Manufacturing technician jobs in San Rafael, CA

Title: Manufacturing Specialist Pay: $25.00-$31.00/hour Duration: 6-Month Contract Schedule: 1st Shift (8-hour days; flexible start between 6:00 AM - 8:00 AM) Job Description Position Summary: This role provides technical and process support to the manufacturing team to ensure production goals are met while maintaining quality, efficiency, and compliance with established quality systems. Key Responsibilities Analyze production data to identify trends and recommend actions that improve efficiency, product quality, and cost. Identify process gaps and collaborate with engineering teams to drive improvements. Support validation activities as a subject matter expert, including reviewing validation plans, executing protocols, and ensuring validated state is maintained. Serve as an SME for MES and eDHR systems; collaborate with cross-functional teams during development and change management. Create, update, and support Quality Documents such as SOPs, work instructions, pFMEAs, test methods, batch record templates, and validation reports. Participate in continuous improvement initiatives using Lean and Operational Excellence methodologies. Contribute to internal audit activities and assist with corrective actions and audit responses. Test next-generation instrumentation using approved procedures. Troubleshoot product non-conformances and work closely with Manufacturing, Quality, and Life Cycle Management to resolve issues. Maintain reports tracking instrument failures and defects. Perform other duties as assigned. Required Education High School Diploma or GED. Some college-level STEM coursework or related technical training preferred. Preferred Background & Skills Bachelor's degree in Engineering, Chemistry, Biology, Physics, or related field preferred. No prior technical experience required; detailed instructions will be provided. Strong organizational skills and attention to detail. Ability to work both independently and collaboratively in a team environment. Strong communication and troubleshooting skills. Proficient with Microsoft Office (Excel, Word, PowerPoint). Experience with SOPs, DHRs, ECOs, GLP, GMP, and SAP is a plus. Hands-on experience with diagnostic or sequencing instrumentation is highly desirable.

Manufacturing Technician - Fremont, CA (On‑Site) Pay: $47.00/hour. Schedule: Full-time, Monday-Friday, 8:00 AM-4:30 PM Work Environment: In-person. Some travel to Hayward as needed An on-demand autonomous ride‑hailing company is seeking a Manufacturing Technician to support the assembly and testing of next‑generation autonomous vehicles. This team is transitioning from R&D to commercial launch, and your hands-on expertise will directly influence build quality, system reliability, and production readiness. You'll work on vehicle assembly lines, support sub‑assemblies, run software bring‑up scripts, perform light diagnostics, and collaborate closely with engineering teams. Your feedback will help refine processes, improve safety, and accelerate the company's path to mass production. What You'll Do Work closely with leads and technicians on vehicle assembly line builds Perform sub‑assembly of smaller components to support production Support bring‑up activities, including running scripts and assisting with software testing Conduct light diagnosis and troubleshooting of vehicle issues Execute daily tasks to ensure on‑time project completion Provide feedback to engineering and development teams Collaborate with cross‑functional teams as needed Follow all Environmental Health and Safety (EHS) guidelines Identify opportunities to improve quality, efficiency, and safety Ideal Candidate Profile The strongest candidates bring hands‑on mechanical skills, a positive attitude, and the ability to stay productive even during downtime. Positive attitude, quick learner, strong team player Comfortable with cutting, drilling, teardown, and rebuild work on Toyota Highlanders Experience with sub‑assembly to feed the production line Able to run basic software scripts (copy/paste, execute) Bachelor's degree + 4-6 years experience preferred; 2-4 years considered with strong soft skills Electrical work is minimal (10-15%) and can be learned CAN/LIN familiarity is a plus Automotive line experience translates well Semiconductor line experience is not a fit Required Skills & Qualifications Bachelor's degree with 4-6 years of technician or manufacturing experience, or equivalent industry experience Proficiency with basic hand and power tools Strong analytical and problem‑solving skills Understanding of basic electrical theory Ability to read electrical schematics and harness drawings Familiarity with CAN/LIN systems is a plus Automotive/OEM experience preferred Associate Degree or Certificate in Automotive Technology is a plus Why This Role Matters As a Manufacturing Technician, you'll help build and test autonomous vehicles equipped with Gen2 technology. Your work will directly influence: Build quality System reliability Safety improvements Speed to commercial launch Your hands-on insights will help refine key systems and accelerate the company's transition from prototype to production.

