Quality control analyst jobs in Milpitas, CA

Join Ultimate Staffing to work onsite at our customer in San Jose CA. Are you passionate about clean energy and eager to help build the future of battery technology? We are pioneering the first anode-less solid-state battery cell, offering higher energy density, lower material costs, and streamlined manufacturing. We're looking for a R&D Technicians -Cell Build (Contractor) to join our All-Solid-State Battery team and support the development of next-generation battery cells. This is a 12-hr. shift -6:30 PM- 6:30 am Sat-Tue and 6:30 PM- 6:30 am Wed- Sat What You'll Do: Handle sensitive materials in gloveboxes, dry rooms, and fume hoods using proper PPE. Operate cell assembly tools, heated antechambers, presses, and metrology equipment. Follow SOPs for setup, cleanup, and troubleshooting. Collaborate with engineers and technicians to improve processes. Document experiments and prepare samples for testing. Shift: 12-hr. shift -6:30 PM- 6:30 am Sat-Tue and 6:30 PM- 6:30 am Wed- Sat What We're Looking For: High school diploma and 1+ year experience in R&D or manufacturing. Comfortable working in dry rooms/gloveboxes with fine motor skills and lifting up to 25 lbs. Willingness to wear a PAPR breathing apparatus. Detail-oriented, safety-conscious, and adaptable. Strong communication skills and proficiency in Outlook, SharePoint, and Microsoft Office. Preferred Qualifications: Experience with gloveboxes and dry rooms. Familiarity with metrology tools (e.g., imaging, radiography). Background in cell assembly. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

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

Working in a team of media process technicians, media process technician I will manufacture dehydrated and liquid cell culture media. Formulation technician will be able to follow batch record instructions and will be expected to weigh microgram to kilograms quantities of individual raw materials, calibrate equipment, follow safety policies and procedures, operate milling equipment, perform sterile filtration and any other tasks required to complete cell culture media manufacturing. Standard product testing, such as osmolality, pH and turbidity, will also be performed in this job. This position works closely with R&D, procurement, quality, process technology, marketing as well as external and internal customers and vendors RESPONSIBILITIES: Responsible for the staging and compounding of raw materials within weight tolerances (e.G. Micrograms to kilograms), milling, blending, aseptic liquid filling, process control monitoring and documentation of such procedures for manufacturing dehydrated culture media and liquid media in accordance with production schedules following the appropriate GMP and department procedures Completes all required documentation neatly, accurately, and in accordance with GMP. Performs cleaning, inspection, calibration and assists in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting. Handles raw materials per GMP and Safety requirements. Uses equipment such as pipettors, balances, osmometer, turbidimeter and pH meters. Ensure that tasks are performed in a safe and responsible manner to create an injury free and incident free workplace Required to follow through on assigned responsibilities and able to function under supervision. Responsible for promoting positive team environment through good communications and team engagement. May be required to work overtime. Performs other duties as assigned in support of business goals QUALIFICATION REQUIREMENTS: Minimum of High School Diploma or equivalent. Minimum of 6 months experience in a high-paced laboratory environment or manufacturing facility. Equivalent combination of education, training, and relevant work experience maybe considered. Must be able to read, write, and follow testing and inspection procedures. Must be able to maintain neat, accurate and complete records and logs. Mechanical aptitude and ability to disassemble and reassemble various equipment. Good communication skills and ability to work both individually and as part of a team. Flexibility with departmental work schedules including overtime. Must be able to focus with continuous attention to detail. Basic experience in weighing multiple components is required. Basic proficiency with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS Word and MS PPT is required. Statistical analysis using mathematical spreadsheets such as Excel or Minitab is highly desired. Must be able to lift or move approximately 40lbs 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.

