Tech Patent Counsel & Prosecution for Engineers
Quality control technician job in San Francisco, 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.
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Formulation Technician I
Quality control technician job in Sunnyvale, CA
Formulation Technician I
Duration: 12 Months
Job Type: Temporary Assignment
Work Type: Onsite
Shift: Monday to Friday from 02:00 PM to 10:30 PM
Pay Range: $20.00 to $25.00/hr.
Overview
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below 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:
Work in a team-based manufacturing lab environment within the Chromatography and Mass Spectrometry Division (CMD) in Sunnyvale, CA. Responsible for synthesizing and testing ion exchange media used in chromatography consumables.
Responsibilities:
Test resin products on specialized instruments to meet customer demand.
Record and report test results accurately and maintain proper documentation.
Complete production work orders according to established procedures.
Follow corporate quality policies to ensure high-quality standards.
Follow safety requirements and actively participate in safety improvement activities.
Maintain a clean and organized laboratory environment.
Required Skills:
High school diploma or equivalent.
Previous work experience in manufacturing, operations, production, or a lab setting or related field.
Knowledge of Good Laboratory and Manufacturing Practices and standards.
Good mathematical, problem-solving, and organizational abilities.
Excellent verbal and written communication skills.
Ability to read and understand written procedures (SOPs) and follow verbal instructions.
Familiarity with commonly used hand tools (wrenches, torque drivers, tweezers, etc.).
Proficiency with spreadsheet and database software.
Ability to lift and/or move up to 40 pounds.
Ability to sit, stand, walk, and use hands/fingers to handle and feel small components.
Visual ability to detect small components and particles.
TekWissen Group is an equal opportunity employer supporting workforce diversity
Technical Engineer
Quality control technician job in San Jose, CA
Russell Sigler Inc. is a leading independent distributor in the HVAC industry, specializing in Carrier products for over 50 years. Our mission is to deliver exceptional service and products while fostering a supportive work environment for our employees.
Position Summary:
The Technical Engineer provides design, systems application, and proposal preparation. Works with outside sales engineers, territory managers, and customer contracting and engineering accounts. Responsible for a variety of tasks including equipment selection, job pricing, creation of bid projects, producing submittals, placing orders, and other key job responsibilities including but not limited to the following:
Key Duties and Responsibilities:
Provide high-level independent ownership of projects of varying size at the different stages of execution, sometimes from start to finish including design, vetting, bidding, submittals, and final release of order
Read, interpret, and make pricing and technical equipment selections, and decisions based on contract documents, including but not limited to engineering specifications, engineered equipment schedules, and architectural/engineering plans
Review of engineering design and contractual documents to identify areas of risk and compliance
Utilize mechanical engineering to verify mechanical equipment is being applied and implemented within the intended and acceptable range of operation
Estimating and proposal writing of complex commercial engineered equipment and automation projects
Technical specification writing and review
Design and application support of external consulting engineering firms for commercial and industrial construction projects
Project site visits for engineering and application support of commercial equipment and automation.
Offsite project and opportunity meetings with contractors, engineers, owners, and complementary trades
Management of multiple time-sensitive deadlines simultaneously
Coordinate between the contracting sales department and engineering sales department on design changes and strategy
Interact and work closely on a daily basis with outside sales engineers, territory managers, engineering firms, contractors, owners, project coordinators, central bid desk, credit department, order entry department, customer assurance department, warehouse employees, and manufacturers
Provide independent high-level direct support for certain contractors, engineers, and outside sales engineers
Coordination and verification of multiple external vendors and internal departments to create complex single-package equipment and automation solutions
Work among a team to complete a large array of projects in varying phases, delegating work among each other, and independently completing
Participate in the development and maintenance of standard operating procedures
Attend and participate in job meetings, sales meetings, and trainings
Participate in the training of others within and outside of the department
Self and group leadership of technical development training and education
Critical Knowledge and Skills:
Accuracy, analytical skills, and attention to detail are required
Exceptional communication and customer service skills
Detail oriented
Multitasking and organizational skills
Good judgment and planning skills
Work independently with minimal supervision in a fast-paced work environment
Research using systems, software and product guides, catalogs, and manufacturing literature
Review, evaluate, and make suggestions and product recommendations to customers as well as provide technical support when needed
Knowledge of HVAC Carrier Products is preferred
Knowledge of Carrier software (Quote Builder, Sage, HVAC Partners, ECAT, vendor websites) is preferred
Work in a constant state of alertness and a safe manner
Education and Experience:
BS in Engineering is required, a Mechanical Engineering degree is preferred
Must have a minimum 3-5 years of HVAC industry and sales experience
Pay Range:
Starting at $70,000.00 annum.
