Quality control technician jobs in Novato, CA

A leading patent consulting firm in San Francisco is seeking a Patent Agent or Associate. The role requires a degree in engineering or related fields, registration to practice before the USPTO, and a law degree for attorneys. Candidates should be confident in discussing technical details and comfortable engaging with prominent tech companies. This position offers opportunities across various fields, including AI and clean energy. #J-18808-Ljbffr

Associate Analytical Technician About the Role As an Associate Analytical Technician, you will support manufacturing operations by conducting laboratory analyses that provide essential data for our processes. You will prepare samples, maintain laboratory instrumentation, acquire and report critical data, and help ensure accuracy and safety in our lab environment. Key Responsibilities Train under senior team members to perform routine laboratory analyses until proficiency is demonstrated Collect samples following defined Sample Plans Perform basic preventive maintenance of analytical systems and laboratory instruments Evaluate the validity of results for routine analyses and take necessary corrective actions Monitor analytical systems, escalating problems when required Document, communicate, and archive analytical results and related data Adhere to Environmental, Health and Safety (EHandS) procedures and Operating Discipline Management System (ODMS) practices Suggest improvements to laboratory processes and tools Escalate non-routine requests and issues to appropriate team members Requirements Education & Experience:Completion of Vocational Education or Upper Secondary Education (High School Diploma or equivalent) Laboratory, manufacturing, or related work experience preferred Coursework in chemistry or related scientific field (post-secondary education is a plus) Skills:Established basic laboratory skills Familiarity with standard operating procedures and analytical scientific methods Good communication and documentation abilities Attention to accuracy and safety standards Work Schedule Details:Workdays: 4 days on, followed by 4 days off (unless scheduled to cover vacation time) Shift Duration: 12-hour shifts Rotation: Every two weeks Day Shift: 5:50 AM - 5:50 PM Night Shift: 5:50 PM - 5:50 AM Example of Biweekly Rotation:4 consecutive day shifts (5:50 AM - 5:50 PM), followed by 4 days off Return for another 4 day shifts, then 4 days off Switch to 4 consecutive night shifts (5:50 PM - 5:50 AM), followed by 4 days off Continue with another 4 night shifts

Job Title: Lab Technician Pay Rate: $21.00/hr [Weekly Pay] Shift Timings: 06:00 AM to 03:30 PM [Monday to Friday] Contract Duration: 06 Months [Temp-To-Hire] Job Description: The Laboratory Technician will complete routine analytical and laboratory testing in support of the food safety quality and operational teams. Perform routine analysis of product testing, being responsible for checking and monitoring instrumentation performance and conducting tests. Document results into databases and/or communication test results. Help develop food/feed safety, quality and regulatory culture collaborating cross-functionally to build, maintain and improve an effective food safety, quality and regulatory culture. Run calibration checks, preventive maintenance tasks, and simple repair to analytical instrumentation, maintaining customer specifications books up-to-date. Interpret and document results of tests into active databases and communicate results to internal customers as required.

Performs any combination of the essential duties and responsibilities of quality control at manufacturing facility in Dixon, CA. Successful candidates will be required to participate in a pre-employment drug screen and random drug screening per our Drug Free Workplace policy. Dependability for work schedule is crucial. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Inspects cast floats, float assemblies, and metal fabrications, hardware components, and lumber; * Inspects the casting process per drawing requirements; * Performs concrete tests per ACI / PCI and customer specifications; * Scans production and inspection documents; * Conducts safety tasks and inspections as required by The BMI Safety Program; and * Documents and records QC activities. * Performs other duties as assigned. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE: High school diploma or equivalent required. Requires knowledge of or ability to learn the characteristics of concrete float fabrication with 12 months of experience working with concrete and/or prior inspection. Requires one year of experience in Quality Control. CERTIFICATES, LICENSES, REGISTRATIONS: ACI concrete field testing tech Grade 1 Certification. Possess or ability to obtain PCI Quality Control Technician Levels 1 and 2 within 12months of hire. Ability to read production drawings. COMPUTER SKILLS: To perform this job successfully, an individual should be proficient with MS Word, MS Excel, and MS Outlook. Must be able to use a document scanner.