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

Genefab is seeking an experienced analyst to join it's Quality Control Analytical group. In this role, you will support the GMP QC testing at GeneFab, with a focus on testing, method transfer, qualification, troubleshooting and investigations.Responsibilities Provide technical expertise (SME). Provide technical support to Analytical Development and QC Analytical Operations as needed. Develop, implement, and update all Quality Control SOPs, testing records and other documentation needed for cGMP compliance. Perform QC testing on in-process and final product samples to support release and stability testing. Lead and perform technical root-cause investigations for aberrant results and deviations relating to analytical methods. Lead and train junior employees to ensure testing procedures and practices comply with all applicable regulations and procedures. Plan, lead, and execute analytical method transfers, qualifications, and validations. Draft, Review, and Approve Method Transfer Protocols and Reports Generate and review procedures, protocols and reports. Proactively identify areas for continuous improvement in processes and procedures and lead these initiatives. Collaborate closely with Interdepartmental MSAT, ASAT, and Manufacturing groups to support, execute, and/or provide oversight in the execution of method optimization, characterization, troubleshooting, transfer, and qualification Perform additional duties as assigned Requirements B.S. degree in biology or related field with experience in cell therapy, immunology, cancer biology, or a closely related field. Minimum of 5+ years of GMP/QC Laboratory experience. Demonstrated ability to collaborate and work in cross-functional teams. Strong organizational skills and attention to detail Strong time management skills with a proven ability to meet deadlines Strong analytical and problem-solving skills Experience with relevant technologies such as: multicolor flow cytometry, cell culture (e.g., aseptic techniques, cell line expansion), multiplexed immunoassay, qPCR, and dPCR methods, Luminex, and ELISA. Experience in GMP. Experience with contract laboratories and or CDMO is a plus Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook record keeping (ELN) is a plus Proficient in MS Word, Excel, Project, and PowerPoint Experience with cell therapy or gene therapy is a plus Availability to work extended hours such as evenings or weekends to meet deadlines when necessary Comfortable in a fast-paced environment with minimal direction and able to adjust workload based on changing priorities Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the initial job description Able to lift up to 40 pounds $45 - $55 an hour About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Your Role at Baxter The Manufacturing Technician IV is responsible for assisting the supervisor in organizing, scheduling and directing other team members as well as execute all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Manufacturing Technician IV may be the main interface with other functional departments to resolve issues. Represent the department in cross- functional team as necessary. Your team: Baxter is focused on saving and sustaining lives by manufacturing high-quality products. We strive to create quality products for our customers each day. Delivering life-saving products is about getting them right, and attention to detail is how we make sure we meet that challenge. We are a team that supports each other throughout each shift. Working together in a supportive and open culture makes our processes evolve for the better and engages our workforce. What You'll Be Doing In-depth process knowledge of related manufacturing techniques and specialties. Perform and lead local manufacturing operations. Set up and operate general production equipment. Perform complex equipment troubleshooting and respond to process alarms as necessary. Support supervisor in reviewing relevant paperwork following GDP/GMP guidelines. Initiation and lead Continuous Improvement Teams. Receive and distribute supplies into the production area as necessary. Create and revise pertinent documentation as appropriate. Lead stretching exercises. Prepare and package product for shipment, where applicable. Train and mentor other team members and monitor training for newer team members. Collaborate with all other functional groups to ensure preventative maintenance is scheduled and completed. Print out and reconcile proper process documentation. Complete and closed GME and Maximo work orders Perform and lead cycle count and variance investigations. May perform other duties as assigned. What You'll Bring Requires High School diploma or GED equivalent with a minimum of 5-6 years of manufacturing related experience or AA degree with 3-4 years of manufacturing related experience required or Bachelor's degree with a minimum of 1 year of manufacturing related experience Must be proficient in written and verbal communication skills and understanding of cGMP regulations. Incumbent must be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurement. Must be able to read and follow detailed written instructions. Good interpersonal skills and be able to work effectively and efficiently in a team environment. This position requires shift, weekend and holiday work. Overtime may be required at times. The incumbent must work in a clean room/classified environment wearing special garments. Additionally, personal protective equipment and hand sanitizer must be worn due to safety requirements. Advanced knowledge of Microsoft Office/Word/Excel applications. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $60,000 - $82,500 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Know Your Rights: Workplace Discrimination is Illegal Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

