on prototyping and produce sales and retail samples, including chocolate formulas, plant-based ganache, enrobed items, panned goods, and other confections. Scaling: Move products from lab-scale concepts to small industrial and retail-ready production. Who You Are Palate-Driven: You possess an advanced ability to articulate flavor and a deep interest learning how the magic of chocolate comes to life. Analytical: You love a good system and can track R&D data and formulas with precision to keep projects on a professional timeline. Technically Grounded: You likely have a background in Food Science, Pastry, or Confectionery and know your way around the bakery and confectionery world. Onsite & Flexible: This is not a desk job. You are based at our Berkeley HQ and willing to work weekends to keep the lab and production cycles moving. Skills & Abilities Bachelors' degree or equivalent Minimum 3 years working in pastry, confectionary or chocolate industry, Demonstrated leadership experience of teaching and developing teams within food industry. Excellent writing, reading and communication skills Spanish fluency is a major plus. Ability to transport and move 50-pound handloads Must be able to remain in a stationary position for entire shift Must be able to work above ground levels-10 feet and in cold and warm temperature work environment Salary Range - $95,000 - $120,000

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.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Title: Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Job Description: Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to support analytical testing for a wide variety of methods to reach department timelines Position duties & responsibilities: The candidate will perform routine Clinical and Development testing activities with expertise in a wide variety of methods ranging from Chemistry to Biochemistry involving, but not limited to, HPLC, ELISA,qPCR, A280, Western Blot, PAGE, Protein Concentration, Osmolality, etc. Additionally, candidate will review data generated by other analysts on these, as well as other methods, with appropriate training. Must be able to follow Standard Operating Procedures (SOPs) in performance of laboratory testing to complete assigned tasks to meet release timelines and ensure quality. Must be able to document test results accurately and legibly to meet regulatory requirements and ensure completeness and accuracy per cGMPs and/or cGLPs. Must be able to compile and enter data into LIMS, Excel, or other application as needed, to be used for tracking and trending purposes. Experience using ChemStation, SoftMaxPro, and OpenLAB a plus. Qualifications Requirements/Preferences Education Requirement(s): BS/BA Ideal candidate will have 2+ years of experience in a cGMP laboratory environment with demonstrated ability to learn new skills to achieve proficiency. Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) 10 Exchange Place, Suite 1710, Jersey City, NJ 07302 Whats app: ************** Twitter: @mayankpharma Additional Information All your information will be kept confidential according to EEO guidelines.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Bachelor's degree in Biology/Microbiology/Medical Technology or similar field with 2 years' work experience; Or a Master's degree in the same field with no work experience. • This person should be detail-oriented and a team player. • Duties: Endotoxin assay, Mycoplasma qPCR assay, Total Organic Carbon assay, Rapid Microbial Detection assay, Cell banking, FACS analysis, aseptic distribution of liquid antibodies Qualifications Bachelor's degree in Biology/Microbiology/Medical Technology or similar field with 2 years' work experience; Or a Master's degree in the same field with no work experience. with QC experience Additional Information Thanks & Regards Riya Seth ************

