Manufacturing associate jobs in Watsonville, CA

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.

As a Manufacturing Operator, you will play a critical role in the manufacturing process by assembling high-quality products in accordance with detailed specifications and standard operating procedures. You will ensure that each component is accurately integrated, contributing to the overall integrity and performance of our medical and diagnostic products. Your responsibilities will include maintaining optimal production efficiency by monitoring workflow, identifying bottlenecks, and implementing solutions to streamline operations. You will perform rigorous quality control tests, inspecting raw materials, subassemblies, and finished goods to uphold Roches commitment to excellence and compliance with regulatory standards. In addition, you will manage inventory levels to support uninterrupted production, operate tools and machinery with precision and safety, and promptly report any issues or deviations to supervisors to ensure continuous improvement and operational excellence. Job Description Duties: • Assemble products following specifications - Accurately assemble components according work instructions - Use appropriate tools and equipment to complete builds efficiently and precisely • Maintain production efficiency - Follow standardized procedures to ensure consistent output and product quality - Monitor workflow to meet daily and weekly production targets while minimizing downtime. • Perform quality control tests by inspecting raw materials, subassemblies and finished products to ensure product integrity. • Inventory management • Operate tools and machinery safely • Report issues to supervisors Who You Are • 5 years + in the manufacturing environment • Strong problem-solving skills • Excellent communication abilities • Proficiency in industry tools/software • High School Diploma / GED required • Ability to have prompt, regular and reliable work attendance required Physical Requirements: Must be able to lift 25 pounds Standing for 8 hours per day Fully On-Site role in Santa Clara, CA. Monday-Friday 7am-3:30pm Education Requirements: High School Diploma/GED Years of Experience Required: 5 years

Medical Device Manufacturing Operators Pay $25.00 - $30.00 6 month+ assignment Onsite in Campbell, CA EDUCATION/EXPERIENCE: • A minimum of 4 years related experience in the medical device industry; or equivalent combination of education and work experience. • Must be certified on all processes of work area, including certified as expert on all critical processes. • Training, skill, or experience from a trade is preferred. • Highly skilled in product manufacturing, testing, and data collection. • Proficient with GMP, GDP procedures and requirements as they relate to production lines. • Strong ability to be reliable, work independently or in team setting and take initiative. • Strong ability to coach and train others on manufacturing processes and procedures. • High skill on operating manufacturing equipment (i.e. hot boxes, adhesives, soldering, bonding, fuse joining). • Proficient with testing: tensile, simulated use testing, or tests related to assigned projects. • Expert hand dexterity and ability to work with small components. • Strong written and verbal communication skills. • Strong computer skills, including knowledge of Microsoft office products. • Strong interpersonal skills, effective interaction with Operations and other departments ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: • Operate with high skill, manufacturing and packaging equipment following Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP). • Uses high level of expertise to work with in-house and contract manufacturers and ensure products are manufactured adhering to product plans, quality, and regulatory requirements. • Collaborate with manufacturing and engineering personnel to understand product requirements, identify and implement process improvements. • Perform complex troubleshooting and maintain workspace and equipment clean. • Adhere to strict safety regulations of the company; maintain a safe, clean and organized work area, and ensure that others are doing the same. • Perform manufacturing processes using Manufacturing Process Instructions (MPI's), while assisting in the development of new processes or test procedures through feedback. • Record and review accuracy of data on lot history records (LHR's) in collaboration with manufacturing, quality, and R&D. • Meet regular attendance and punctuality expectations and adhere to all company policies. • Learn and adhere to safety requirements of manufacturing processes, equipment, handling of chemicals and materials, and apply high skills during complex operations. • Accurately use computerized operating systems to run and monitor manufacturing equipment. • May oversee the set up and operation of a variety of equipment to produce materials and assemblies. • Monitor and record critical process parameters and ensure that proper documentation and GDP guidelines are followed by others. • Contribute to manufacturing team meetings to ensure communication between members. • Help build engineering prototypes and products used in preclinical/clinical evaluations. • Must be a Certified Trainer and teach/train others on manufacturing processes. • Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy. • Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, applicable FDA, and Regulatory requirements. Benefits (employee contribution): Health insurance Health savings account Dental insurance Vision insurance Flexible spending accounts Life insurance Retirement plan All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