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in Corporate Sector, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Conduct in-depth reviews of existing processes for effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations. Lead development & implementation of formal processes, procedures, workflow automations to continuously optimize the team's resources to improve reliability, costs, and sustainability. Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals. Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work. Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance. Develop and execute comprehensive project plans, incorporating technical requirements, resource allocation, and timelines to ensure on-time delivery of technology solutions Required qualifications, capabilities, and skills Formal training or certification in Information Technology, and/or 5+ years of technology, risk and controls knowledge. Strong leadership skills with exceptional communication and presence Advanced knowledge of multiple IT control and project management practices and experience working across large environments Ability to collaborate with high-performing teams and individuals throughout the firm to accomplish common goals Experience In Depth reviews of existing processes for effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations. In-depth knowledge and experience in Infrastructure and/or Application Risks and Controls Ability to independently use systems and analyze/use data to address/identify gaps in Controls, and highlight Risk Working experience in collaborating with engineering as well as business functions to achieve objectives and hold difficult conversations/escalations Preferred qualifications, capabilities, and skills Demonstrated ability to multi-task in a high-pressure environment Fast learner with an eye for detail CRISC, CISSP, or other industry-recognized risk certifications are preferred Audit experience preferable, but not mandatory

Job DescriptionSalary: $24-$34 DOE General Description OMW is a highly respected contract manufacturing company specializing in precision machining of custom metal and plastic parts for some of the worlds largest aerospace, electronics, and healthcare companies. We have recently been ranked one of the Top 100 Fastest Growing Private Companies in the Bay Area, by the San Francisco Business Times. The Fast 100 List will be featured in a special print edition of the San Francisco Business Times. To support our rapid growth, we are looking to fill new positions and are looking for team members who are challengers, teammates, strategic thinkers, customer-oriented achievers, and game changers with a desire to create a long term partnership with OMW. Experience Required: Must have Excellent written English skills and ability to read and write reports and documentation. Direct machining or manufacturing experience in aerospace and avionics highly desirable. CMM programming experience is highly desirable. Experience and aptitude using windows PC software, including Excel and Word. Some background in Quality Management Systems such as ISO 9001 & AS9100 is a plus. Knowledge of Basic GD&T principals. Skills required: The ability to use calipers, micrometers, pin and thread gages, height gages, microscopes, comparators, and other measurement equipment (training available). Must be able to operate automated CMM after training and prepare FAIR documentation. Ability to read engineering prints and interpret tolerancing and dimensions (including geometric tolerancing). Weekend Shift is a full-time position and has flexible hours. The Shift must cover Saturday and Sunday, but other days are flexible. For the weekend schedule, we currently offer two options: a 3-day shift covering 12 hours each day, or a 4-day shift covering 10 hours each day. Specific Responsibilities: Prepare FAIR and other QC documentation. Operate and program CMMs for quality inspections (can train). Prepare shop floor inspection reports and perform first article inspections on in-process parts. Perform final QC signoffs and inspections on completed parts. Keep parts from "escaping" with unacceptable defects. Work to continuously lower company's defect rate. Handle customer and internal non-conformances. Interface with company's software systems. Compensation based on experience. Benefits include 100% company paid healthcare for the employee (85% for family), generous paid time off accrual, retirement plan with company contribution, educational support, bonuses, and more. Please email your resume or job history to email provided in header. Suitable candidates will be contacted for interviews. This position requires use of information or access to production processes subject to national security controls under the U.S. export control laws and regulations (including, but not limited to, the International Traffic in Arms Regulations (ITAR) and the Export Administration Regulations (EAR)). To be qualified to work for OMW Corporation, a successful applicant must be a U.S. Person, as defined in those regulations, and able to supply evidence of that qualification prior to starting work. The U.S. export control regulations define a U.S. Person as a U.S. Citizen, U.S. National, U.S. Permanent Resident (i.e., Green Card Holder), and certain categories of Political Asylees and Refugees. OMW Corporation is an equal opportunity employer and drug-free workplace.