CLEANROOM PACKAGING OPERATOR Location: Palo Alto, CA Reports to: Operations Manager Shift: Days Compensation: $19 - $23/hr We've built our reputation as an industry leader by delivering world-class precision metal finishing solutions for over 50 years. We proudly serve a variety of industries including aerospace, defense, medical, semiconductor, and other high-tech industries that demand uncompromising quality and reliability. Our team is dedicated to craftsmanship, innovation, and exceeding customer expectations - every component, every time. Your Role: As a Cleanroom Packaging Operator, you'll be part of the final stage of production, preparing finished parts for shipment in a controlled environment. You'll handle wrapping, sealing, labeling, and boxing while maintaining the organization and cleanliness required for high-quality work. What You'll Do: Package finished metal parts in a cleanroom environment following established procedures. Wrap, seal, label, and box items with accuracy and efficiency. Maintain organization and cleanliness in the packaging area. Inspect parts for visible flaws or irregularities before packaging. Follow quality and safety standards at all times. Assist with other production tasks as needed. What You'll Bring: Basic packaging or manufacturing experience preferred. Strong attention to detail and ability to follow instructions. Self-motivated with a positive attitude and willingness to learn. Organized, reliable, and comfortable working in a fast-paced environment. Commitment to cleanliness and quality standards. Outstanding teamwork and communication. Must meet US person status due to export regulations.

• Follow and execute established reliability test procedures and perform various environmental, mechanical, and certification testing • Photographic documentation of test setup and results • Set up and run test equipment • Record, analyze, and report test results using spreadsheets, charts, and slides • Operate thermal chambers for temperature and humidity testing • Provide timely updates on testing progress • Responsible for several tests and products throughout the development life cycle • Responsible for the safe operation of test setups • Responsible for proper use of lab equipment (only ones they've been trained to use) Develop and Execute Test Plans: Design and carry out comprehensive reliability test plans (e.g., thermal cycling, vibration, shock, humidity, burn-in, life testing) for new and existing products or equipment to simulate real-world operating conditions. Failure Analysis & Root Cause Determination: Conduct detailed failure analyses (FA) and root cause analyses (RCA) for failures identified during testing or in the field, implementing effective corrective actions and permanent solutions. Reliability Modeling & Prediction: Use statistical methods and software tools (e.g., Weibull analysis, Design of Experiments (DOE), FMEA) to predict future performance, model failure rates, and assess potential risks. Collaboration: Work closely with design, manufacturing, quality assurance, and maintenance teams to provide key input on "Design for Reliability" (DFR) and "Design for Maintainability" principles. Documentation & Reporting: Compile data, generate detailed reports, and communicate test results, findings, and recommendations to cross-functional teams and management

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

Senior Optics Assembly & Test Technician Walnut Creek, CA Compensation & Benefits Pay: $100-150,000 annually with monthly and annual bonuses Medical, dental, vision with 401(k) match, FSA, Life insurance, Paid time off Relocation assistance Monday thru Friday 8:00am - 4:30pm Overview We're looking for a highly skilled technician to assemble, align, and test precision optical and opto-mechanical components. This work involves handling very small, delicate parts-lenses, mirrors, windows-and using a range of optical tools and test equipment. The role is hands-on, detail-heavy, and critical to delivering high-performance optical products. This role requires access to ITAR/EAR-controlled information. Candidates must be a US Citizen or US Permanent Resident. What You'll Do Assemble precision optical and opto-mechanical components using fixtures, hand tools, and test instruments Align and install optical elements while monitoring performance specs Operate and maintain optical test equipment (interferometers, profilers, centration tools) Perform detailed test procedures to verify product functionality Troubleshoot and repair complex assemblies that fail testing Clean and inspect optical parts under a microscope Read and follow work instructions, engineering drawings, and schematics Document production steps, test data, and results accurately Maintain a clean, safe workspace (including possible cleanroom work) Partner with engineering teams to provide feedback and support process improvements What You'll Need Education: Experience with Optics: 5+ years High school diploma or GED required Associate degree or technical certificate in Optics, Photonics, Electronics, or related field preferred Experience: 5+ years working with optical, fiber-optic, or semiconductor assemblies in a manufacturing or lab setting Technical Skills: Strong hand-eye coordination and fine manual dexterity Skilled with precision hand tools and optical metrology equipment Basic understanding of optics, physics, mechanics, and electronics Comfortable using computers for testing and documentation Soft Skills: Excellent attention to detail Strong troubleshooting and problem-solving abilities Clear communication skills Ability to work independently and as part of a team Physical Requirements: Ability to inspect parts under a microscope Fine hand/finger manipulation Able to sit, stand, kneel, or bend for extended periods Lift up to 35 lbs If this sounds like a great fit - please reach out for a conversation!