At Western Digital, our vision is to power global innovation and push the boundaries of technology to make what you thought was once impossible, possible. At our core, Western Digital is a company of problem solvers. People achieve extraordinary things given the right technology. For decades, we've been doing just that-our technology helped people put a man on the moon and capture the first-ever picture of a black hole. We offer an expansive portfolio of technologies, HDDs, and platforms for business, creative professionals, and consumers alike under our Western Digital , WD , WD_BLACK™, and SanDisk Professional brands. We are a key partner to some of the largest and highest-growth organizations in the world. From enabling systems to make cities safer and more connected, to powering the data centers behind many of the world's biggest companies and hyperscale cloud providers, to meeting the massive and ever-growing data storage needs of the AI era, Western Digital is fueling a brighter, smarter future. Today's exceptional challenges require your unique skills. Together, we can build the future of data storage. Job Description ESSENTIAL DUTIES AND RESPONSIBLITIES: Disposition hold wafer according to SPEC or disposition criteria provided by PE. Disposition hold wafer with own judgement based on risk assessment/process expertise/related previous experience. Troubleshoot the failure and differentiate if defect is incoming or from current oper. Detailed knowledge of process recipe for each tool set. Capable of identifying point of failure if process recipe related. Collect, analyze and send data to PE/EE/MFG when needed and recommend solution In-depth knowledge of IT-related application/software such as MITECS, GS3, TSD, TDM, Flexicton, Spotfire report, EDCSPC, SPC chart, CAMSTAR, Dashboard, Fabtime, etc. Work with PE, EE and Maint tech in troubleshooting tool failure. Provide input from manufacturing/process point of view. Notify PE/MFG if there's any suspected excursion. Do preliminary investigation and identify/hold all potentially affected wafers to contain the problem and minimize the impact. Quality agent in the line Knowledge of Vacuum processes tools functionality as well as knowledge on associated metrology tools Descent analytical skills to analyze the problem & translate the issue to appropriate supporting engr. Qualifications REQUIRED: 3+ years of experience in running TF process tools & related metrology tools. SKILLS: Able to communicate and have a good command of the English language. Proficient in basic computer applications. Must demonstrate the ability to effectively and efficiently work among. multidisciplinary teams and mfg. technicians. Experience in TF department Good written and verbal communication skills Descent analytical skills to analyze the problem & translate the issue to appropriate supporting team Additional Information Western Digital is committed to providing equal opportunities to all applicants and employees and will not discriminate against any applicant or employee based on their race, color, ancestry, religion (including religious dress and grooming standards), sex (including pregnancy, childbirth or related medical conditions, breastfeeding or related medical conditions), gender (including a person's gender identity, gender expression, and gender-related appearance and behavior, whether or not stereotypically associated with the person's assigned sex at birth), age, national origin, sexual orientation, medical condition, marital status (including domestic partnership status), physical disability, mental disability, medical condition, genetic information, protected medical and family care leave, Civil Air Patrol status, military and veteran status, or other legally protected characteristics. We also prohibit harassment of any individual on any of the characteristics listed above. Our non-discrimination policy applies to all aspects of employment. We comply with the laws and regulations set forth in the "Know Your Rights: Workplace Discrimination is Illegal” poster. Our pay transparency policy is available here. Western Digital thrives on the power and potential of diversity. As a global company, we believe the most effective way to embrace the diversity of our customers and communities is to mirror it from within. We believe the fusion of various perspectives results in the best outcomes for our employees, our company, our customers, and the world around us. We are committed to an inclusive environment where every individual can thrive through a sense of belonging, respect and contribution. Western Digital is committed to offering opportunities to applicants with disabilities and ensuring all candidates can successfully navigate our careers website and our hiring process. Please contact us at [email protected] to advise us of your accommodation request. In your email, please include a description of the specific accommodation you are requesting as well as the job title and requisition number of the position for which you are applying. Based on our experience, we anticipate that the application deadline will be 11-15-2025 (3 months from posting), although we reserve the right to close the application process sooner if we hire an applicant for this position before the application deadline. If we are not able to hire someone from this role before the application deadline, we will update #LI-BL1 Compensation & Benefits Details An employee's pay position within the salary range may be based on several factors including but not limited to (1) relevant education; qualifications; certifications; and experience; (2) skills, ability, knowledge of the job; (3) performance, contribution and results; (4) geographic location; (5) shift; (6) internal and external equity; and (7) business and organizational needs. The salary range is what we believe to be the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range and this range is only applicable for jobs to be performed in California, Colorado, New York or remote jobs that can be performed in California, Colorado and New York. This range may be modified in the future. If your position is non-exempt, you are eligible for overtime pay pursuant to company policy and applicable laws. You may also be eligible for shift differential pay, depending on the shift to which you are assigned. You will be eligible to be considered for bonuses under either Western Digital's Short Term Incentive Plan (“STI Plan”) or the Sales Incentive Plan (“SIP”) which provides incentive awards based on Company and individual performance, depending on your role and your performance. You may be eligible to participate in our annual Long-Term Incentive (LTI) program, which consists of restricted stock units (RSUs) or cash equivalents, pursuant to the terms of the LTI plan. Please note that not all roles are eligible to participate in the LTI program, and not all roles are eligible for equity under the LTI plan. RSU awards are also available to eligible new hires, subject to Western Digital's Standard Terms and Conditions for Restricted Stock Unit Awards. We offer a comprehensive package of benefits including paid vacation time; paid sick leave; medical/dental/vision insurance; life, accident and disability insurance; tax-advantaged flexible spending and health savings accounts; employee assistance program; other voluntary benefit programs such as supplemental life and AD&D, legal plan, pet insurance, critical illness, accident and hospital indemnity; tuition reimbursement; transit; the Applause Program; employee stock purchase plan; and the Western Digital Savings 401(k) Plan. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Notice To Candidates: Please be aware that Western Digital and its subsidiaries will never request payment as a condition for applying for a position or receiving an offer of employment. Should you encounter any such requests, please report it immediately to Western Digital Ethics Helpline or email [email protected].