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

Build Your Career. Build America's Future. Vulcan Materials Company is the nation's largest producer of construction aggregates and a major producer of aggregates-based construction materials including asphalt and ready-mixed concrete. When you join Vulcan, it's more than starting an exciting career - you get to make a difference for millions of people every day across the country. When you join Vulcan, you join a dynamic culture in which career development is encouraged, excellence is rewarded, and diversity is valued. No matter the role or the location across the country, every member of the Vulcan team lives through the Vulcan Way: doing the right thing, the right way, at the right time. We're Coming Back Together To Be Together 100% In Office & Onsite At Vulcan Materials, we believe that the heart of our success lies in the strength of our engagement, our connection, and our commitment to developing our people. We are excited to restore the collaborative in-person environment that fuels our innovation and growth. This move is not just about being physically present; it's about reigniting the spirit that comes from face-to-face interactions, fostering a collaborative, inclusive culture where every voice is heard and everyone thrives. What You'll Do: Ensure Quality Control. Conduct routine testing of in-process materials, raw materials, environmental samples, and finished materials to ensure quality control of products at the point of production, shipping, and arrival upon the job site. Adhere to testing methods, including American Society for Testing and Materials (ASTM), American Association of State Highway and Transportation Officials (AASHTO) and Department of Transportation (DOT). Document and Report Information. Complete all required reports in a timely and accurate manner, interpreting, documenting, and storing the results. Communicate test results in a timely manner to the supervisor and properly document in a database. Maintain Lab Standards. Ensure housekeeping standards are maintained in and around the lab. Troubleshoot problems and review basic product specifications. Inspect, calibrate, and maintain testing equipment periodically. Monitor Stockpile. Inspect stockpiles, materials sources, and truckloads at plant sites. Monitor the daily construction of the stockpile to ensure that segregation and contamination is kept to a minimum or eliminated. Notify management immediately if contamination is identified. Inspect Equipment and Structures. Conduct routine inspections of the plant equipment in order to ensure safe, reliable, and compliant operations to maximize production and minimize interruptions. Additional Responsibilities. Other duties as assigned. Skills You'll Need: Experience. Prior training or experience in the materials testing field is preferred. Knowledge of general principles and practices of aggregate production is preferred. Safety Knowledge. Must display knowledge and awareness of construction and mining site hazards. Math Skills. Must possess good math skills and demonstrate the ability to perform simple to moderately complex arithmetic calculations. Technology Skills. Must have the ability to use computerized equipment and technology. Must be proficient in Microsoft Office Suite, Google, Oracle Business Environment, and other software packages relevant to the position. What You'll Like About Us: Great Company Culture. Our people share a competitive drive for excellence in an environment of trust, teamwork, open-mindedness and communication. Safe. Industry leader in health and safety standards. We are committed to creating a safe work environment and protecting all employees and customers. Meaningful Work. What sets up apart is the work we do impacts daily lives - and every employee contributes. Our aggregates produced are used to build roads, schools, hospitals, airports, and housing throughout the United States. Health Benefits. Medical, Dental, Vision programs, plus much more. Rest and Relaxation. Paid vacation, personal floating days, and paid holidays. Prepare for the Future. 401(k) with company match and contribution. Training and Development. We see our development programs and helping our employees meet their goals as a key part of our business. Salary Range: the base salary range for this role is between $30.00 to $36.00 per hour. This range is not inclusive of our discretionary bonus or equity package. When determining a candidate's compensation, we consider a number of factors, including skillset, experience, job scope, and current market data. Vulcan Materials Company is committed to employing a diverse workforce. You will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, or disability. You also have the right to be free from discrimination for medical needs arising from pregnancy, childbirth, or related medical conditions. NOTICE TO TEMPORARY STAFFING AGENCIES, PLACEMENT SERVICES AND PROFESSIONAL RECRUITERS Vulcan Materials Company has an internal recruiting department. Please review our policy as it relates to the use of temporary staffing agencies, placement services and professional recruiters.

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

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.