**Job Title: Machine Operator** We are seeking a skilled Machine Operator to join our dynamic team. You will be responsible for the setup, sanitation, operation, and routine maintenance of capsulation machines, ensuring the production meets quality and safety standards. **Responsibilities** + Perform setup, sanitation, operation, and maintenance of capsulation machines. + Clean machines, equipment, and work areas using appropriate cleaning aids. + Ensure capsulation machines and areas are sanitary and report any issues to a supervisor. + Read work orders and Master Manufacturing Record to determine production specifications. + Pour, scoop, or dump specified mixtures into machines as per production requirements. + Adjust machine components to regulate speeds, pressures, temperatures, and material flow. + Perform test runs and examine sample capsules to ensure conformance to specifications. + Clean, oil, and make minor adjustments or repairs to machinery as needed. + Record production data including meter readings, quantities, and capsule specifications. + Transfer completed capsules to drying or storage areas, ensuring they are covered at all times. + Conduct ongoing assessment of quality control and operational procedures. + Meet or exceed production goals and guidelines. **Essential Skills** + High school diploma or equivalent with one to two years of related experience. + Strong organizational, problem-solving, and analytical skills. + Knowledge of production processes and quality control techniques. + Understanding of machine and tool designs, uses, repair, and maintenance. + Strong mechanical aptitude. + Good judgment with the ability to make timely and sound decisions. + Ability to follow written and verbal instructions and safety requirements. **Additional Skills & Qualifications** + Versatility and flexibility in adapting to changing priorities. + Ability to perform physical labor, including walking, kneeling, bending, standing, and lifting up to 50 pounds. + Ability to operate hand trucks, forklifts, and pallet jacks if required. **Why Work Here?** Join a team that values excellence and high standards. We offer a supportive work culture where your contributions are recognized. Our dynamic environment encourages growth and development, providing opportunities to enhance your skills and advance your career. **Work Environment** Work in a warehouse environment where temperatures can be cool to hot, and noise levels may vary from moderate to high. You will be required to wear protective gear such as gloves, face masks, and uniforms. The role involves exposure to small particles and odors. **Job Type & Location** This is a Contract position based out of Livermore, CA. **Pay and Benefits** The pay range for this position is $20.00 - $27.00/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 Livermore,CA. **Application Deadline** This position is anticipated to close on Dec 3, 2025. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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.

Working in collaborative group environment, we manufacture high quality custom oligonucleotides in a high efficiency, fast paced setting. These oligos manufactured are used in a variety of applications including helping perform genetic research, diagnose disease and help with food supply. What will you do? You work with a team to Manufacture Custom Oligonucleotides for use in the biotech industry by following established protocols and SOPs. The team uses semi-automated and automated basic lab equipment. Regularly evaluate non-routine test results and either fail the product or allow it to continue through the production cycle. Highly repetitive tasks for prolonged periods of time. Understand scientific principles in order to problem solve, troubleshoot test results, evaluate alternative choices and exercise independent judgment in selecting the best solution. Provide multiple decision options and corresponding logic/data behind the decisions. Proactively identifies production problems. Provides input and shares ideas and suggestions about improving lab techniques, protocols, processes, special handling of the product and equipment. Balance multiple tasks. Demonstrate knowledge in the use of basic lab techniques and basic computer knowledge. Demonstrate ability to meet standards as defined by the manufacturing process. Thoroughly and accurately complete documentation (completion of Batch Records, document data verifications, document problems, bring deviations to the attention of the Supervisor/Manager). Continuously strive to improve output goals. Demonstrate good time management resulting in efficiency. Support cost improvement initiatives by reducing failures, improving capacity and using supplies wisely. Reduce work in process, queues and cycle times. Advise appropriate people about problems/questions; be prepared to discuss problems/questions clearly. May be required to perform other related duties as required and/or assigned. Position occupies a significant role in mainstream oligonucleotide production. The role requires the ability to exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Skills Chemistry, Formulation, Gmp Top Skills Details Chemistry,Formulation,Gmp Additional Skills & Qualifications * Degree in the bench sciences (Biology, Chemistry, etc) is preferred but a HS diploma can be considered. * Strong digital literacy including familiarity with relevant software (Excel and Word) are required. * 1 year of lab experience preferred (1 year maybe acquired through work or school). * Proven track record of working well with others in a collaborative team environment. Knowledge, Skills, Abilities: * Operate in a fast-paced environment and while working as a team. * Efficient worker whom can multitask across multiple areas within the manufacturing environment. * Required to be able lift up to 20 lbs * Ability to stand while performing duties. * Capable of working safely with chemicals and hazardous materials. * Capacity to work outside of regular work hours when business demands call for it. Experience Level Intermediate Leve Job Type & Location This is a Contract position based out of Pleasanton, CA. Pay and Benefits The pay range for this position is $25.45 - $25.45/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 Pleasanton,CA. Application Deadline This position is anticipated to close on Dec 8, 2025. 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.