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values * Start with Authenticity: We foster an inclusive environment where each person can bring their authentic self to w * Think 'we' before 'me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. * Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Manufacturing Associate II, your mission is to deliver to patients every time! Our potentially life-saving treatments would not exist without the work of our manufacturing team. Your work will have a tremendous impact on our ability to deliver our transformative cell therapy to the patients who need it most. The "Fine Print" - What You'll Do * Key Responsibilities * Accurately follow manufacturing batch records (MBRs) and standard operating procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) * Execute end-to-end cell therapy manufacturing operations including: * Operation of manufacturing equipment for batch production * Media preparation, reagent handling, buffer preparation * Aseptic processing in controlled cleanroom environments * Document all activities in accordance with Good Documentation Practices (GDPs) * Support deviation investigations, CAPA execution, and change control activities * Complete all training activities required to maintain quality compliance. * Maintain strict compliance with regulatory and internal quality standards * Perform routine maintenance activities required for a GMP environment Skills and Experience We Look For * Bachelor's degree in relevant scientific field and 2+ years of industry experience in manufacturing (cell therapy, biologics, or aseptic manufacturing environment) * Familiarity with mammalian cell culture and aseptic techniques * Ability to operate within a clean room environment for long duration * Understanding of GMP principles and cleanroom operations * Excellent organizational and prioritization skills * Exceptional collaboration, communication, and interpersonal skills * Flexibility to work weekends, holidays, or shift schedules as required Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $80,000 - $120,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

Figure is an AI Robotics company producing a general purpose humanoid. Our Humanoid is designed for corporate or in-home tasks targeting labor shortages and jobs that are undesirable or unsafe. We are based in San Jose, CA and require 5 days/week in-office collaboration. We are looking for a Manufacturing Repair Technician to compliment our superstar team building and improving the product of the future. Responsibilities: Repairing full robots and smaller sub-assemblies for F.03 high volume manufacturing Diagnosing electrical, mechanical, and software issues. Document issues found, steps taken, and root cause of all repairs. Validating and improving repair procedures for repeat issues and future remanufacturing of failed in field robots and sub-assemblies Supporting any immediate need to keep manufacturing moving at a high rate Requirements: 3+ years experience working with complex systems Familiarity with computer based tools such as but not limited to Google Suite, Confluence, Jira, and an interest to learn command prompt and product specific software Comfortable using a Digital Multi Meter Familiarity with torque tools and mechanical assembly Ability to follow assembly documentation Ability to build with little to no documentation with engineering support Complex system diagnostic ability Great attitude and excited to face challenges Bonus Qualifications: Manufacturing experience Computer based design experience Automotive experience Fabrication experience Soldering experience Small brushless motor experience Robotics experience

Are you a current Elekta employee? Please click here to apply through our internal career site Find Jobs - Elekta. Want to join a team with a mission to improve and save lives? We continually look for motivated and skilled individuals who are interested in supporting our customers - healthcare professionals who use our products to help patients and their communities. We currently have the following opportunity available - please contact us for more details! We don't just build technology. We build hope for everyone dealing with cancer. This is an on-site job at the San Jose, CA office 5 days a week The Manufacturing Technician (Xoft) performs a range of medical device assembly and processing tasks as part of the production team. Responsibilities: · Assemble, inspect, test, package, and label medical devices per documented procedures. · Complete production documentation accurately and follow quality management and safety standards. · Execute tasks based on production orders, drawings, and work instructions, consulting the manager on progress and priorities. · Perform final testing, record data in measurement reports, and assign lot/serial numbers to products. · Participate in the manufacturing team's processes and contribute to facility safety as a member of the Xoft safety team. · Transact Manufacturing Orders using the ERP system. · Manage inventory accurately, in assigned work space · Participate in Inventory Counting in preparation for Audits · Represent process steps where trained, during Quality System Audits. · Document accurate work instructions for all processes and collaborate with the manager to design and produce assembly tools. · Support other production teams as needed. · Adhere to regulations regarding Medical Device Manufacturing (FDA 510, ISO 13485, MDR). · Follow Lean Manufacturing principles, including waste reduction and 5S practices. · Take initiative in proposing and implementing improvements, actively contributing to projects. · Technical background equivalent to Grade 12. Qualifications- · Experience and/or a desire to learn high-skill medical device cable assembly. · Ability to assemble micro-scale devices under a microscope for extended periods. · Proficiency in using measurement equipment and maintaining accurate process records. · Knowledge or experience in medical product treatment standards (e.g., FDA 510k, ISO 13485 guidelines). · Familiarity with GMP (Good Manufacturing Practices) is advantageous. · Resourceful in ordering parts, working with vendors, and daily problem-solving. · Ability to maintain detailed records following good documentation practices. Skills: · Basic computer knowledge and skills. · Fluent in English (written and oral). · A continuous desire to learn new processes and skills. · Effective communication skills: sharing information, knowledge, openly and honestly. Actively listening and clarifying messages. Demonstrating consistency between words and actions. · Initiative: Recognizing opportunities and taking proactive steps. Competencies: · Commitment and involvement: proactive, results-oriented, enthusiastic, self-driven. · Committed to quality: efficient, sets high standards, focused on improvement. · Adaptability to changes: flexible and open to new ideas. · Demonstrates creativity: innovative and visionary thinking. · Positive influence: confident, assertive, and persuasive, creating a positive impression. · Takes responsibility for personal development: self-aware, motivated, and curious. · Expert knowledge: skilled, professional, up-to-date. · Effective teamwork: supportive, encouraging, cooperative · Work may occur in a Cleanroom, following Gowning Protocols What you'll get: In this role, you will work for a higher purpose; hope for everyone dealing with cancer, and for everyone regardless of where in the world, to have access to the best cancer care. In addition to this, Elekta offers a range of benefits. What we offer: Excellent Medical, Dental and Vision coverage 401k, paid vacation and holiday A wealth of additional benefits including wellness reimbursement, tuition reimbursement and flexible spending account Close-knit company culture Career development - wide range of learning opportunities How to proceed? We are looking forward to hearing from you! Apply by submitting your application and résumé in English, via the “Apply” button. Please note that we do not accept applications by e-mail. We are an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, disability, veteran status, or any other protected characteristic. The US base salary range for this position is $32-35/hr. About Elekta As a leader in precision radiation therapy, Elekta is committed to ensuring every patient has access to the best cancer care possible. Elekta is a proud innovator and supplier of equipment and software used to improve, prolong, and save the lives of people with cancer and brain disorders. More than 6,000 hospitals worldwide rely on Elekta technology. We openly collaborate with customers to advance sustainable, outcome-driven, and cost-efficient solutions to meet evolving patient needs, improve lives and bring hope to everyone dealing with cancer. To us, it's personal, and our global team of 4,700 employees combine passion, science, and imagination to profoundly change cancer care. We don't just build technology, we build hope. Elekta is headquartered in Stockholm, Sweden, with presence in more than 120 countries and listed on Nasdaq Stockholm. For more information, visit elekta.com or follow @Elekta on Twitter and on LinkedIn.