About AllAccem AllAccem, Inc., founded in 2005, is a medical device and pharmaceutical company focused exclusively on developing and manufacturing products for veterinary healthcare. We manufacture, market, and sell professional veterinary products globally. AllAccem operates as a standalone entity within the Vimian Group. While part of the broader Vimian family-alongside companies such as Movora-AllAccem functions independently with its own products, manufacturing operations, and organizational culture. This role is fully embedded within the AllAccem team and supports on-site manufacturing operations in San Carlos, CA. Position Summary The Associate Chemist is a hands-on role supporting routine chemical manufacturing operations under established standard operating procedures (SOPs). This position is well suited for individuals early in their professional careers or those transitioning into an industrial manufacturing environment who are seeking to build practical experience in regulated production settings. The Associate Chemist works under the guidance of senior chemists and contributes to the reliable execution of production activities, documentation, and equipment preparation. Salary $75-95K DOE Key Responsibilities Manufacturing & Production Support * Execute assigned chemical synthesis, purification, and isolation steps in accordance with approved SOPs and batch records. * Support multi-kilogram scale production activities through accurate execution of defined procedures. * Assist with preparation of reagents, starting materials, and production areas for scheduled manufacturing runs. Documentation, Quality & Compliance * Accurately record production data and observations in batch records and associated logs. * Follow all quality system requirements, safety procedures, and cleanroom or controlled area practices. * Escalate deviations, equipment issues, or safety concerns to senior staff or supervision. Equipment, Housekeeping & Safety * Clean, maintain, and stage glassware, tools, and production equipment for daily operations. * Assist with setup and teardown of manufacturing equipment, including inert-atmosphere systems. * Maintain a clean, organized, and inspection-ready work environment. Requirements * BA or BS in Chemistry or a closely related scientific discipline. * Academic or internship experience with organic synthesis and basic purification techniques. * Familiarity with laboratory safety practices and chemical handling. * Ability to lift up to 30 lbs and stand for extended periods. Preferred Qualifications * Exposure to industrial, manufacturing, or regulated laboratory environments (internships, co-ops, or entry-level roles). * Introductory experience with SOPs, batch records, or quality-controlled documentation. * Basic familiarity with inert-atmosphere techniques (e.g., glovebox or Schlenk line) through coursework or research. Knowledge, Skills & Abilities * Strong attention to detail and willingness to follow written procedures precisely. * Good manual dexterity and hand-eye coordination. * Ability to learn new processes quickly in a production-focused environment. * Clear communication skills and ability to work effectively as part of a team. Equal Opportunity Employer Statement AllAccem, Inc. is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees. All employment is decided on the basis of qualifications, merit, and business need. We do not discriminate based on race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), sexual orientation, gender, gender identity, gender expression, national origin, ancestry, age (40 and over), disability (mental and physical), genetic information, marital status, military or veteran status, or any other basis protected by federal, state, or local law. Pursuant to the California Equal Pay Act, AllAccem, Inc. does not ask about or consider current or past compensation when determining an applicant's salary. Pay will be based on the job-related skills, experience, and education of the selected candidate. We are also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. We actively encourage candidates from all backgrounds to apply for our positions. We believe that a diverse workforce enhances the quality and innovation of our work. Join us in fostering an environment that promotes equal opportunities and celebrates diversity. If you need assistance and/or a reasonable accommodation in the application or recruiting process, please contact ************* Salary Description $75-95k

About AllAccem AllAccem, Inc., founded in 2005, is a medical device and pharmaceutical company focused exclusively on developing and manufacturing products for veterinary healthcare. We manufacture, market, and sell professional veterinary products globally. AllAccem operates as a standalone entity within the Vimian Group. While part of the broader Vimian family-alongside companies such as Movora-AllAccem functions independently with its own products, manufacturing operations, and organizational culture. This role is fully embedded within the AllAccem team and supports on-site manufacturing operations in San Carlos, CA. Position Summary The Associate Chemist is a hands-on role supporting routine chemical manufacturing operations under established standard operating procedures (SOPs). This position is well suited for individuals early in their professional careers or those transitioning into an industrial manufacturing environment who are seeking to build practical experience in regulated production settings. The Associate Chemist works under the guidance of senior chemists and contributes to the reliable execution of production activities, documentation, and equipment preparation. Salary $75-95K DOE Key Responsibilities Manufacturing & Production Support Execute assigned chemical synthesis, purification, and isolation steps in accordance with approved SOPs and batch records. Support multi-kilogram scale production activities through accurate execution of defined procedures. Assist with preparation of reagents, starting materials, and production areas for scheduled manufacturing runs. Documentation, Quality & Compliance Accurately record production data and observations in batch records and associated logs. Follow all quality system requirements, safety procedures, and cleanroom or controlled area practices. Escalate deviations, equipment issues, or safety concerns to senior staff or supervision. Equipment, Housekeeping & Safety Clean, maintain, and stage glassware, tools, and production equipment for daily operations. Assist with setup and teardown of manufacturing equipment, including inert-atmosphere systems. Maintain a clean, organized, and inspection-ready work environment. Requirements BA or BS in Chemistry or a closely related scientific discipline. Academic or internship experience with organic synthesis and basic purification techniques. Familiarity with laboratory safety practices and chemical handling. Ability to lift up to 30 lbs and stand for extended periods. Preferred Qualifications Exposure to industrial, manufacturing, or regulated laboratory environments (internships, co-ops, or entry-level roles). Introductory experience with SOPs, batch records, or quality-controlled documentation. Basic familiarity with inert-atmosphere techniques (e.g., glovebox or Schlenk line) through coursework or research. Knowledge, Skills & Abilities Strong attention to detail and willingness to follow written procedures precisely. Good manual dexterity and hand-eye coordination. Ability to learn new processes quickly in a production-focused environment. Clear communication skills and ability to work effectively as part of a team. Equal Opportunity Employer Statement AllAccem, Inc. is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees. All employment is decided on the basis of qualifications, merit, and business need. We do not discriminate based on race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), sexual orientation, gender, gender identity, gender expression, national origin, ancestry, age (40 and over), disability (mental and physical), genetic information, marital status, military or veteran status, or any other basis protected by federal, state, or local law. Pursuant to the California Equal Pay Act, AllAccem, Inc. does not ask about or consider current or past compensation when determining an applicant's salary. Pay will be based on the job-related skills, experience, and education of the selected candidate. We are also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. We actively encourage candidates from all backgrounds to apply for our positions. We believe that a diverse workforce enhances the quality and innovation of our work. Join us in fostering an environment that promotes equal opportunities and celebrates diversity. If you need assistance and/or a reasonable accommodation in the application or recruiting process, please contact ************* Salary Description $75-95k