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $25.20 - $34.65 Job Purpose The Quality Control Technician receives raw materials and performs product inspection and/or audits in accordance with established quality control program. This role involves sampling and testing of incoming raw materials to ensure that they, along with in-process and finished products meet the company's quality standards Responsibilities · Receive and perform inspection of incoming raw material/components to ensure compliance with company quality standards · Perform visual inspections on sub-assemblies and finished good products to identify defects and non-conformances · Maintain product quality by adhering to data management protocols · Support efficient supply chain operations by complying with and maintaining inventory control procedures · Ensure compliance with internal quality control standards and external regulations, and continuously improve quality control processes · Assist in the development and implementation of quality control procedures. · Collaborate with production teams to address quality issues and recommend corrective actions Qualifications Education: · High School Diploma · A.A Degree a plus Skills and Experience: · Life Sciences industry experience preferred. · Experience working in a Quality Control environment is strongly desired. · Previous experience performing incoming inspections is strongly desired. · Detail-oriented, efficient, and excellent organization skills. · Excellent verbal and written communication skills · Strong team player with the ability to work independently. · Able to multi-task and prioritize. · Proficiency in Microsoft Office and other relevant software · ISO and GMP experience preferred Working Conditions: · Significant amount of time on the production floor, in a laboratory setting · Some time in an office setting documenting inspection result, analyzing data, and communicating with team members Physical Requirements: · Standing and walking · Lifting and moving materials up to 50 pounds · Use of hands for precises tasks such as handling samples and testing equipment Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Quality Technician will report to the Receiving Quality team lead and have the final goal to support the development of business processes to ensure that Ryzen's Client's products and services provide a high level of quality that meets the defined standards and specifications and in the end, the customer expectations. You will be helping in establishing high quality standards and will ensure product quality standards are met through inspection, documentation, and process improvement activities across receiving quality operations. You will support quality management systems by conducting audits, performing root cause analysis, and implementing corrective actions while collaborating with cross-functional teams to maintain high-quality standards in manufacturing and services. In this role you will: Perform part and vehicle level quality inspection to ensure the product is meeting specifications. Process incoming material and validate conformance to established quality standards Document various procedures and work instructions Support creating and reporting metrics to demonstrate quality status in NPI, manufacturing, and services Enter test result data into SAP and JIRA systems Help in Root Cause Analysis activities, Corrective Action implementation and validation Support process improvement activities Work with cross-functional teams as needed Qualifications Bachelor's degree with 6- 8 years of experience in the manufacturing environment (automotive, semiconductor, or aerospace fields are preferred). Experience in performing Quality inspections based on control plan Experience with Root Cause Analysis, Problem Solving and Quality Control methods Must be familiar with Google suites (words, docs, sheets) Strong planning, organizational, analytical, interpersonal, decision-making, oral and written communication skills Bonus Qualifications Electrical component (wire harness) inspection experience Previous experience in SAP and/or JIRA system Industry background and/or experience in; automotive, software, contract manufacturing, customer management Pay Rate: $35.00/HR - $45.00/HR

Design Quality Technician The Design Quality Technician -CMF will report to the Design Quality Team Lead and will be responsible for ensuring the visual and aesthetic quality of CMF (Color, Material, Finish) components meets design intent and defined quality standards. This role plays a key part in maintaining the highest quality standards for interior and exterior appearance parts through inspection, documentation, and continuous improvement activities. The technician will support the Design Quality and receiving organization by performing detailed color and material inspections, verifying visual harmony across components, and coordinating with suppliers and cross-functional teams to resolve quality issues and uphold brand standards. In this role, you will: Perform visual inspections of CMF parts to ensure compliance with specifications and design intent. Evaluate color, texture, gloss, and material harmony across multiple materials and components. Identify, label, and organize CMF samples and parts for inspection and shipment. Support supplier quality by returning nonconforming samples and documenting findings. Maintain inspection records, images, and data within Google Sheets, Docs, and shared databases. Collaborate with Design, Manufacturing, and Supplier Quality teams to resolve appearance-related issues. Utilize tools such as spectrophotometers or colorimeters to quantify color differences when applicable. Support root cause analysis and corrective action validation related to visual or CMF quality concerns. Qualifications: Bachelor's with 6-8 years of experience in a manufacturing or quality environment (automotive industry preferred). Demonstrated experience in color discrimination and color harmony evaluation. Ability to evaluate and compare color across multiple materials (plastic, metal, fabric, paint, etc.). Ability to lift to 50 pounds. Strong attention to detail and visual accuracy. Experience with basic data entry and documentation using Google Docs, Google Sheets, and other digital tools. Excellent organizational skills and the ability to manage multiple tasks with minimal supervision. Preferred Qualifications: Hands-on experience using spectrophotometers or colorimeters. Experience organizing and managing CMF sample libraries. Familiarity with automotive design quality or CMF processes. Goal-oriented mindset with strong communication and teamwork skills. Experience working with cross-functional teams including design, quality, and manufacturing. Previous experience in SAP and/or JIRA system Schedule: Monday to Friday from 8am - 5pm