Job DescriptionSalary: $26 - $33 Pivotal Systems provides the best-in-class gas flow monitoring and control technology platform for the global semiconductor industry. The companys proprietary hardware and software utilizes advanced machine learning to enable preventative diagnostic capability resulting in an order of magnitude increase in fab productivity and capital efficiency for existing and future technology nodes. Job Overview: A Manufacturing Technician is precision and quality oriented with the ability to work efficiently. The primary role is to build new products in the Manufacturing cleanroom. Which also includes quality inspection of materials, testing, basic troubleshooting, and communication of issues/improvement. Comfortable with use of tools and Software interfaces. Ensure all stations performances are up to par. Essential Duties And Responsibilities A Manufacturing Technician performs process tasks from kitting to finished goods. Use manufacturing software application to track in and out of each process. Perform failure analysis and repair of failed units. The MT understands and follows assembly instructions, drawings, and work orders; is not hesitant to ask questions for clarification. Expectations are for the MT to learn and apply advanced assembly procedures, to include detailed hardware installation, in-process, and final assembly of a wide variety of parts and models. Able to understand basic principles of gas flow, units of pressure, voltage, resistance, and torque. Must be able to write clearly on product/unit traveler and in application comment section to communicate with others. Must work well under pressure with many products in various states of assembly and multiple deadlines. The MT shall always demonstrate cooperative behavior with colleagues and supervisors. Able to understand and comply with Safety Practices and ISO 9001:2015 Class 6-7 Clean-room Practices. Identifies and obtains equipment, tools and materials needed to properly perform job function. Knowledge of common hand tools, torque wrenches and demonstrated mechanical capabilities. Being at work on time and maintaining good attendance is a condition of employment and is an essential function of the job. Use and knowledge of epoxy resins and proper handling. Able to use cleanroom packaging materials and equipment for shipments. Able to train and mentor new technicians or others. Willing to share proper procedures and guidelines applicable to company mandates. Additional Duties Support R&D/Engineering as requested Supervisory Responsibilities Must be willing to maintain daily, weekly, monthly, and quarterly equipment worksheets, signing off on operability, and maintained in good order. Education And/Or Experience High school diploma or GED required AA degree and/or College or Trade School Preferred. 3+ years experience in related field may be substituted for education. Must be willing to pass annual Cleanroom Technician quizzes and tests in accordance with ISO 9001:2015 Standards. Language, Mathematical, And/or Reasoning Ability English (fluent) written and spoken. Must be comfortable with writing detailed notes and asking for assistance when clarifying information. Must be able to follow verbal and written, detailed directions, meet deadlines, and operate as a team member. Must be able to receive and execute safety and Copy Exactly training. Must pass all Pivotal training requirements and certifications prior to working alone on a station. Physical Demands Pick up and lift to 50lbs, no allergies to latex, no asthma. Must be able to detect colors. Demonstrates careful use of glues, epoxies and solvents. Work Environment Must be able to perform repetitive tasks for an entire shift. Over time when needed. Must be able to sit, stand, or crouch down for extended periods. Use of hairnets, latex gloves, shoe coverings, and lab gowning is always required. Must be willing to keep workstations neat and tidy, placing tools into workstation designated areas. Perform occasional tasks of keeping cleanroom and gowning room areas clean. Emptying trash, and refill fluids to chiller/HX as needed.

