Manufacturing associate jobs in Sunnyvale, 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.

Red Oak Technologies is a leading provider of comprehensive resourcing solutions across a variety of industries and sectors including IT, Marketing, Finance, Business Operations, Manufacturing and Engineering. Our client is an electronics manufacturer. They are looking for a Manufacturing Technician (Swing Shift) to join their team. This role is a CONTRACT position. Position will be ONSITE. Candidate must be able to commute onsite to San Francisco, CA. **Swing Shift - 2:00PM - 10:30PM - Monday through Friday - Some work on Saturday as needed** **Gated private parking lot available for contractors** **$30/hr - $35/hr** Position Requirements: Follow all Safety and Laser Safety procedures and requirements Be able to construct, test and calibrate engineering and production robotic and computer-controlled assembly systems using engineering prints, schematics, assembly instructions and engineering direction Knowledgeable in high precision measuring equipment, calibration, and detailed record generation Experienced and Proficient in the following: Mechanical hand and power tools Oscilloscopes, DMM, Signal Generators, Optics, Cameras Laser safety, lasers, laser pattern recognition, beam focus, and active alignment Auto dispense and cure of UV adhesive Multiple axis, vision assisted, computer controlled robotic assembly equipment in both a R/D and Volume Manufacturing environment Identification of “Root” Cause of Manufacturing, Quality and Yield issues Microsoft Office, Standard SPC and Flowcharts packages Pneumatic actuated Slides, Grippers, etc. Hex Pod Tables, Active Alignment Excellent reading, writing, and communication skills in English Minimum of 5 years industry experience, Lidar Sensor experience preferred but not required Be able to stand for long periods of time Lift and carry 35 lbs Red Oak Technologies is made up of people from a wide variety of backgrounds and lifestyles. We embrace diversity and invite applications from people of all walks of life. See what it's like to be at the top; connect with one of our recruiters and apply today. Red Oak Tech: Quality | Talent | Integrity Note: Compensation rates are based on years of experience and/or level of skills relevant to the opportunity.

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.

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.

Contract to Hire Milpitas, CA $24/HR - $28/HR (Depending on Experience) Responsibilities: Responsible for a variety of complex operations and duties in a production area. Develops, maintains and improves most assembly processes Evaluates process specifications periodically to determine if they accurately reflect the process requirements and reviews process steps and reduces inefficiencies Works with the Quality Engineers on process improvement, monitoring tools, root causes and corrective actions Drives production schedules and process related problems to closure Supports engineering and the development labs with all new product introduction and development Assists in the compliance of safety regulations, i.e. ISO and business controls Provides production ready documentation (MPIs) with equipment setup and programs Leads team in making process and efficiency improvements Handles first calls in non-maintenance down issues and provides assistance to manufacturing support with implementing changes Monitors equipment performance and makes minor adjustments such as set-ups, calibrations and alignments Clears minor machine difficulties and performs maintenance and repairs under supervision of technician, engineer or supervisor Assists operators by answering questions and demonstrating operations Spot checks product to ensure quality levels are maintained Stays current working with manufacturing support on process and equipment changes and upgrades Must have knowledge and experience with all assembly requirements Requirements: High school diploma / GED a minimum; Higher education is a plus 4+ years of related manufacturing experience and the ability to use complex equipment, read difficult instructions and maintain written records. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Demonstrated knowledge of manufacturing line techniques. Requires the ability to use complex equipment, read difficult instructions and schematics, and maintain written records. Good communication skills both verbal and written Use of the following tools may be required: Electronic Assembly: color code, component, loading, touch-up, commercial soldering, mechanical assembly, surface mount assembly, point to point wiring; Cables: crimping, harness assembly, connector/wire soldering, cable prepping; Testing: cable & harness testing, trouble shooting, component testing, logic analyzer; Inspection: bare board, systems, components, cable/harness, microscope, measuring tools; Machine Operations: automatic component insertion equipment, surface mount insertion equipment, wave soldering; Mechanical & Electrical Tools: power air guns, taps & dies, alignment tools, measuring tools; Office Skills: typing, telephones, Warehouse: forklift, electronic scales, pallet jack, staple gun, cycle counting, kitting.