Primary Duties & Responsibilities * Performs hands-on operation of optical dicing process * All optical sizing steps performed per procedure to a 0% reject standard. * Quality of product and throughput rate meets or exceeds departmental goals. * Products meet quality per internal and external customer specifications. * Works with the team to meet delivery goals * Improve processes under the guidance of supervision. * All steps are performed per policy and procedure * Follow instructions and procedures closely * Learn, understand and follow all applicable safety and environmental regulations * Responsible for maintaining Quality work environment housekeeping for own work area and community areas * Adapts readily to changes in work caused by new requirements and/or situations * Openly communicates with team Education & Experience * High School diploma or equivalent * Basic reading and math skills (add, subtract, multiply, divide) Skills * Capable of applying basic math to product activities * Ability to understand and interpret product drawings (blueprints) * Ability to meet tight time schedules * Familiarity with precision optics manufacturing and metrology * Work in environment with open communication * Perform tasks independently with minimal guidance from supervisor * Ability to follow work priorities and multi-task when needed * Good interpersonal and communication skills * Set a high standard of ethics, professionalism, and competency * Demonstrates and promotes the II-VI Worldwide values: Customer First; Honesty and Integrity, Open Communications, Teamwork, Continuous Improvement and Learning; Manage by the "Facts"; A Safe, Clean and Orderly Workplace Working Conditions * Indoor, stand / sit processes Physical Requirements * Able to stand / walk for long periods of time Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. * Learn, understand and follow all applicable safety and environmental regulations * Responsible for maintaining Quality work environment housekeeping for own work area and community areas Quality and Environmental Responsibilities * Work in environment with open communication * Perform tasks independently with minimal guidance from supervisor * Ability to follow work priorities and multi-task when needed * Good interpersonal and communication skills * Set a high standard of ethics, professionalism, and competency Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

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Keysight is at the forefront of technology innovation, delivering breakthroughs and trusted insights in electronic design, simulation, prototyping, test, manufacturing, and optimization. Our ~15,000 employees create world-class solutions in communications, 5G, automotive, energy, quantum, aerospace, defense, and semiconductor markets for customers in over 100 countries. Learn more about what we do. Our award-winning culture embraces a bold vision of where technology can take us and a passion for tackling challenging problems with industry-first solutions. We believe that when people feel a sense of belonging, they can be more creative, innovative, and thrive at all points in their careers. Responsibilities Keysight Technologies is hiring full-time equipment technicians for a semiconductor manufacturing facility. This position is at our Santa Rosa, California site, located in the wine country, about one hour north of San Francisco. Santa Rosa is a medium-size city of 175,000 people, with a mild climate and many recreational opportunities. Keysight in Santa Rosa is a product development site and has many technically challenging jobs. We design and build test instruments for RF/microwave communications, 5G, and autonomous vehicles. Keysight culture values teamwork, collaboration, work/life balance, diversity and inclusivity. Keysight has been voted a Great Place to Work four years in a row. Job Description: Maintenance Technician to Support IC Manufacturing in Semiconductor Fab Work with R&D semiconductor equipment in Keysight's High Frequency Technology Center Wafer Fab. Maintain and repair electro-mechanical equipment that may use high vacuum, sub-micron precision, exotic chemistry, advanced imaging, and many other state-of-the-art manufacturing techniques. Work closely with process engineers and operators to aid in both volume production and R&D process development. Work with suppliers to select and purchase spare parts, and to coordinate service visits. Perform preventative maintenance and emergency repairs in a manufacturing environment. Work closely with our Equipment Engineering team to: Assist in the retirement of legacy tools Develop written maintenance procedures Install new process tools Develop PM and repair procedures and determine spare parts requirements Assist with implementing hardware improvements and automation projects. Qualifications Minimum Requirements: Maintenance experience with manufacturing equipment or other complex systems. Familiarity with Microsoft Office suite of tools and standard engineering practices. Strong personal and e-mail communication skills. Proven ability to manage multiple responsibilities simultaneously and solve complex problems independently. Ability to learn on the job and work with cutting edge technologies and processes. Desire to work in a highly technical organization with a very strong and inclusive team. Ideal candidates for this position would possess some of the following attributes: Previous experience maintaining semiconductor equipment or complex manufacturing hardware AS/BA/BS degree in Electronics, military electronics training, or strong electro-mechanical technical capability. Previous experience working across disciplines including mechanics, electronics, materials science, and software engineering. Experience with semiconductor manufacturing techniques is highly desired. Experience with high vacuum technology, deposition methods, different etching technologies and RF sources. Pay Range: USD $67,030.00 - USD $111,720.00 Year Note: For other locations, pay ranges will vary by region This role is eligible for Keysight Results Bonus Program US Employees may be eligible for the following benefits: Medical, dental and vision Health Savings Account Health Care and Dependent Care Flexible Spending Accounts Life, Accident, Disability insurance Business Travel Accident and Business Travel Health 401(k) Plan Flexible Time Off, Paid Holidays Paid Family Leave Discounts, Perks Tuition Reimbursement Adoption Assistance ESPP (Employee Stock Purchase Plan) Restricted Stock Units Visa Sponsorship is unavailable for this position Careers Privacy Statement***Keysight is an Equal Opportunity Employer.***