We look for a motivated Associate Manufacturing technician who can perform a wide variety of product assembly operations on product components, assemblies or sub-assemblies to make essential laboratory equipment. You will work safely and ensure best quality products within specified times. You will engage with your colleagues to troubleshoot problems and drive continuous improvement in the factory. What will you do? •Select appropriate components to align and assemble them in proper sequence to meet specifications. •Inspect parts during sub-assembly and at key points to ensure the unit meets specified quality standards prior to moving unit to the next workstation. •Use a wide range of hand tools, including, but not limited to drill, pneumatic press, and/or torque wrenches. •Utilize our internal system to enters product-related data into computer system to track component serial numbers, scan bar codes, production rates, track physical location, etc. •Troubleshoots work-related problems by applying knowledge and experience toward resolution and taking appropriate steps for assistance. •Test assembled units, clean and pack final product. •Ability to read, understand, document accurately, and communicate clearly in English is required. Demonstrate proficiency to learn and perform simple to more complex basic math operations, understanding / application of decimal and scientific notation and basic chemistry concepts. •Demonstrate proficiency in the setup and use of basic laboratory equipment. •Ability to learn and demonstrate proficiency in performing simple to more complex bench-top and chemistry analyzer testing. Able to wear personal protective equipment such as safety glasses, hard-toe shoes, laboratory coat, gloves, chemical resistant suits. Air purifying respirator, and dust mask for long periods might be needed for specific task. Interaction with Other Employees (level of contact, purpose and frequency) •Regularly communicate with the Lead and Supervisor to take the daily assignment and to report any relevant production related information during the day. •Works frequently with Manufacturing Engineers to improve Quality/Quantity of products Knowledge, Skills, Abilities •Ability to read and differentiate part numbers, labels, and work instructions. •Standing, bending, reaching, and handling small parts is common to the job. Occasionally lifts up to 35 pounds. •Computer and keyboarding. Physical/Environmental requirements: •Constant Physical requirements: Siting, Stooping, kneeling, crouching, reaching, standing, walking, twisting, pushing, pulling, lifting, fingering, grasping, feeling, talking, hearing, pinching, neck rotations, repetitive motions, and keyboarding. Visual inspection involving small defects, small parts, operation of machines, using measurement devices, assembly, and fabrication of parts at distances close to the eye. 20 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Occasionally Physical Requirements: Climbing, squatting, and crawling. Exerting up to 50 pounds of force. •Environmental Conditions: The worker is subject to hazards: Including a variety of physical conditions, such as proximity to moving mechanical parts, electrical current, exposure to high heat and exposure to chemicals. 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.

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Secure the Future: Join Teledyne as a Manufacturing Technician-$5K Sign-On Bonus!** **Build technology that powers critical missions.** At Teledyne Microwave Solutions, we've spent over 50 years designing and manufacturing advanced RF and microwave components for aerospace, defense, and communications. Our products support applications from radar and space to electronic warfare and UAV systems. If you're ready to bring your technical expertise to a team that values precision and innovation, join us as a Manufacturing Technician on our Day Shift. **What you'll do** + Perform chem-film (alodyne) processes on metal surfaces + Apply conformal coating on PCBs and conduct solvent tests + Analyze test results and troubleshoot process issues + Work with chemicals, cleaning agents, microscopes, and precision tools + Review work instructions and drawings to ensure compliance with specifications + Set up and conduct tests on components and assemblies under operational conditions + Record test procedures, results, and recommend improvements + Support continuous improvement initiatives and maintain quality standards **What you need** + Strong attention to detail and ability to follow technical procedures (required) + Experience with chem-film and conformal coating processes (required) + Ability to use diagnostic equipment such as oscilloscopes and spectrum analyzers (required) + Knowledge of ISO and/or AS9100 standards (required) + Working knowledge of Lean Manufacturing/6 Sigma principles (advantage) + Vocational or technical certificate and 5-10 years of related experience (required) + U.S. citizenship and ability to obtain security clearance (required) **What we offer** + **$5,000 sign-on bonus** + Competitive salary and comprehensive health benefits + 401(k) with company match and retirement plans + Paid time off and flexible work arrangements + Professional development and training opportunities + A collaborative environment focused on innovation and growth **What happens next** Apply online through Teledyne's careers page. If your qualifications align, our team will contact you for interviews and guide you through the next steps. _Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status._ **Salary Range:** $42,800.00-$57,100.000 **Pay Transparency** The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