Work Schedule Third Shift (Nights) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materials Job Description Formulation Technician II 1st Shift: 6a-2:30pm PST Starting around $24/hr.! As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: The position is available at our Pleasanton site in California supporting the Genetic Sciences Division. How Will You Make an Impact?: The Pleasanton site is seeking a Formulation Technician II with interest in life sciences and biotechnology. The candidate will part of a manufacturing team for oligonucleotides and related products such as assays, arrays, and kits. A Day in the Life: Manufacture products as delegated by the Production Team Supervisor or Team Leader: Complete lab operations e.g. with automated systems like DNA/RNA synthesizers, liquid handlers, and with analytical instrumentation like HPLC and LCMS. Report metrics to the team leader during daily Tier Meetings and address and report any problems in and propose effective countermeasures. Education: High school diploma or equivalent required. Experience: Required: Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Preferred: Experience in a cGMP environment Knowledge, Skills, Abilities: Follow written SOPs and batch records and revise as needed. Perform manufacturing/ production tasks as scheduled. Handle and work with biological and chemical reagents. Maintains quality service by established organization standards. Ability to coordinate and prioritize work to ensure timely delivery. Communicate effectively with other production staff. Achieve high efficiency by reliable and punctual attendance. Physical Requirements / Work Environment Specific gowning is required including gloves, safety glasses with no makeup / jewelry, and hair, beard net and face cover for some operations. Ability to infrequently lift and manipulate up to 40 pounds unassisted. Ability to stand and move about including reaching, bending, stooping, grasping. Ability to use hand tools and equipment including forceful gripping, grasping, pushing, pulling and repetitive motion. Ability to use PPE (Personal Protective Equipment) and understand chemical hygiene including labels and SDS (Safety Data Sheets), common chemicals are disinfectant, solvents and IPA (Isopropyl Alcohol 70% and 99%). What We Offer Compensation Competitive Hourly Pay Rate Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays 401K Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities Compensation and Benefits The hourly pay range estimated for this position based in California is $21.42-$35.70. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Job DescriptionSalary: $23.00 - $25.00 per hour DOE Ideal Candidate Profile Do you fit this profile? Wants to start a CAREER / not just another "job" Wants to make a difference High Moral Standards & Values Positive Helpful Team Player Professional Wants to be the best of the best Is Ready Envirocheck is a growing company and has exciting opportunities for A players on our team. Job Summary Analysis of environmental samples for asbestos fibers, fungal spores, bacteria, and lead (Pb). Applicable equipment includes: A variety of microscopes, including Compound, Stereo, PLM (Polarized Light), and PCM (Phase Contrast). Flame Atomic Absorption Spectrometer IDEXX Colisure, Colilert, and Enterolert Microbiological media Requirements Bachelor's Degree in Biology, Microbiology, Geology, or related science Preferred Experience (not required, will train) Asbestos Analysis by PLM Fiber Analysis by PCM ISO 17025 Microscopes Excel programming is a plus Knowledge of construction (building) materials is a plus Benefits Health Insurance 401K with matching Paid sick / Vacation & Personal Time Paid Company Holidays

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

Formulation Technician II Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shifts: Monday to Friday from 07:00 AM to 03:30 PM Pay Rate: $23.00-$23.00/hourly Monday to Friday from 11:00 AM to 07:30 PM Pay Rate: $25.00-$25.00/hourly Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: This role is part of a collaborative manufacturing team focused on producing high-quality custom oligonucleotides in a fast-paced lab environment. The products support genetic research, disease diagnosis, and food supply applications. The position plays a critical role in mainstream oligo production, requiring sound judgment, adherence to SOPs, and continuous improvement mindset. Responsibilities: Manufacture custom oligonucleotides using established SOPs and protocols. Operate semi-automated and automated lab equipment. Evaluate non-routine test results and make pass/fail decisions or escalate appropriately. Perform highly repetitive tasks with consistency and accuracy. Troubleshoot test results using scientific principles and independent judgment. Proactively identify and report production problems. Suggest improvements to lab techniques, processes, and equipment handling. Balance and manage multiple tasks efficiently. Maintain thorough and accurate documentation (Batch records, deviations, data verification). Meet manufacturing output and quality standards. Support cost optimization by reducing failures and improving process efficiency. Work towards reducing WIP, cycle time, and process queues. Communicate issues clearly with supervisors and relevant stakeholders. Ensure adherence to safety guidelines while handling chemicals and hazardous materials. Collaborate effectively with team members and provide/receive performance feedback. Take on additional related duties as assigned. Required Skills: Degree in Life Sciences (Biology, Chemistry, or related field). 1+ year of lab experience (academic or industry). Prior experience in a manufacturing or production lab environment. Proven ability to work effectively in a collaborative team setting. Experience with high-throughput or repetitive lab workflows. Basic understanding of process improvement and lean manufacturing concepts. Knowledge of basic lab techniques. Strong digital literacy, especially MS Excel and MS Word. Ability to work in a fast-paced, high-volume manufacturing environment. Multitasking ability across different production areas. Good documentation and technical writing skills. Ability to stand for long periods and lift up to 20 lbs. Strong problem-solving and analytical thinking. Ability to follow SOPs and quality standards precisely. Comfortable working with hazardous chemicals and materials. Flexible to work shifts and extended hours when required. Team collaboration and communication skills. TekWissen Group is an equal opportunity employer supporting workforce diversity.