** Russell Sigler, Inc. (Sigler) is an equal opportunity employer. All applicants will be considered for employment based on merit, qualifications, and business need **
Inventory Control Technician
Quality control technician job in San Jose, CA
Johnson Service Group has an immediate temporary opening for an Inventory Control Technician for our client in San Jose. This position is responsible for performing a variety of warehouse and inventory control tasks, including receiving, sorting, and distributing materials, tools, supplies, and equipment. Duties include operating material handling equipment for loading and unloading shipments, supporting internal mail delivery, and ensuring the timely and safe delivery of requested materials to various offices on campus.
Key Responsibilities
Receiving and Sorting: Unpack materials, supplies, tools, and equipment. Verify articles received against packing lists and purchase orders.
Inspection: Inspect incoming materials for wear, damage, or defects; count or weigh articles and notify appropriate staff if repairs or adjustments are required.
Issuing Materials: Fill orders from requisition forms. Issue tools, parts, and other technical materials and equipment in compliance with established policies and procedures.
Material Handling: Operate a variety of material handling equipment, including delivery trucks/vans and forklifts, to load and unload equipment and supplies.
Inventory Management: Operate a computer system to access inventory and related information. Apply code numbers to materials and equipment from an existing code system and label items for storage.
Skills:
Organization
Customer service
Strong problem-solving skills
Courier experience
Working independently with minimal supervision
Perform a variety of inventory control functions
Maintain records and files
Qualifications
High school diploma or equivalent.
Minimum of one year of storekeeping or inventory control experience.
Proficiency in using computers. Ability to operate material handling equipment.
Valid California Driver's License
Must obtain client Forklift Certification within six (6) months of appointment.
Rate 32.43/hr.
Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.
Plating Process Technician
Quality control technician job in Milpitas, CA
TITLE: PLATING PROCESS TECHNICIAN
FLSA STATUS: NON-EXEMPT
A SHIFT: MONDAY THRU WEDNESDAY AND EVERY OTHER THURSDAY 6:00 AM TO 6:00 PM
REPORTS TO: DIRECTOR, PLATING PROCESS ENGINEERING
Under the direction of the Director of Plating Process Engineering, the Plating Process Technician provides support to the engineering teams in the plating area, including assisting with wet etch process, preparing and maintaining recipes, reviewing and documenting process or procedures, and expediting and dispositioning prototype wafers; maintains process controls using Statistical Process Control (SPC), collects and analyzes data, and recommends corrective action. This position is located in Milpitas, California.
ESSENTIAL FUNCTIONS:
Provides support to the engineering teams in the plating, wet etch, and stripping process areas
Supports the plating, wet etch, and stripping processes by preparing, maintaining, and setting up recipes to ensure an efficient and consistent process
Reviews and documents processes and procedures; partners with engineering to implement changes effectively
Expedites and dispositions prototype wafers in the plating, wet etch and stripping areas
Assists engineers to run plating process development experiments, collects and analyzes data, and recommends corrective action if required
Reviews and maintains process controls using SPC and prepares charts and graphs
Assists with routine trouble-shooting and resolves basic process-related issues
Participates in and recommends modifications to procedures or processes in support of continuous improvement initiatives
Collaborates with Engineering to qualify or approve new processes or procedures
Creates reports, charts, or graphs on an ad-hoc or routine basis
Prepares daily pass down report for engineers, next shift plating process technicians, and manufacturing plating technicians
Responds to inquiries from other team members, managers, or departments
Adheres to all safety policies and procedures as required
Performs other duties of a similar nature or level*
MINIMUM QUALIFICATIONS:
Associates degree in Electronics or Industrial Technology and/or equivalent relevant experience
Two years of experience working in the semiconductor industry
Knowledge of plating, wet processes and procedures
Hands on experience using metrology tools such as pH meter, Tencor Thickness Profiler, XRF, and B-H loop tools
Proficient in the use of Microsoft Office Applications
Required Knowledge, Skills, and Abilities:
Knowledge of semiconductor or hard disk drive (HDD) principles and processes
Knowledge and ability to use SPC to maintain process controls
Knowledge of plating, wet processes and procedures
Ability to collect and analyze data, present findings, and recommend corrective action
Ability to adhere to all safety policies and procedures
Ability to communicate effectively with all levels of employees and management
Demonstrated ability to follow routine verbal or written instructions
Demonstrated problem solving and organizational skills
Demonstrated time management and prioritization skills
Skilled at resolving issues quickly and efficiently
Flexible and able to prioritize
The hourly rate for this full-time position is between $25.00-$40.00 + bonus target + benefits. Within the range the individual pay may differ depending on additional factors including job responsibilities, job related knowledge, skills, abilities, education, and experience. The hourly pay range shown is subject to change and may be modified periodically.