Position Title: Manufacturing Technician II / Catheter Assembly Technician Job Location: 4245 Technology Drive, Fremont, CA 94538 Department: Operations Mfg Techs Worker Category: Full-Time/Hourly Job Class: Assembly Technician 2 FLSA: Non-Exempt Job Industry: Neurovascular Medical Devices (Catheters) Function: Assembly Technician Schedule: Monday - Friday Shift: 8:00 AM - 4:30 PM Who We Want: Q'Apel is seeking a Manufacturing Technician II / Catheter Assembler to support and maintain efficient, timely, and effective production operations. A minimum of 2-3 years of manual catheter assembly experience in the Neurovascular Devices Industry, Neurointerventional, Endovascular Neurosurgery, Neuro-interventional, Coronary or Peripheral Medical Device sectors is required to be considered. The ideal candidate will have recent hands-on experience assembling neurovascular catheters, demonstrating excellent manual dexterity, visual acuity, strong attention to detail, and the ability to follow strict instructions. The assembly process must be followed exactly from the written Standard Operating Procedures (SOP's) to meet safety and high-quality standards. We're looking for someone who has proven and proficient microscope skills capable of performing detailed assembly and inspection tasks for extended periods (up to 8 hours per day). Can safely and effectively operate manual cutting tools and other assembly equipment. Follows work instructions accurately and consistently to ensure high product quality and deliver on output. The ideal assembly technician must be comfortable working in a dynamic environment with rapidly changing priorities and demonstrate flexibility to quickly adjust to new tasks and assignments as needed. At Q'Apel, every team member “steps up to the plate.” We are a fast-paced, high-growth company with a startup mindset. We value collaboration, adaptability, and a positive attitude toward change. If you thrive in a dynamic environment and take pride in precision work, we'd love to have you on our team. About Q'Apel: At Q'Apel, we are passionate about revolutionizing neurovascular access. In the simplest sense, we're a company that creates solutions. We design novel access device technology for vascular interventions and unmet clinical needs. Because in the precious seconds that surround a stroke emergency, clinicians need technology that delivers. That's where Q'Apel comes in. Successful Q'Apel team members step up to the plate and work together to achieve our goals every single day. We are a fast-paced, high-growth company with a startup philosophy that requires an all-hands-on-deck attitude, taking on all changes with excitement and a great attitude. What You'll Work On: Daily accurate manual assembly of the neurovascular catheter per SOP guidelines. Supports production needs as scheduled and remains flexible. Performs manufacturing inspection and testing of catheter products to ensure they meet specifications. Accurate documentation and consistent records maintenance. Working daily in the controlled environment room (CER). Accurately and consistently follow FDA Quality Systems Regulations and ISO 13485 Assists Manufacturing with production issues and improvements. Assists in investigations and testing for new or revised production procedures. Adheres to approved standard operating procedures and manufacturing procedures. Unlimited/continuous use of a microscope. Unlimited/continuous use of manual cutters. Opening, lifting, and packaging shipper boxes approximately 10 lbs. in weight on a continuous basis. Provide consistent daily product output. Ability to stay flexible and transition from one station to another, one task to another. Daily communication and ability to clearly explain any assembly-related problems. Other duties as requested. What You Bring: Education: High School degree required Experience & Skills required: Minimum 2-3 years of recent catheter assembly experience required. Good manual dexterity and visual acuity required. Effective communication skills (both written and verbal) required. Ability to work independently or in a team setting. Ability to lift up to 10 lbs Is organized and self-motivated Minimum 2-3 years of experience working in a regulated industry (medical device development experience, along with a solid working knowledge of FDA Quality System Regulations and ISO 13485) Minimum 2-3 years of experience working in a controlled environment room (CER) required Knowledge and exposure to applicable regulations (QSR, MDD, CMDR, and ISO) required Our hourly compensation ranges are calculated by role and level. Your position within that range will be determined by your job-related knowledge, skills, experience, relevant education, and training/certifications. In addition to those factors, we also examine internal equity as well as consider the current market rate, and the title may be assessed one level lower or higher accordingly. After you join the company your performance, contributions, and results along with business and organizational needs will affect your hourly compensation. The hourly compensation range for this full-time, non-exempt position is between $25.00/hour to $28.00/hour + equity + benefits.

Join our team of battery innovators in a dynamic, supportive start-up environment to enable the next generation of hearables, wearables, and IoT-connected sensors with Ensurge's groundbreaking solid-state microbatteries. Ensurge solid-state microbatteries offer multiple times the energy density and charge cycles of lithium-ion alternatives. We enable a wide range of battery shapes and sizes, unleashing designers' creativity and enabling previously impossible applications. We are looking for a Manufacturing Technician to work at our state-of-the-art flexible electronics manufacturing facility located in the heart of Silicon Valley. In this position, you will operate the process equipment for our sheet and roll-to-roll production line. This position will work on our swing shift. This position will work on our AWS (Mornings from 6 am to 6 pm, Sunday to Tuesday, every other Wednesday). The successful candidate will be a hands-on, detail-oriented team player. The role requires frequent bending, lifting, and eye-hand dexterity, as well as the physical movement of products and storage containers weighing up to 25 pounds. This is an exciting opportunity for a self-motivated individual with the drive to take initiative in a fast-paced environment and experience SSLB innovation, with prospects for career growth within the company. Responsibilities * Operate the process equipment in the sheet and roll-to-roll manufacturing line * Carry out assignments with limited supervision and enter data accurately into the process control system * Make visual judgments on product quality, including subtle differences in coloring and shading * Record production, downtime, inventory, and quality transactions as required * Work in a cleanroom environment wearing appropriate cleanroom garments and follow cleanroom policies and practices * Maintain a safe, clean, and organized work environment * Work on other assignments or related projects as needed, including with maintenance and/or process teams Requirements * At least seven years of experience operating semiconductor manufacturing process equipment * Good working knowledge of a variety of semiconductor processes and best practices for running recipes/equipment * Ability to learn and operate complex equipment * Ability to cope with change in a dynamic team environment * Must be able to work overtime as needed. * Role requires frequent bending, lifting, eye-hand dexterity, and the physical moving of product and storage containers up to 15 pounds * Discipline to adhere to safety and change control measures * Must have good written and verbal communication skills * High school diploma or equivalent