Battery Lab Technician - Failure Analysis & Materials Processing Energy Storage / Battery Technology Ultimate Staffing is seeking a highly motivated and detail-oriented R&D Technician to join our cutting-edge research team focused on advancing energy storage technologies. This role is pivotal in bridging theoretical innovation with practical experimentation, contributing directly to the development of next-generation battery systems for electric vehicles. Join a mission-driven team revolutionizing energy storage to enable a sustainable future. We are developing solid-state lithium-metal batteries designed to deliver longer range, faster charging, and enhanced safety for electric vehicles-supporting the global transition to a lower carbon future. This is a Monday-Friday -On-Site 9 am- 5 pm. Key Responsibilities: Collaborate with battery scientists and engineers on cutting-edge experiments. Independently execute steps in the cell failure analysis process. Support lab operations including metrology, materials processing, and equipment maintenance. Identify and troubleshoot issues with equipment and materials to improve cell processing. Contribute to the development and refinement of SOPs for improved efficiency and quality. Maintain inventory of lab supplies and ensure a safe, organized workspace. Accurately document lab activities and communicate daily results. Minimum Qualifications: High school diploma or equivalent. Ability to work in gloveboxes, Clean Dry Rooms, or fume hoods involving fine motor skills, standing, reaching, and lifting up to 15 lbs. One year or more of hands-on experience in a lab or process R&D environment. Strong attention to detail and commitment to high-quality results. Clear written and verbal communication skills. Enthusiasm for working in a fast-paced, collaborative environment. Preferred Qualifications: Experience with high-tech device assembly/disassembly. Familiarity with small microscope-scale products and tools such as VR-6000 optical profilometer, VHX digital microscope, and VK-X3000 3D Surface Profiler. Two years of experience in the battery industry. Background in battery fabrication, failure analysis, or materials processing. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Job Description Chemistry Lab Analyst Why Ascend? Come work for a company that is transforming the industry! We are Eurofins Ascend Clinical, LLC., one of the highest volume clinical laboratories in the United States. With the use of the most advanced tools and technology, we process millions of tests each month. For over 30 years, we have been delivering industry-leading service and excellence in testing. At Ascend, we are relentless about innovation and growing to pioneer the future of clinical and environmental laboratory testing. Ascend is unlike most companies, offering the discipline of a healthcare leader and the mentality of a tech startup. As a company that is on the leading edge, we are seeking individuals with a similar mindset who enjoy a dynamic, fast-paced environment. Job Summary The Chemistry Lab Analyst will perform moderate to high complexity testing on non-clinical specimens. Will operate and maintain highly complex instrumentations such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ion Chromatography (IC), as well as demonstrate proficiency on routine environmental testing, instrument maintenance and troubleshooting in accordance with protocols established by Ascend Clinical. Perform a variety of standardized microbiological tests such as heterotrophic place counts and endotoxin detection assay. Processes specimens, performs test preparation, specimen verification and tracking, all related clerical functions and general clean-up tasks for routine as well as high complex tests. Reports, analyzes, and verifies environmental results, which are substantiated by the proper use of quality control systems. Must recognize problems, identify causes and determine alternative methods and solutions. Actively contributes to quality assurance activities and participates in proficiency testing. Responsibilities: Knows and complies with all Ascend Clinical policies and procedures: General Policies, Chemical Hazard, Illness and Injury Prevention Program, Quality Assurance Program and ELAP. Understands the hazards associated with failing to follow those procedures Performs high complexity testing of water analysis according to EPA, AAMI, and/or ELAP guidelines Proficient in setting up multiple laboratory instrumentations used for non-clinical specimens Instrument daily, weekly, and monthly maintenance Troubleshooting instruments Instrument validation Attends and completes advance training for department instrumentations Capable of assisting in sample processing and preparation in high complex test environments Actively participates in facility's Quality Assurance program Assists in orientation and training of new staff members, as directed by management Assumes responsibility for special projects, as directed by management Oversees completion of maintenance records and workstation/instrument supplies. Ensures that regular preventive maintenance by the manufacturer has been completed Qualifications: College degree, science related preferred or equivalent number of years of relevant job experience 2-4 years of experience Proficient in chemistry, math, medical terminology, knowledge of specimen preparation techniques, and principles of operation of common laboratory instruments Knowledge of analytical techniques and high complexity instrumentation such as ICP-MS and IC Ability to follow complicated instructions with accuracy and perform detailed tasks thoroughly and completely Compensation: $25-35/hr Compensation may vary for different individuals in the same role based on several factors, including but not limited to individual competencies, education/professional certifications, experience and performance in the role Benefits: As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. Ascend is an Equal Opportunity Employer - M/F/Disabled/Veteran Eurofins Ascend Clinical, LLC is committed to promoting an equal employment opportunity workplace environment and is an equal opportunity employer. It is the policy of the company that all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship, pregnancy, genetic information (GINA), disability, military and/or veteran status, and/or any other status protected by applicable Federal, state, or local law. The company's policy is to recruit, hire, train, promote and administer all employment-related matters on the basis of an individual's qualifications, abilities and efforts without regard to protected status. Powered by JazzHR s3qDvPUViJ