Dragonfly Group is an experienced hybrid real estate solutions company focused on providing an integrated system of properties, technologies, and services designed to improve the real estate experience for all. Dragonfly Group currently has more than 40 operating investment entities throughout the Bay Area. Vert, a member of the family of Dragonfly Group companies, is modernizing the home design process by developing modular, panelized homes to reduce construction time while introducing innovative construction methods and materials. Vert's light-gauge-steel based modular building system streamlines the production process while infusing smart technology (Adomi) into its homes to enhance the experience of the homeowner. Vert seeks an experienced Quality Control Inspector to perform routine quality inspections and tests. Successful candidates will be meticulous in their work, detail-oriented, and possess a background in quality processes. Must be knowledgeable about measurement and test equipment (MT&E). Aptitude for working with data and a solid grasp of basic engineering concepts are helpful. Excellent interpersonal and communication skills are a must. We're looking for a highly organized, methodical professional with a proven track record of experience and success. We offer competitive salaries and an excellent opportunity for career development. Responsibilities: Vert's Quality Control Technician reports to the Quality Control Manager. Perform quality inspections and tests accurately and efficiently, both in the factory and at construction sites, using a variety of instruments, tests, and calculations to determine conformity to the required standards. Inspect and ensure supplies received at the factory or construction sites meet quality standards and consistency. Identify defects in workmanship or non-compliance to specifications and standards. Monitor other accountable individuals carrying out quality activities. Compare test results for compliance with company and regulatory requirements, record results, and notify management of out-of-specification tests and trends. Monitor manufacturing quality at control checkpoints throughout the manufacturing process and identify deviations from control limits-both in the factory and at the construction sites. Correctly record and file all relevant record logs and documentation using databases and systems. Work with cross-functional teams to monitor and improve quality, reliability, and performance. Support, calibrate, and run automated quality control systems. The above duties and responsibilities are representative of the nature and level of work assigned and are not necessarily all-inclusive. Qualifications: High School Diploma/GED - required 1+ years in quality control or quality assurance position Meticulous attention to detail Must have excellent math skills; ability to add, subtract, multiply and divide by all units of measure-using whole numbers, common fractions and decimals. Excellent interpersonal skills Experienced with software, including Word and Excel Skilled with measurement and test equipment Good verbal and written English

3rd Shift QC Lab Tech needs 4 years experience QC Lab Tech requires: 10p-630a Tues-Sat High school diploma/GED and experience working in a chemical laboratory preferred. PC proficiency in Microsoft Office products, specifically excel tabling and charting, SAP, and other database experience preferred. Familiar with analytical equipment, wet chemistry techniques, and/or mechanical testing apparatuses. Strong work ethic, self-motivated and ability to drive projects to desired results. Ability to work on requested shift. Training rotations may occur on a different shift than the application states, and can take 1-3 months to complete. QC Lab Tech duties: Complies with all Safety, Health, and Environmental rules, procedures and regulations. Conducts all laboratory work in a safe manner including the use of proper Personal Protective Equipment (PPE), adherence to the site safety practices, use of lab equipment, 5S, etc Perform all work in strict adherence to QC standard laboratory procedures (SLPs). Reviews and provides recommended improvements to QC standard laboratory procedures (SLPs). Inspection and testing of incoming raw materials, semi-finished goods, and finished goods according to defined instructions, procedures and methods. Executes lab testing and generates test data, documentation and lab reports. Communicates basic observations regarding data and/or experimental outcome. Provides support for projects assigned by Engineers and/or Supervisors. Assists in maintaining project timelines. Employs basic problem-solving skills to overcome project bottlenecks and maintain project deliverable dates

Full-time Description To assist in Inspection Lab activities allowing it to perform seamlessly while providing accurate, repeatable measurement results that fully support the needs of our internal and external Customers Requirements 1) Working with peers to help coordinate and schedule Inspection Lab functions so all requirements are accomplished in the most efficient manner possible. 2) Perform first piece, in-process, and final inspections and document as required 3) Program and operate the CMM & Faro Arm 4) Crosstrain on all lab equipment to have a functional knowledge and operational ability of the equipment listed above 5) Be a subject matter expert on the use of all conventional measuring equipment, ability to design and develop specialty gauging, along with a highly developed understanding of GD&T 6) Work with the QA Manager and Quality Engineer and other Inspectors to perform capability studies, Gauge R&R studies, and other statistical techniques. 7) Supply the necessary data for AS9102 and PPAP submissions. 8) Assist in calibration activities to ensure all are accomplished as scheduled Research, and suggest upgrades/alternatives/additions to the existing lab equipment while also justifying the procurement by demonstrating the appropriate ROI

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Quality Control Technician part time contract position for 6 months. Quality Control Technician needs: High School graduate and two years of college chemistry or related science courses Minimum of 2 years experience as a Lab Technician in a business setting is highly desired. Demonstrated proficiency at routine mathematics, which includes addition, subtraction, multiplication and division. Experience with basic tool manipulation including mixing equipment, lab glassware, testing machines, and other standard lab tools. Quality Control Technician duties: Laboratory Technician is responsible for the daily activity of specimen preparation, evaluation, and data generation for certification reporting of adhesive and composite products in either of two laboratories Additional Information $22//hr 6 months