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

Join our innovative team at Batchline Solutions where we are committed to help more food brands redefine the dining experience for their customers by blending creativity, practicality, and smart solutions. Our team of culinary experts includes award-winning chefs, presidents of iconic food brands, and over 70 years of combined business, operations, and technology experience-not to mention, an unwavering passion for food. We are currently seeking highly motivated individuals to fill the Quality Control Associate Level 1 role at our food manufacturing facility 18675 Madrone Pkwy, Morgan Hill CA, 95037. The primary responsibilities of this role is to monitor and inspects established food safety and quality assurance functions in support of our commitment to our customers and our Mission Statement. This position is expected to interact across inter-departmental boundaries in a professional manner that exemplifies a collaborative spirit. All Intelligent Foods employees are also required to adhere to Good Manufacturing Practices (GMPs), food handling procedures, quality control, and all safety procedures and policies in our distribution centers. What will you be doing: Ability to consistently execute tasks according to SOP (Standard Operating Procedures) SSOP (Sanitation Standard Operating Procedure) and GMP (Good Manufacturing Practices) for the production center as trained. Ability to perform basic food safety practices in the production center with a high degree of attention to detail and internal customer service. Ability to provide support in all areas related to the lab and testing of products. Ability to demonstrate accurate and safe use of basic warehouse equipment including but not limited to pH meter and luminometer. Responsible for inspections, process audits, product testing, analyzing measurements and overseeing production processes to ensure high quality products. Responsible for maintaining quality control standards by properly investigating, correcting and communicating any in process or finished product quality issues immediately. Responsible for completing and reviewing in process and finished product documentation to ensure accuracy. Qualifications Who you are and why you're right for us: At least 6 months experience in warehouse setting is preferred. High school diploma or equivalent preferred Ability to read and follow written and/or verbal instructions in English. Attention to detail, accuracy, thoroughness, and flexibility required Basic computer skills required (Microsoft Word, Internet search, Data Entry, Email) Ability to work in a fast-paced environment, a variety of shifts, weekends, and overtime as needed. Ability to work independently and or in a group setting, with minimal supervision. Ability to work in a refrigerated environment (-9º-42º Fahrenheit) for 8 or more hours and in some instances, in a dark environment Why Join Us: Medical, Dental, Vision and Life Insurance HSA and FSA account options Employee assistance program Employee discount 401(K) with a match Paid Holiday and additional 2 Floating Holidays Paid time off (PTO) Access to our weekly internal Farmer's Market, where you can take home free quality produce and pantry items.