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: 7: 00AM-3: 30PM Duration: 12 Months Pay range: $25.45 Hourly - $25.45 Hourly Onsite Job How will you make an impact? Working in collaborative group environment, we manufacture high quality custom oligonucleotides in a high efficiency, fast paced setting. These oligos manufactured are used in a variety of applications including helping perform genetic research, diagnose disease and help with food supply. What will you do? You work with a team to Manufacture Custom Oligonucleotides for use in the biotech industry by following established protocols and SOPs. The team uses semi-automated and automated basic lab equipment. Regularly evaluate non-routine test results and either fail the product or allow it to continue through the production cycle. •Highly repetitive tasks for prolonged periods of time. •Understand scientific principles in order to problem solve, troubleshoot test results, evaluate alternative choices and exercise independent judgment in selecting the best solution. Provide multiple decision options and corresponding logic/data behind the decisions. Proactively identifies production problems. •Provides input and shares ideas and suggestions about improving lab techniques, protocols, processes, special handling of the product and equipment. •Balance multiple tasks. Demonstrate knowledge in the use of basic lab techniques and basic computer knowledge. Demonstrate ability to meet standards as defined by the manufacturing process. •Thoroughly and accurately complete documentation (completion of Batch Records, document data verifications, document problems, bring deviations to the attention of the Supervisor/Manager). •Continuously strive to improve output goals. Demonstrate good time management resulting in efficiency. Support cost improvement initiatives by reducing failures, improving capacity and using supplies wisely. Reduce work in process, queues and cycle times. •Advise appropriate people about problems/questions;be prepared to discuss problems/questions clearly. Work in a safe manner. Work with team members to overcome obstacles. Collaborate, support and consult with other team members as necessary. Give and receive feedback about individual and group performance •May be required to perform other related duties as required and/or assigned. Position occupies a significant role in mainstream oligonucleotide production. The role requires the ability to exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. How will you get here? •Degree in the bench sciences (Biology, Chemistry, etc) is preferred but a HS diploma can be considered. •Strong digital literacy including familiarity with relevant software (Excel and Word) are required. Experience •1 year of lab experience preferred (1 year maybe acquired through work or school). •Proven track record of working well with others in a collaborative team environment. Knowledge, Skills, Abilities •Operate in a fast-paced environment and while working as a team. •Efficient worker whom can multitask across multiple areas within the manufacturing environment. •Required to be able lift up to 20 lbs. •Ability to stand while performing duties. •Capable of working safely with chemicals and hazardous materials. •Capacity to work outside of regular work hours when business demands call for it. •The above position will require you to work a flexible shift pattern. 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.