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Essential Technician : Operate systems that clean and sterilize tanks and filtration systems. Prepare solutions for the production process. Review documentation and check all calculations (e.g. tickets, labels, equipment reading). Trouble shoot equipment and process problems. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Use of automation to perform production operations. Provide support to Manufacturing to meet production demands. Operate automated systems for equipment operation. Assemble and prepare equipment for production. Exhibit detail oriented documentation skills Communicate effectively and ability to work in a team environment. Exhibit professional interpersonal skills. Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues. Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Job Matrix A good working knowledge of biopharm technology and processes. Trained and skilled in all operational procedures of at least one manufacturing department. Demonstrated ability to independently document and record information related to the process. Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems. Recognizes non-routine problems, investigates and suggests potential solutions. Judgment is required in resolving problems and making routine recommendations. Ability to recognize deviation from accepted practices is required. Supplementary Responsibilities : Operate bioreactors, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up) Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Qualifications Degree in Life Sciences or engineering and 1 year related experience Or Associate Degree and 3 year experience Or High school and 5 years' experience Biotech certificate from approved program Additional Information Sneha Shrivastava Sr Technical Recruiter 862 - 579 - 4236

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: Purifies proteins in a regulated FDA licensed and ISO certified facility and performs cross-functional activities associated with downstream production runs in collaboration with Bulk Fill and QC testing groups. The role may include special projects such as process development and validation activities where scientific research principles are applied. Primary responsibilities: Purify recombinant proteins to ensure commercial product demands are met: 1. Works as part of the purification team to perform purification, filtration, and centrifugation operations according to standard operating procedures. 2. Executes laboratory operations including dispensing of chemicals, volumetric and gravimetric measurements, making accurate dilutions, and preparing solutions. 3. Performs SAP duties that include cycle counting, reservations, issuing to process orders, and charging of expiring raw materials. 4. Performs equipment preventative maintenance tasks, column packing, and column testing procedures. 5. Ability to multi-task and become proficient at purifying 14 different proteins and make conjugates. 6. Responsible for ordering raw materials and components, as required. 7. Maintains a safe and well-organized work environment and complies with safety procedures. Follow regulatory requirements: 1. Adheres to valid manufacturing procedures, manufacturing operations, and current good manufacturing practices (cGMP) and ISO requirements. Documentation: 1. Responsible for the completion and review of batch records and logbooks, which requires legible, clear, and concise data entry. 2. Completes all training documentation within a pre-defined timeframe. Analytical Testing: 1. Analyzes in-process samples generated from purification activities. 2. Operates lab equipment such as pH meters, balances, centrifuges, spectrophotometers, HPLC systems, and densitometers. Skills:Must have an understanding of protein purification processes. • Experience following and writing instructions. • Very good verbal and written communication skills. • Computer knowledge required with experience using MS Word and Excel. • Able to document work accurately and has excellent organizational skills. • Experience with preparation of reagents following instructions. • Delivers quality products and services on time to all customers. • Must be attentive to detail. • Effectively manages time. • Considers how all daily manufacturing activities impact product quality. • Monitor processes and products to identify opportunities for continuous improvement. • Able to lift and push up to 35 lbs. 1. Works well in a team environment to manufacture production lots. 2. Complies with cGMP and ISO requirements. 3. Maintains accurate documentation related to manufacturing processes. Education:BA/BS in the sciences (Biology, Engineering, or related field) or 2 years of relevant experience Languages:English Read Write Speak Additional Information Best Regards, Anuj Mehta ************

@HYVE Solutions, missions to help customers, business partners, and employees achieve success through shared goals, strategies, resources and technology solutions. Hyve Solutions is a leader in the data center solutions industry, designing, manufacturing, and delivering custom Server, Storage, and Networking Solutions to the world's largest Cloud, Social Media, and Enterprise companies. We pride ourselves on collaboration, innovation and thought leadership. Our team consists of diverse, forward-thinking individuals who dare to challenge the status quo, while working with many of the world's biggest customers. Hyve Solutions is a part of Synnex Corporation, a Fortune 500 company. Become part of a team that thrives on excellence in a fast changing, high-growth technology environment! Hyve Solutions is looking for a detail-oriented, hands-on, results-driven individual with proven communication skills and a strong work ethic to work in a challenging, fast-paced, energetic environment. Responsibilities: · Perform troubleshooting, repair, preventative and general maintenance on production tools and equipment · Work with vendors to troubleshoot and resolve equipment issues · Build and install tools and equipment to support factory requirements · Support Process Engineering team on programs and projects · Document equipment and tools issues, maintenance records, tooling logs and asset recording · Order parts and supplies to support production · Provide day to day tool and equipment support to production · Work with Production and Process Engineering to determine and recommend tool and equipment needs · Provide training to production and Process Engineering personnel as needed Qualifications: · Typically requires 2+ years of related experience and Associates degree or 4 years of related experience · Proficient in MS/Office (Word, Excel, etc.) · Mechanical aptitude, good with tools and working with your hands · Ability to lift 25lbs consistently · Work with precision tooling in small places · Understanding of general safety guidelines and practices · General knowledge of electro-mechanical functionality · Excellent communication skills Hyve Perks Every Day is Casual Day • Company Discounts • Community Involvement Opportunities • Profit Sharing • Medical, Dental & Vision Insurance • 401k • FSA & HSA • Paid Vacation, Holiday & Sick Days • Employee Stock Purchase Plan • Tuition Reimbursement • Live Well Work Well Program • And More The preceding job description has been designed to indicate the general nature and level of work performed by employees with this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. @ HYVE Solutions, we believe employees are our greatest asset and we empower them to make a difference in our business. Diversity and inclusion make us all better. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.