QC/QA Technician - Job Description The QC/QA Technician is responsible for ensuring that products meet company quality standards and regulatory requirements throughout all stages of production. This role performs routine inspections, testing, documentation, and verification activities to support consistent product safety, quality, and compliance. Key Responsibilities Conduct quality checks on raw materials, in-process products, and finished goods to ensure they meet established specifications. Perform routine line inspections-including temperature monitoring, labeling verification, seal integrity, weight checks, and coding accuracy. Collect, record, and maintain accurate quality data in accordance with company, customer, and regulatory guidelines. Monitor GMPs (Good Manufacturing Practices) across production areas and report deviations or non-conformances promptly. Assist with root-cause investigations, corrective actions, and continuous improvement initiatives. Calibrate, operate, and maintain laboratory or quality testing equipment as required. Collaborate with production, sanitation, and management teams to support a safe and compliant manufacturing environment. Ensure adherence to food safety, quality policies, and regulatory standards such as FDA, USDA, HACCP, or SQF (as applicable). You should be proficient in: Food Safety and Quality Assurance (FSQA) Basic Computer Skills

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: *****************************************************

General Description OMW is a highly respected contract manufacturing company specializing in precision machining of custom metal and plastic parts for some of the world's largest aerospace, electronics, and healthcare companies. We have recently been ranked one of the Top 100 Fastest Growing Private Companies in the Bay Area, by the San Francisco Business Times. The Fast 100 List will be featured in a special print edition of the San Francisco Business Times. To support our rapid growth, we are looking to fill new positions and are looking for team members who are challengers, teammates, strategic thinkers, customer-oriented achievers, and game changers with a desire to create a long term partnership with OMW. Experience Required: Must have Excellent written English skills and ability to read and write reports and documentation. Direct machining or manufacturing experience in aerospace and avionics highly desirable. CMM programming experience is highly desirable. Experience and aptitude using windows PC software, including Excel and Word. Some background in Quality Management Systems such as ISO 9001 & AS9100 is a plus. Knowledge of Basic GD&T principals. Skills required: The ability to use calipers, micrometers, pin and thread gages, height gages, microscopes, comparators, and other measurement equipment (training available). Must be able to operate automated CMM after training and prepare FAIR documentation. Ability to read engineering prints and interpret tolerancing and dimensions (including geometric tolerancing). Weekend Shift is a full-time position and has flexible hours. The Shift must cover Saturday and Sunday, but other days are flexible. For the weekend schedule, we currently offer two options: a 3-day shift covering 12 hours each day, or a 4-day shift covering 10 hours each day. Specific Responsibilities: Prepare FAIR and other QC documentation. Operate and program CMMs for quality inspections (can train). Prepare shop floor inspection reports and perform first article inspections on in-process parts. Perform final QC signoffs and inspections on completed parts. Keep parts from "escaping" with unacceptable defects. Work to continuously lower company's defect rate. Handle customer and internal non-conformances. Interface with company's software systems. Compensation based on experience. Benefits include 100% company paid healthcare for the employee (85% for family), generous paid time off accrual, retirement plan with company contribution, educational support, bonuses, and more. Please email your resume or job history to email provided in header. Suitable candidates will be contacted for interviews. This position requires use of information or access to production processes subject to national security controls under the U.S. export control laws and regulations (including, but not limited to, the International Traffic in Arms Regulations (ITAR) and the Export Administration Regulations (EAR)). To be qualified to work for OMW Corporation, a successful applicant must be a U.S. Person, as defined in those regulations, and able to supply evidence of that qualification prior to starting work. The U.S. export control regulations define a U.S. Person as a U.S. Citizen, U.S. National, U.S. Permanent Resident (i.e., “Green Card Holder”), and certain categories of Political Asylees and Refugees. OMW Corporation is an equal opportunity employer and drug-free workplace.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Training period is 1st shift and then need to be flexible to work on different shifts- Quality Control Technician with minimum of 2 years experience as a Lab Technician. Quality Control Technician requires: High School graduate and two years of college chemistry or related science courses Demonstrated proficiency at routine mathematics, which includes addition, subtraction, multiplication and division. manipulation including mixing equipment, lab glassware, testing machines, and other standard lab tool computer skills to manipulate and graph data and report experimental work Quality Control Technician duties are: Analyzes and interprets test results and determines acceptability Records time spent against work orders Must follow all applicable policies, procedures and guidelines. This includes the safe and proper operation of any/all applicable machinery and equipment Additional Information $22/hr 6 months

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.