WORKING CONDITIONS:
The Plating Process Technician works primarily in an indoor environment on A shift which is Monday thru Wednesday and every other Thursday 6:00 AM to 6:00 PM. The schedule may be altered from time-to-time to meet business or operational needs; may travel from building-to-building as needed. Works in a class 100 ESD sensitive wafer manufacturing facility; wears a cleanroom (bunny) suit, including hood, gloves, safety glasses, booties, and mask. May be exposed to hazardous conditions, chemicals, fumes, and/or gases during the course of work day; Stands and walks; performs various fine grasping movements, bends, and twists; operates a computer and enters information using a keyboard, operates a telephone, and other office equipment. Must be able to load and unload various wet etch chemical solutions several times per shift. May be required to push, pull, or lift up to 25 pounds.
*Other duties of a similar nature or level are duties that may be required, but may not be specifically listed in the job description or posting.
TDK/Headway Technologies, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, national origin, age, disability, or genetics. Applicants requiring accommodation in order to complete the application process should contact the Headway Human Resources Department.
Laboratory Technician
Quality control technician job in Hayward, CA
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
Laboratory Technician
Quality control technician job in Newark, CA
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.
Tech Risk and Controls Lead
Quality control technician job in San Francisco, CA
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
Auto-ApplyManufacturing FAB/QC Tech
Quality control technician job in Santa Clara, CA
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, 8services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek- so they can do what they do best: improve the world around us. Information about Agilent is available at ****************
Essential Responsibilities:
This is a 12-hour Variable shift. Performs Micro Array process, which includes, but is not limited to, Writer/synthesis, deprotection, dicing of wafers using standardized tooling, QC Processes/OLS Cleaving documentation and procedures.
Performs troubleshooting and verifies that the product conforms to customer specifications.
Maintains accurate reports and provides necessary documentation.
Helps implement process/product improvements, etc.
Additionally, the new hire will be expected to support both Manufacturing Fab and QC operations within 12 months to enhance flexibility and support across functions.
This role follows a 12-hour variable shift schedule (5:00 PM - 5:00 AM), working Thursday evening through Sunday morning, with every other Wednesday included in the rotation.
The above statements are intended to describe the general nature and level of work being performed by incumbents. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required by all incumbents. Incumbents may perform other duties as assigned in addition to the above. All Agilent employees are expected to: Promote teamwork and cooperative effort. Help train and give guidance to other Agilent employees. Maintain a clean, safe, and unobstructed work area, practice good safety habits, and utilize appropriate safety equipment. Provide customers with the highest quality products and service. Understand and apply appropriate quality improvement and Processes.
Qualifications
Ability to use basic math applied to the job.
Ability to communicate both verbally and in writing.
Computer skills on Windows-based applications such as MS Word, Excel, and Outlook.
Ability to set up and operate Micro Array Manufacturing machines, preferred.
Must be comfortable working around chemicals.
May be able to demonstrate the ability to lift materials per entity-specified and approved limits.
Desirable: Higher education.
Experience Team Leadership.
Familiarity with Lab instruments such as LCMS, HPLC, etc., preferred
MES, Agile, and SAP experience.
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least September 15, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $30.03 - $46.93/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: NoShift: MorningDuration: No End DateJob Function: Manufacturing
Auto-ApplyQuality Technician
Quality control technician job in Hayward, CA
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
Formulation Technician
Quality control technician job in Sunnyvale, CA
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.