Proterra offers a dynamic and supportive workplace where our employees can thrive personally and professionally. With cutting-edge facilities and groundbreaking projects, Proterra offers unique opportunities to grow, collaborate, and lead transformative change in the electrification of heavy-duty transportation and equipment. Our commitment to innovation extends beyond our battery solutions to our people, where we create an environment where everyone feels valued, supported, and empowered to drive change for the earth. Here at Proterra we strive to foster a culture of inclusivity, valuing diverse perspectives and encouraging bold ideas, allowing our employees to bring their full selves to work. Our employees benefit from competitive total rewards packages, and opportunities to develop professionally. Position Overview This position as part of the Advanced Manufacturing Engineering (AME) organization will be responsible for supporting building battery prototypes within the Battery Engineering organization, the design and development of novel manufacturing equipment and processes to develop new battery pack designs. The Advanced Manufacturing Engineering Technician is responsible for working with engineering teams to develop and tune processes. They will also build new equipment and fixtures to specification. The role will include collaboration with both internal and external partners, taking a hands-on role ensuring that the factory can achieve the required capacity of batteries to be used by Proterra's customers. About the Role - You will: * Lead technician work and operations relates to building and troubleshooting new equipment and manufacturing fixtures, setting up prototype builds, and testing new manufacturing processes. * Maintain and uphold high safety standards * Support the Advanced Manufacturing Engineering team in building complex mechanical and electrical assemblies * Support the development of processes and equipment to allow Proterra to build prototypes and prepare battery pack design for production launch * Fabricate and/or modify existing prototype components/fixtures * Execute Process Studies to help engineers determine best process parameters for a given manufacturing process * Work from engineering drawings and specifications to create fixtures and equipment * Provide feedback and suggestions to new and/or improved equipment and processes * Keep the lab space clean, organized, and equipped with supplies or machines * Collaborate with sustaining engineering and maintenance teams to train them on specialty equipment * Other duties as assigned by management About Our Group: * The Advanced Manufacturing Engineering group seeks to develop innovative new manufacturing processes and automation tools to establish Proterra as a world leader in battery pack manufacturing. It is comprised of several different teams focused on different aspects of battery manufacturing, including process development and automated manufacturing equipment design. * This role is part of the larger Battery Technology Team. The Battery Technology Team's work is guided by our team values: * INNOVATION: We think of new ideas and take bold action to bring them to life. * ADAPTABILITY: We react quickly to our ever-changing environment. * CONTINUOUS IMPROVEMENT: We strive to make our products, services, and processes better. * TEAMWORK & COLLABORATION: We work together to solve problems with camaraderie. * INCLUSION: We create welcoming spaces where everyone can bring their whole selves to a diverse work community. * SUSTAINABILITY: We change the world through environmentally responsible practices. * KINDNESS: We are honest, caring, and respectful with each other. * You will report to the Sr Manager, Advanced Manufacturing Engineering within the Battery Engineering Organization and collaborate with other team members located at our R&D headquarters in Burlingame, CA and manufacturing facilities in Greer, SC. About You: * Self-starting individual with the ability to adapt interpersonal styles and techniques to influence at all levels of the organization * Customer-focused attitude, with high level of professionalism and discretion. * Ability to maintain strict confidentiality, establish trust and credibility, and act with complete integrity. * Detail-oriented, resourceful and diligent. * Flexible and open to change * Strong time management and organizational skills; proactive and the ability to work with little supervision. * Sound judgment and problem-solving skills; challenge assumptions not supported by engineering analysis * Ability to prioritize tasks and manage multiple priorities simultaneously. * Excellent written, verbal, and presentation communication skills * Ability to travel as needed to Proterra and project-related partner sites * Ability to travel as needed to Proterra and project-related partner sites Your Experience Includes: * Associate degree in related field or at least 8+ years of relevant experience such as: * Car mechanic * Manufacturing line associate * Troubleshooting mechanical/electrical systems * Other technical troubleshooting, test or manufacturing environments * Experience managing shop operations such as checking in on other technicians' progress, reporting out status updates to management, organizing materials and tools to increase productivity * Demonstrated understanding of schematics, assembly drawings, and mechanical drawings * Demonstrated knowledge of basic workshop etiquette, provide verbal and written communication across all teams * Working knowledge of computers and Microsoft Office products * Proficiency with mechanical fabrication tools such as drill presses, saws, mills, hand tools, etc * Physical Demands: * May work various shifts as needed; may be requested to travel to different locations. * Lifting up to 25 pounds and occasionally 50 pounds. * Able to walk, stand, crouch, bench, kneel, lift, carry and reach as needed in large and tight spaces. * Good eye/hand coordination and ability to identify color variations, depth perceptions and close or distance visual items. * Manual dexterity with occasional repetitive finger motion. * Environmental Demands: * Ability to work in manufacturing environment with extreme heat and cold conditions. * Wear protective clothing or respiratory protective equipment. * Works with irritant chemicals, gases, etc. You Might Also Have: * Experience as an engineering technician or process * Experience with relevant technologies such as sensors, electronics, controls, pneumatics, valves, and mechanisms * Electrical and mechanical assembly experience: crimping, cabinet builds, cable routing, soldering * Machining and fabrication experience with manual milling machines, welding of steel assemblies Base Location: Burlingame, CA Common Travel Locations: Greenville, SC; Vendor Sites Travel: 0-20% Compensation: $50/hr - $60/hr Applicants must be authorized to work for any employer in the U.S. There is no immigration sponsorship available for this role (ex: H1-B, OPT, CPT, TN or any other employment sponsorship). Proterra is an Equal Employment Opportunity Employer, providing equal employment opportunities to all Employees and applicants for employment without regard to race, color, creed, religion, sex, sexual orientation, gender identity, national origin, disability, age, genetic information, veteran status, pregnancy, childbirth, or related medical conditions, including, but not limited to, lactation or any other characteristic protected by applicable federal, state, or local law or ordinance. Proterra participates in the Electronic Employment Verification Program (E-Verify). #LI-BJ1