We are looking for a driven individual who thrives in a fast-paced dynamic work environment, being hands on and interacting with innovative, new and exciting tech. We can offer the opportunity to grow Electromechanical skills plus long term career growth opportunities. The Manufacturing Technician I will work on site 5 days a week in Santa Clara, CA. This person is primarily responsible for providing updates to the line lead/ engineers of build/work status. In addition, identifies problems with recommendations for improvement or correction. They will assist in modifying procedures to improve equipment operation or processes. They record assignments and prepare documentation concerning materials, parts used, concepts, designs, drawings, and processes. This role reports into the Surgical Robotics Manufacturing organization. Do you use your technical and interpersonal communication skills to work in group settings and seek out diverse perspectives with multi-functional team members? Join our team to take part in this unique and exciting new product introduction! We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Must-haves - 3+ years of experience as an assembler, tester, or associate of a Type I, II or III medical device company or complex electromechanical capital equipment manufacturer - Electrical troubleshooting experience such as proper use of Loctite, Torque Wrenches, multimeter, isolation, grounding, use oscilloscope to aid problem solving. - Understanding of Good Documentation Practices (GDP) - Proficient at multiple assembly and test tasks while meeting requirements for workmanship, safety, and productivity - Relevant demonstrated experience with anti-static/ESD principles and controls. - Vocational training Certificate, Technical or associate's degree - Experience with using Learning Management Systems such as cornerstone, AGILE PLM, MES, ERP experience (SAP, QAD, Camstar) - Electrical troubleshooting experience such as proper use of Loctite, multimeter, isolation, grounding, use oscilloscope to aid problem solving.

Rapidly Growing Life Sciences Technology Company Ultima Genomics is a rapidly growing company that is developing ground-breaking genomics technologies. Our mission is to continuously drive the scale of genomic information to enable unprecedented advances in biology and improvements in human health. We have developed a foundational new approach to sequencing at scale that overcomes limitations due to the high costs of current technologies. We are well-funded and have raised approximately $600 million from global top-tier investors. Our team brings together unique and diverse expertise across multiple disciplines, from healthcare and life sciences, to engineering, to technology and software and beyond. We are a collaborative group, including successful entrepreneurs, chemists, hardware and software engineers, genomics and biotechnology experts, molecular and computational biologists, software and algorithm experts, and operations and commercial leaders. Join us to develop and commercialize technologies that unleash the power of genomics at scale and empower the future of human health. We are looking for a highly motivated Manufacturing Technician to join our team! This opportunity is an onsite full-time Monday-Friday contracting position based in our Fremont, CA office. How You'll Contribute Follow lab protocols and procedures Assemble, kit, package, label consumables Maintain accurate and thorough batch records Manage shared laboratory equipment, perform required instrument calibrations as needed and support instrument maintenance Prepare, characterize, and perform quality control assays on reagents and buffers Monitor, track and maintain inventory of raw materials and lab consumables Other job duties as assigned Qualifications, Skills, Knowledge & Abilities AA/AS in chemistry, biochemistry, biology, or closely related field OR relevant reagent or consumable manufacturing experience Experience working in a laboratory environment a plus Some basic wet lab skills - weighing, measuring, pH, mixing, using balances, micropipettes, serological pipettes Meticulous and detail-oriented, ability to follow work instructions with reproducible results and thorough documentation of work Excellent organizational, communication and time management skills Motivated and willing to work in a fast-paced environment as part of a hard-working and multidisciplinary team #LI-Onsite Ultima Genomics is proud to be an equal opportunity workplace and is an affirmative action employer. We provide equal employment opportunity for all applicants and employees. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), gender identity, gender expression, national origin, ancestry, citizenship, age, physical or mental disability, military or veteran status, marital status, domestic partner status, sexual orientation, genetic information, or any other basis protected by applicable laws. See also Ultima Genomics' EEO Policy and Know Your Rights. If you have a disability or special need that requires accommodation, please let us know by contacting ************************.

Job DescriptionBenefits: 401(k) Health insurance Paid time off Vision insurance Job Title: Pharmaceutical Manufacturing Technician I Reports to: Manufacturing Manager Summary: Responsible for the manufacturing of pharmaceutical products in a GMP environment. Duties and Responsibilities include the following. Other duties may be assigned. Perform daily manufacturing tasks as assigned by supervisor. Weigh materials, prepare solutions and production materials. Perform manufacturing packaging and related tasks. Document production activities in manufacturing batch records. Clean up production equipment and production area. Clean and prepare manufacturing equipment Clean and maintain production areas Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education/Experience: Minimum High School Diploma or GED and three (3) to five (5) years related experience in a GMP pharmaceutical manufacturing environment. Experience with analytical balances, weighing materials accurately. Experience with handling of solids and liquids, pouring and filtering. Language and Communications Ability: Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form. Ability to read, understand and legibly enter data in production batch records. Ability to read and understand equipment manuals. Math Ability: Ability to use a calculator to add, subtract, multiply, and divide different units of measure, using whole numbers, common fractions, and decimals. Reasoning Ability: Ability to recognize and communicate practical problems in the production environment. Ability to troubleshoot under supervision. Computer Skills: The individual should have a working knowledge of Microsoft Word and Microsoft Excel plus basic email and internet functions. Specialized Training: GMP Training in a pharmaceutical manufacturing environment. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals. Appropriate personal protective equipment is provided. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand, walk, sit, use hands or talk/hear. The employee is occasionally required to reach with hands and arms, climb or balance, and stoop, kneel, crouch or crawl. The employee must occasionally lift and/or move up to 75 pounds, as well as rolling equipment that is over 100 lbs. Location: Must be located in the Bay Area or willing to relocate at own expense Medterials is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Our client, a world leader in the semiconductor industry, is looking for a “Manufacturing Technician 5”. Job Title: Manufacturing Technician 5 Shift Hours: 8.00 AM to 5.00 PM or 9.00 AM to 6.00 PM Job Duration: Long-term Contract on W2 (Onsite) Location: Milpitas, CA Responsibilities: • This role is for a Contractor to do Server Assembly/Cabling/Trouble Shooting on Prototype and Shipper Racks • - Top 3 Daily Responsibilities • Build and Assemble Servers • T/S Server/Rack Power up issues • Logistics and Hardware RMA Management Additional Responsibilities • Create Interconnect Diagrams. • Create Documentation for Cabling • Train ATE's and Upgrade Engineers Required Skills: • Experience with Server/Rack Hardware. • Cable Management, Routing, and modification • 5+ Years for Experience • Good work ethic with through follow-through and closure. Company Benefits: Medical, Dental, Vision, Paid Sick leave, and 401K Interested! Please apply or send your resume to **********************.

