Quality control analyst jobs in Mountain View, CA - 197 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

A cutting-edge AI startup is seeking an experienced AI Researcher to drive innovative research in generative AI and build multimodal foundation models. Ideally located in San Francisco, the candidate will require a PhD and 5+ years in the field. Responsibilities include designing and implementing models, conducting independent research, and publishing findings. This role is central to advancing AI for earth observation and creating a positive impact. #J-18808-Ljbffr

Join Camb.ai's Speech R&D team to lead innovative speech tech research, integrate findings, and set benchmarks in AI-driven dubbing and Join Camb.ai's pioneering AI team. Lead Speech R&D, integrate tech into products, publish research, and innovate in speech recognition and synthesis. About The Internet was made for English speakers. We are redesigning it for the world. At Camb.ai, we're pioneering the future of AI-driven dubbing, localization, speech synthesis and NMT. Powered by our state-of-the-art models in zero-shot performance transfer and colloquial translation, we're not just innovating; we're setting SOTA benchmarks. Backed by elite global VCs, partnering with enterprise giants and top influencers, guided by an AI leadership with five $100Mn ARR successes, we're seeking top‑tier talent to expand our AI research team comprising of individuals from Carnegie Mellon, Apple and more. Responsibilities Lead and drive innovative research in the field of speech recognition, synthesis, and related technologies. Collaborate closely with the R&D team to integrate research findings into Camb.ai's products. Keep abreast of latest advancements in speech technology and continuously push for innovations in the field. Publish research findings in leading conferences, journals, and workshops. Qualifications PhD or equivalent experience in speech technology, machine learning, or a related field. Proven track record of publishing in leading speech conferences such as Interspeech, ICASSP, etc. Hands‑on experience with popular speech toolkits and frameworks. Strong programming and algorithmic skills. To Apply Please send your resume to *************** with the subject line "Speech R&D Researcher - [Your Name]" in the subject line. Featured Thinking from CAMB.AI Handpicked stories on AI, localization, and reaching audiences worldwide. #J-18808-Ljbffr

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

The Senior Lead Analyst in Analytical Quality Control serves as a technical expert in complex analytical testing and instrumentation, providing leadership, mentorship, and project management for quality control activities within a cGMP environment. This role is a high-level individual contributor position that bridges technical expertise with leadership responsibilities, ensuring product quality, compliance, and data integrity within a biopharma manufacturing organization. Reporting to: Associate Director, Quality Control Analytical Location: Newark, CA Salary Range: $115k - $130k + Bonus * The final salary offered will depend upon factors that may include but are not limited to the quality and length of experience, education, and geographic location. Responsibilities/Essential Duties: Analytical Testing: Performing and reviewing complex analytical tests for raw materials, in-process samples, and finished products using techniques such as HPLC, UPLC, LCMS, ELISA, CE-SDS, and various compendial methods. Documentation and Compliance: Authoring, reviewing, and approving GMP documentation, including SOPs, test methods, protocols, technical reports, and quality records (deviations, OOS, CAPAs, Change Controls). Ensuring all activities adhere to cGMP and GLP. ICH, FDA, and EMA guidelines. Troubleshooting and investigation: Acting as a subject matter expert (SME) to troubleshoot complex equipment and method issues, and leading thorough investigations into out-of-specification (OOS) or out-of-trend (OOT) results using root cause analysis tools. Method Lifecycle Management: Leading and supporting the development, optimization, transfer, qualification, and validation of analytical methods for new and existing products. Leadership and Training: Mentoring and training junior analysts, guiding staff in laboratory procedures, and potentially managing day-to-day team activities and resource allocation. Project and Cross-Functional Collaboration: Leading projects and collaborating with cross-functional teams such as Manufacturing, Quality Assurance, Regulatory, and Analytical Development to meet deliverables and support regulatory inspections. Basic Qualifications: Bachelor of Science in Biochemistry, or a related pharmaceutical biotechnology discipline 8+ years in a Quality Control laboratory, specifically within a cGMP biopharmaceutical or pharmaceutical environment for a commercially approved product. Must have extensive hands-on experience with relevant analytical instrumentation and software (e.g., Empower, SoftMax, LIMS) Must be detail-oriented and have experience in formal technical writing for Quality Control laboratories (e.g., SOPs, Quality Records, Method Validation/Transfer Protocols, Method Validation/Transfer Reports). Must have extensive experience in peer-reviewing of Quality Control data. Experience with the management of stability studies, stability data analysis, and stability data report generation. Experience in scheduling of Quality Control analytical testing for a team of analysts with throughput time adherence. Experience with CMO support for external operational management. Must have experience in Lean Six Sigma methodologies for bottleneck reductions and high throughput efficiencies in a commercial manufacturing environment. Preferred Qualifications: Master of Science in Biochemistry, or a related pharmaceutical biotechnology discipline Effective written and verbal communication skills Lean Six Sigma Black Belt or PMP experience using Lean methodologies for process improvement. Critical reagent management experience (procurement, preparation, qualification, and management of inventory) is preferred. Raw Material management experience in sampling, qualification, and management of testing activities. Company Summary: Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. With a differentiated portfolio of products spanning 60 countries, Revance meets the evolving needs of patients and consumers worldwide through continued innovation and commercialization of new products and treatments. What Revance invests in you: Competitive Compensation, including base salary and annual performance bonus. Flexible PTO, holidays, and parental leave. Generous healthcare benefits, HSA match, 401k match, employer-paid life and disability insurance, pet insurance, wellness discounts and much more! This section of the is required by the Americans with Disabilities Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship. A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.” Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Job Description 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.

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.

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

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

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 Feb 11, 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.

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.

Scope/Responsibilities of Role: Helping design AI systems that write regulatory documents. Deconstructing authoring/review/QC heuristics for engineers. Evaluating AI-generated content quality and identifying edge cases. Bridging the gap between domain expertise (medical writing) and technical product development. Must Have Skills for Role: 3+ years of medical writing experience in regulatory affairs. Direct experience with CTD documents (non-clinical and CMC). Knowledge of FDA, EMA, and ICH guidelines. Ability to extract and document rules/logic for technical teams. Strong QC capabilities. Nice to Have Skills for Role: Familiarity with structured content formats like XML or JSON. Experience working with life sciences software tools.

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.

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.

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.

Shift: Monday -Friday with overtime and weekend hours as needed Duration: 12 Months Pay range: $23.00 Hourly - $23.00Hourly 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.