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.

Located in the heart of Silicon Valley, Tenergy is a total power solution provider in the rechargeable battery and renewable energy industry. With over 20 years of reputation and track record, Tenergy is a recognized leading battery brand and Power solution partner in the fast growing renewable energy sector. Tenergy serves broad spectrums of customers for their applications including consumer electronics smart devices, industrial application, medical, electrical transportation and power storage. The application and business possibility with our products is endless with increasing needs for mobility and durable power. Tenergy offers competitive products in the market due to our global logistics, scale, quality, and commitment to customer satisfaction. Job Description The candidate will work in a team work environment, perform battery testing and battery charging duties, may assemble small size battery packs and related sub-assemblies when needed. Candidate must be a team player with demonstrated skills and abilities, or the fast learner in assembly manufacturing, material handling, soldering, wiring and ability to comprehend basic prints and wiring diagrams. The candidate may perform a variety of tasks in accordance with their training, experience, and skill as assigned by their Lead or Supervisor including: Assemble small size battery packs and related sub-assemblies according to specifications and drawings. Spot soldering and welding for electrical board (PCB). QC Testing and RMA analysis. Perform battery testing according to the defined procedures. Perform battery charging according to defined operating procedures. Perform proper data recording. Report issues and troubleshooting issues identified during the testing. May assist with new battery pack design. May assist with existing battery pack design improvement. Qualifications College degree in engineering Attention to details and responsible work attitude Excellent hand-eye coordination, hands-on, manual dexterity Ability to read/listen carefully to follow instructions and procedures Team player with good communication, interpersonal skills Ability to use common sense to solve practical problems. Electrical-related knowledge and training are plus. Experience in electrical assembly and soldering is a plus. Additional Information Salary DOE $20-$23/hr. Eligible for Medical/Dental/Vision Insurance and 401K with company match, paid holidays. Work schedule is Monday- Friday 8:30am-5:00pm.