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

We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories , working together to enable a better, safer and more interconnected world. Our Hayward, CA laboratory is looking for an experienced laboratory analyst to join their team! The Lab Analyst will prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. The Lab Analyst works independently and as part of a team to meet daily production targets and ensure turnaround times are met. The Lab Analyst understands and applies basic science principles. The Lab Analyst always follows safe laboratory practices and maintains a safe working environment. Job Functions After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies Performs routine operation, maintenance, calibration of laboratory instruments/equipment Preparation and analysis of bulk and solid materials for asbestos content using PLM (Polarized Light Microscopy). Determination of visual percentage and optical properties of asbestos and non-asbestos material. Preparation and analysis of air, wipe, and bulk samples for metals analaysis. Entering sample data, analysis data and preparing reports on LIMS system Inputs and maintains technical information as needed to support the laboratory functions/operations. Adheres to internal standards, policies and procedures. Performs other duties as assigned. Work Schedule Monday - Friday 8 - 5 Occasional Overtime Qualifications Associate Degree in a Chemistry or similar scientific discipline and 3-5 years of years' relevant experience in Analytical Chemistry Laboratories (Required) Bachelor's Degree in a Chemistry or similar scientific discipline and 5+ years of years' relevant experience in Analytical Chemistry Laboratories (Preferred) Advanced English language skills (Required) Strong mathematical and reasoning skills (Required) Proficiency in Microsoft Office programs (Required) Ability to lift, carry, push, and/or pull upwards of 25 lbs on a frequent basis (Required) This position pays $26 - $28 per hour (dependent on experience) and is eligible for overtime pay. In addition, your compensation package includes the following benefits: Participation in the Company's benefit programs coincident or following the first of the month in which you are hired. Immediate eligibility to participate in the Company's 401K Retirement Plan Paid vacation Four (4) floating holidays annually Seven (7) company observed holidays paid Sick time accrual Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

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 RegularColleague 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.

Sirius Staffing is seeking Megasys Gas & Chemical Technicians in Fremont, CA. In this role, you will lead and support the technical demands of site gas and chemical equipment, ensuring compliance with operational and maintenance procedures, emergency preparedness, and flawless execution. If you're looking for a long-term career path with the opportunity to become a permanent employee (typically within 12 months), apply today! Shifts: Training Mon-Fri 7-4, approx. (3-5 weeks), Then, after training, you would transition into your assigned shift, a compressed shift, which includes working on the day shift for 3 months and then on night shifts for 3 months; it continuously rotates from days to nights. Compressed schedules: 12-hour schedules 6P - 6A, Sun, Mon, Tue, every other Wed 6P - 6A, Thur, Fri, Sat, every other Wed Pay Range: $27-30/hr.More experienced candidates: $30-$32/hr. Responsibilities: Support the onsite Project and Equipment team in gas and chemical operations, managing technical challenges for over 2,000 distribution equipment pieces across various types and vendors. Ensure compliance in writing, editing, and executing operating and maintenance procedures, promoting a ZERO safety or quality incident culture. Engage in projects, sustaining operations, safety processes, quality management, preventive maintenance, and training. Handle installations, decommissioning, troubleshooting, and repairs of all gas systems. Perform cylinder and drum changes on chemical and gas systems and resolve complex equipment issues. Demonstrate comprehensive knowledge of gas or chemical applications in wafer fabrication. Qualifications: Must have: 2 - 3 years of experience with chemicals and/or gas High School diploma or equivalent required Must have a valid Driver's license Clear English communication skills Clean-shaven to wear a respirator (when needed) Preferred Qualifications: 5+ years of experience with gas and chemical systems in a semiconductor ultra-high purity operation as an equipment technician. Associate degree or equivalent experience in electronics, design, or engineering. Navy Nuclear Power School trained Why Join Us? Weekly Pay Competitive Pay Comprehensive Benefits Package (available after the required waiting period) Medical Insurance - Provided through Cigna, covering routine wellness services at no cost, plus high and low plan options Prescription Coverage Options Vision & Dental Coverage through Guardian Supplemental Life Insurance with AD&D and Dependent Options Short-Term & Long-Term Disability Coverage Voluntary Accident, Critical Illness, and Cancer Insurance Cyber and Legal Coverage Options Telemedicine Options & Employee Assistance Program (EAP) Exciting Career Growth Opportunities Supportive and Inclusive Work Environment Sirius Staffing is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to characteristics such as race, color, national origin, religion, gender, age, marital status, disability, veteran status, citizenship status, sexual orientation, gender identity, or any other status protected by law.

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.