Quality Technician III
Quality control technician job in San Jose, CA
TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering and systems integration. Our tightly integrated offerings are tailored to each clients requirements and span the services spectrum from Application Development/Maintenance, testing, IT Consulting & staffing for IT Infrastructure Management through strategic consulting and industry oriented Business Process. Our end-to-end Business Process as a Service (BPaaS) solutions support complex, high-value, knowledge based work. Combining applications, platforms, infrastructure, knowledge processes, and domain expertise allows us to deliver greater efficiencies and innovative business capabilities.
Qualifications
Position:Quality Technician III
Location:San Jose,CA
Pay Rate : $30.00 - $35.00/hr.
Essential Duties & Responsibilities:
* With limited supervision, assures policies, procedures, inspection techniques and quality plans conform to established standards
* Performs complex analyses and tests of raw materials, packaging materials and/or finished products from manufacturing to ensure quality standards and compliance to customer and regulatory requirements
* Monitors performance of inspectors and institute corrective action when necessary
* Trains new inspectors and department personnel on policies, procedures, inspection techniques and quality plans
* Assures gauges are within the current calibration cycle and are properly used and stored. Arranges for repair of gauges as needed.
* Participates in design of experiments and process capability studies
* Reviews Statistical Process Control (SPC) data. Maintains integrity of SPC data by correcting input errors and follows up with retraining of inspectors if needed.
* 4+ years related experience and/or training
* Experience certifying typical metrology equipment such as calipers, micrometers and computer controlled gauging equipment
* General knowledge of blue prints, engineering specifications interpretation, inspection using measuring and test equipment, including CMM, FARO ARM and measurement techniques, geometric dimensioning and tolerance and quality calibration processes required.
Additional Information
If you are available, interested, planning to make a change, or know of a friend who might have the required qualifications and interest, please call me ASAP at ************
Thanks & Regards,
Monika
Quality Technician - Weekend
Quality control technician job in Novato, CA
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.
Quality Control Inspector (swing shift)
Quality control technician job in Santa Clara, CA
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
Formulation Technician
Quality control technician job in Livermore, CA
**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.
Quality Technician
Quality control technician job in Fairfield, CA
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
Formulation Technician II
Quality control technician job in Pleasanton, CA
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.
Formulation Technician II -1st Shift
Quality control technician job in Pleasanton, CA
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: *****************************************************
Auto-ApplyFormulation Technician II
Quality control technician job in Pleasanton, CA
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.
Formulation Technician
Quality control technician job in Sunnyvale, CA
Shift: Monday -Friday with overtime and weekend hours as needed Duration: 12 Months Pay range: $23.00 Hourly - $23.00Hourly Onsite Job How Will You Make an Impact? Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables.
A Day in the Life:
Testing of resin products on specialized instruments to meet customer demand.
Record and report test results accurately and maintain proper documentation.
Complete production work-orders according to established procedures.
Follow corporate quality policy to ensure high-quality standards.
Follow safety requirements and actively participate in safety improvement activities!
Maintain a clean and organized laboratory environment.
Education:
High school diploma or equivalent required.
Experience:
Required: No previous work experience required
Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field
Knowledge, Skills, Abilities:
Knowledge of Good Laboratory and Manufacturing Practices and standards.
Good mathematical, problem-solving, and organizational abilities.
Excellent verbal and written skills
Ability to read and understand written procedures (SOPs) and follow verbal instructions.
Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.)
PC literate and have experience with spreadsheet and database software.
Physical Requirements / Work Environment
Lift and/or move up to 40 pounds.
Regularly required to sit, stand;walk;use hands & fingers to handle & feel.
Visual abilities to detect small components and particles.
Exposure to toxic or caustic chemicals, fumes or airborne particles.
Occasionally exposed to moving mechanical parts and moderate noise level.
PPE requirements: lab coat, Safety glasses, gloves, face shields, & safety shoes (all company provided.)
P95 Mask in the areas that have exposure of solvent fumes.
Employee Benefits:
At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits:
Four options of medical Insurance
Dental and Vision Insurance
401k Contributions
Critical Illness Insurance
Voluntary Permanent Life Insurance
Accident Insurance
Other Employee Perks
About LanceSoft
LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.