Job Description TITLE: Manufacturing Engineering Technician COMPANY SUMMARY: Imagine a world where you could bring the precision and control of surgery to catheter-based therapies. For decades, endovascular procedures have been constrained by the technological limitations of catheters that lose stability and control within the anatomy. We have created a new class of therapies to overcome these constraints by using Endoportal Control to mimic the precision and control of direct surgical access, while maintaining the minimally invasive profile of an endovascular intervention. Our vision is big, spanning the breadth of cardiovascular disease where we see compelling opportunities to reimagine therapies for millions of patients. Jupiter Endovascular is a medical technology startup located in the San Francisco Bay Area, led by a team of successful medical device entrepreneurs. We have big ambitions, with a culture built on innovation, teamwork, and speed. We have raised capital from a diversified investor base, including venture capital, private equity, and corporate strategic investors. POSITION SUMMARY: As a Manufacturing Engineering Technician, you'll be a pivotal member of the manufacturing team, supporting production of innovative medical devices for the treatment of cardiovascular disease. Reporting to the Manufacturing Engineering Manager, the Manufacturing Engineering Technician plays a critical role in maximizing production uptime by maintaining, troubleshooting and monitoring production processes, equipment, fixtures, and tooling used in the manufacturing and assembly of finished medical devices. The role will be responsible for all site equipment used in production and new product development, including laboratory equipment. This role partners closely with manufacturing engineers, quality, operations, and production personnel to ensure production safety, quality, reliability, and efficiency goals are met. The role will also support continuous process improvement, process development, process validation, process transfer and other new product introduction activities. We're seeking a passionate, high-energy professional who thrives in a medical device startup environment and can deliver on the responsibilities below. This is an in-office role. ROLES AND RESPONSIBILITIES Provide ongoing technical support for production equipment and manufacturing assembly processes. Maintain performance of production equipment, fixtures and tooling. Troubleshoot equipment and process issues to minimize production downtime. (mechanical, electrical, HMI/GUI). Perform preventive maintenance, calibration, and repairs. Create and maintain accurate equipment logs and records in compliance with QMS. Set-up and test production equipment, fixtures and tooling. Maintain accurate process and inspection documentation (MPI, QIP). Train production manufacturing assemblers on manufacturing process instructions, equipment set up, testing and regular cleaning and maintenance. Create spare parts list, maintain spare parts inventory to ensure availability and minimize downtime. Perform installation and installation qualification (IQ) for equipment spares. Remediate and maintain production equipment documentation in compliance with equipment SOPs. Identify product quality process risks and collaborate with engineers to implement mitigations. Identify and recommend process and operational efficiency improvements (throughput, yield, cycle time, etc.). Collaborate with engineers to implement improvements. Support production data collection (SPC) and data monitoring. Support implementation of lean six sigma manufacturing initiatives (e.g. - 6S, visual management). Troubleshoot and maintain performance and calibration of laboratory equipment and maintain laboratory equipment log. Assist manufacturing engineers with activities related to new product development, validation and new product introductions; to include setting up pilot lines, new equipment introduction, and executing design of experiment (DOE), process capability studies, process validation protocols (OQ, PQ), software validation, and engineering builds. Support new product introduction (NPI), process transfer and production ramp up. REQUIRED QUALIFICATIONS Required Minimum Education: High school diploma. Required Minimum Experience: 3+ years of manufacturing engineering technician or equivalent (medical device experience preferred). Experience troubleshooting, maintaining and calibrating production equipment, fixtures and tooling. Experience following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and safety protocols (OSHA). Hands-on experience with adhesive bonding and UV curing processes. Contributed to the improvement of manufacturing processes and process documentation. Ability to effectively communicate in English (verbal and written). Proven ability to work independently with a given set of priorities. Experience using hand tools, measurement tools, and other manufacturing assembly aids. Mechanical aptitude and ability to troubleshoot electrical and mechanical equipment or fixtures. Ability to understand and adhere to standard operating procedures (SOPs) and work instructions. Ability to read & interpret manufacturing process instructions (MPI), quality inspection procedures (QIP), engineering specifications, or other engineering/manufacturing documentation. Must be able to lift objects up to 50 lbs. PREFERRED QUALIFICATIONS Experience working in a cleanroom environment. Catheter manufacturing experience (coil winding, lamination, coating). Knowledge of Quality System standards & regulations. Strong understanding of basic statistics. 3D CAD experience (On Shape or SolidWorks preferred). Fixture design, fabrication, and assembly. COMPENSATION: Our job titles may span more than one career level. The starting base pay for this role is between $35-$45 per hour. The actual base pay is dependent upon many factors, such as training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits, and 401(k) with matching. Jupiter Endovascular provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