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Rockville, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with Authenticity: We foster an inclusive environment where each person can bring their authentic self to w Think ‘we' before ‘me' : We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge : We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As a Manufacturing Associate II, your mission is to deliver to patients every time! Our potentially life-saving treatments would not exist without the work of our manufacturing team. Your work will have a tremendous impact on our ability to deliver our transformative cell therapy to the patients who need it most. The “Fine Print” - What You'll Do Key Responsibilities Accurately follow manufacturing batch records (MBRs) and standard operating procedures (SOPs) in accordance with current Good Manufacturing Practices (cGMPs) Execute end-to-end cell therapy manufacturing operations including: Operation of manufacturing equipment for batch production Media preparation, reagent handling, buffer preparation Aseptic processing in controlled cleanroom environments Document all activities in accordance with Good Documentation Practices (GDPs) Support deviation investigations, CAPA execution, and change control activities Complete all training activities required to maintain quality compliance. Maintain strict compliance with regulatory and internal quality standards Perform routine maintenance activities required for a GMP environment Skills and Experience We Look For Bachelor's degree in relevant scientific field and 2+ years of industry experience in manufacturing (cell therapy, biologics, or aseptic manufacturing environment) Familiarity with mammalian cell culture and aseptic techniques Ability to operate within a clean room environment for long duration Understanding of GMP principles and cleanroom operations Excellent organizational and prioritization skills Exceptional collaboration, communication, and interpersonal skills Flexibility to work weekends, holidays, or shift schedules as required Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The estimated base salary range for this position is $80,000 - $120,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

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External Conduct comprehensive vehicle-level functional testing of autonomous vehicles throughout all End-of-Line (EOL) processes. Engage in practical and professional communication with cross-functional teams. Comply with established processes and procedures. Provide regular updates on testing progress to leads and management personnel. Escalate any issues that impede testing procedures. Collaborate closely with engineers and fellow technicians on vehicle testing initiatives. Execute daily tasks to ensure project timelines are adhered to. Offer constructive feedback to team members to facilitate future development efforts. Maintain a clean and organized vehicles, equipment, and the build area, ensuring all Environmental Health and Safety guidelines are adhered to. Allocate approximately 50% of work time to driving vehicles under autonomous control. Identify opportunities for enhancement in Quality, Efficiency, and Safety standards. Demonstrate flexibility and a proactive approach in supporting evolving processes and assuming new responsibilities. Assist with paperwork and documentation related to vehicle readiness. Internal Assist with vehicle transportation and movement logistics. Troubleshooting issues consistently and generating accurate mission and ZPT reports. Communicating clearly and effectively in designated Slack channels, both verbally and in writing. Proactively reporting any issues encountered. Demonstrating a strong drive to learn new technologies, processes, and methodologies. Effectively multitasking and managing the complete mission lifecycle for multiple vehicles simultaneously. Being open to cross-training, supporting various processes, and assisting other teams and tasks. Following up on outstanding ZPTs and providing summaries or feedback. Possessing a thorough understanding of vehicle behavior, software, and firmware to independently perform diagnostics and root cause analysis with minimal Engineering support, while collaborating with engineers and cross-functional teams. Contributing to creating Manufacturing AST work instructions through close collaboration with Engineers and teammates. Demonstrating proficiency in navigating and utilizing various Manufacturing systems and tools such as TestRail, GitHub, Looker, CANalyzer, Vehicle Testers, MFG PSS, and Twilio. Performing vehicle bring-up procedures and executing necessary software/firmware updates to support Engineering and General Assembly. Working with new vehicle platforms (e.G, L3 and VH6) entails more critical and complex responsibilities, often requiring ASTs to be the first to troubleshoot new issues and validate fixes due to the initial absence of Work Instructions, prior to broader fleet deployment. Qualifications: Bachelor's degree with 4-6 years of experience in the autonomous vehicle industry. or High School Degree/GED with 8-10 years of experience Strong understanding of both mechanical and electrical systems. Proficient in interpreting technical documents, schematics, and diagrams. Skilled in using diagnostic tools and test equipment. Technical aptitude in firmware, software, and hardware. Excellent communication and problem-solving abilities. Positive attitude with a willingness to learn new tasks. Excellent driving history with a priority on safety. Preferred: Technical certification Experience in an R&D or manufacturing environment Familiarity with autonomous systems or advanced driver assistance systems (ADAS) Exposure to GitHub, TestRail, and other software tracking tools Work Environment: This role is situated within manufacturing and testing environments. Flexibility is essential due to potential periods of downtime and the need to support other teams to meet production and testing schedules. Adhere to all manufacturing safety policies. Physical Requirements: Ability to lift up to 25 lbs Standing, walking, and working in a manufacturing or shop environment for extended period