We are seeking a skilled and diligent Senior Optics Assembly & Test Technician to join our client's team. The Optics Assembly and Test Technician is a specialized professional responsible for the meticulous assembly, alignment, and testing of precision optical components, cemented doublet/triplet, and opto-mechanical assemblies. The ideal candidate will possess excellent hand-eye coordination for working with small and delicate parts, such as lenses, mirrors, and windows, and have a strong background in optics and test equipment. This position is only available to US Citizens or US Permanent Residents Duties Perform precise assembly of optical and opto-mechanical components using fixtures, hand tools, and test equipment. Align and install various optical elements, such as lenses, mirrors, and windows, while monitoring optical parameters to meet specifications. Operate and maintain a variety of optical test equipment, including interferometers, profilers, and centration testing. Execute detailed test procedures to verify the performance and functionality of assembled products. Troubleshoot and repair complex opto-mechanical assemblies that fail during testing. Thoroughly clean and inspect optical components under a microscope for defects or contamination. Read and interpret detailed work instructions, engineering blueprints, and schematic diagrams. Maintain accurate records of all production, test data, and documentation. Adhere to all safety protocols and maintain a clean and organized work area, which may include a cleanroom environment. Collaborate with engineering teams to provide feedback on manufacturability and assist with the development of new processes. Requirements Education: High school diploma or GED required. An Associate's degree or certificate in a related technical field (e.g., Optics, Photonics, or Electronics) is preferred. Experience: A minimum of 5 years of hands-on experience in a manufacturing or lab environment with optical, fiber optic, or semiconductor systems. Technical Skills: Excellent manual dexterity and hand-eye coordination for working with small, delicate components. Proficiency with precision hand tools and optical metrology equipment. Basic understanding of optical principles, physics, mechanics, and electronics. Strong computer skills for operating test equipment and documentation.

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description Duties: Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Essential Technician: Operate systems that clean and sterilize tanks and filtration systems. Prepare solutions for the production process. Review documentation and check all calculations (e.g. tickets, labels, equipment reading). Trouble shoot equipment and process problems. Comply with safety requirements, cGMP, SOP and manufacturing documentation. Use of automation to perform production operations. Provide support to Manufacturing to meet production demands. Operate automated systems for equipment operation. Assemble and prepare equipment for production. Exhibit detail oriented documentation skills Communicate effectively and ability to work in a team environment. Exhibit professional interpersonal skills. Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues. Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Job Matrix A good working knowledge of biopharm technology and processes. Trained and skilled in all operational procedures of at least one manufacturing department. Demonstrated ability to independently document and record information related to the process. Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems. Recognizes non-routine problems, investigates and suggests potential solutions. Judgment is required in resolving problems and making routine recommendations. Ability to recognize deviation from accepted practices is required. Supplementary Responsibilities: Operate bioreactors, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up) Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Qualifications Degree in Life Sciences or engineering and 1 year related experience Or Associate Degree and 3 year experience Or High school and 5 years' experience Biotech certificate from approved program Additional Information Sneha Shrivastava Sr Technical Recruiter 862 - 579 - 4236

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: Purifies proteins in a regulated FDA licensed and ISO certified facility and performs cross-functional activities associated with downstream production runs in collaboration with Bulk Fill and QC testing groups. The role may include special projects such as process development and validation activities where scientific research principles are applied. Primary responsibilities: Purify recombinant proteins to ensure commercial product demands are met: 1. Works as part of the purification team to perform purification, filtration, and centrifugation operations according to standard operating procedures. 2. Executes laboratory operations including dispensing of chemicals, volumetric and gravimetric measurements, making accurate dilutions, and preparing solutions. 3. Performs SAP duties that include cycle counting, reservations, issuing to process orders, and charging of expiring raw materials. 4. Performs equipment preventative maintenance tasks, column packing, and column testing procedures. 5. Ability to multi-task and become proficient at purifying 14 different proteins and make conjugates. 6. Responsible for ordering raw materials and components, as required. 7. Maintains a safe and well-organized work environment and complies with safety procedures. Follow regulatory requirements: 1. Adheres to valid manufacturing procedures, manufacturing operations, and current good manufacturing practices (cGMP) and ISO requirements. Documentation: 1. Responsible for the completion and review of batch records and logbooks, which requires legible, clear, and concise data entry. 2. Completes all training documentation within a pre-defined timeframe. Analytical Testing: 1. Analyzes in-process samples generated from purification activities. 2. Operates lab equipment such as pH meters, balances, centrifuges, spectrophotometers, HPLC systems, and densitometers. Skills:Must have an understanding of protein purification processes. • Experience following and writing instructions. • Very good verbal and written communication skills. • Computer knowledge required with experience using MS Word and Excel. • Able to document work accurately and has excellent organizational skills. • Experience with preparation of reagents following instructions. • Delivers quality products and services on time to all customers. • Must be attentive to detail. • Effectively manages time. • Considers how all daily manufacturing activities impact product quality. • Monitor processes and products to identify opportunities for continuous improvement. • Able to lift and push up to 35 lbs. 1. Works well in a team environment to manufacture production lots. 2. Complies with cGMP and ISO requirements. 3. Maintains accurate documentation related to manufacturing processes. Education:BA/BS in the sciences (Biology, Engineering, or related field) or 2 years of relevant experience Languages:English Read Write Speak Additional Information Best Regards, Anuj Mehta ************