Ready to redefine what's possible in molecular diagnostics? Join a team of brilliant, passionate innovators who wake up every day determined to transform healthcare. At BillionToOne, we've built something extraordinary-a culture where transparency fuels trust, collaboration drives breakthroughs, and every voice matters in our mission to make life-changing diagnostics accessible to all. We don't just aim for incremental improvements; we strive to build products that are 10x better than anything that exists today. Our people are our greatest asset: talented scientists, engineers, sales professionals, and visionaries united by an unwavering commitment to changing the standard of care in prenatal and cancer diagnostics. This is where cutting-edge science meets human compassion-every innovation you contribute helps remove fear of unknown from some of life's most critical medical moments. If you're driven by purpose, energized by innovation, and ready to help build the future of precision medicine, this is where you belong. We are looking for a Reagent Manufacturing Associate (RMA) II to join our growing superstar Process Engineering team responsible for producing molecular reagents used internally in our high throughput CLIA lab for patient testing. The RMA is responsible for working independently to make medium to high complexity reagents following established manufacturing protocols, contributing to production assignments and tasks with high quality and timely output. This is an onsite role. Responsibilities: Manufacture medium and high complexity reagents in a molecular manufacturing lab according to established SOPs. Operation of robotic laboratory equipment and traditional lab equipment (micropipettes, liquid handlers, thermal cyclers, centrifuges, sealers, sonicator, etc.) Use of traditional molecular biology processes and techniques (small volume pipetting, plating, quantitation, visual inspection) Maintaining thorough, accurate and detailed documentation of all work produced, including deviations Inventory management Collaboration with Research and Development for the scale-up and implementation of new reagent formulations. Lab maintenance such as labware cleaning and equipment maintenance as needed Daily completion of assigned tasks to keep manufacturing on track Qualifications: Bachelor's degree or equivalent degree in biology, chemistry, or clinical related sciences At least 6 months of experience with molecular biology techniques in a research or clinical laboratory Excellent attention to detail Effective written and verbal communication skills The ability to multitask and work independently Previous clinical laboratory experience is preferred Nice-To-Haves: Start-up experience Knowledge of medical genetics Experience in a cell-free DNA setting Familiarity with PCR or next-generation DNA sequencing laboratory experience Benefits And Perks: Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients Open, transparent culture that includes weekly Town Hall meetings The ability to indirectly or directly change the lives of hundreds of thousands patients Multiple medical benefit options; employee premiums paid 100% of select plans, dependents covered up to 80% Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%) Supplemental fertility benefits coverage Retirement savings program including a 4% Company match Increase paid time off with increased tenure Latest and greatest hardware (laptop, lab equipment, facilities) Free daily on-site lunches provided from top eateries A variety of perks on campus (state of the art gym, restaurant) Free on-site EV charging (compatible with all EVs, including Tesla) At BillionToOne, we are proud to offer a combination of a (1) base pay range (actual amount offered is based on experience and salary/equity options split that the candidate chooses), (2) generous equity options offering, (3) corporate bonus program, on top of (4) industry leading company benefits (free healthcare options, 401k match, very generous fully paid parental leave, etc.). For this position, we offer a total compensation package of up to $102,929 per year, including a base pay range of $79,200 - $84,480 per year. BillionToOne is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. For more information about how we protect your information, we encourage you to review our Privacy Policy. About BillionToOne BillionToOne is a next-generation molecular diagnostics company on a mission to make powerful, accurate diagnostic tests accessible to everyone. Our revolutionary QCT molecular counting technology enhances disease detection resolution by over a thousandfold using cell-free DNA-a breakthrough that's already transformed the lives of over half a million patients worldwide. Our Impact: We've pioneered game-changing diagnostic solutions that are redefining industry standards. Unity Complete™ stands as the only non-invasive prenatal screen capable of assessing fetal risk for both common recessive conditions and aneuploidies from a single maternal blood sample. In oncology, our Northstar liquid biopsy test uniquely combines treatment selection with real-time monitoring, giving oncologists unprecedented precision in cancer care. Our Growth: From $0 to $125 million in Annual Recurring Revenue in just four years. We've raised close to $400 million in funding, including a $130 million Series D round in June 2024, achieving a valuation of over $1 billion. This backing comes from world-class investors including Hummingbird, Adams Street Partners, Neuberger Berman, Baillie Gifford, and Premji Invest. Our Recognition: Forbes recently named us one of America's Best Startup Employers for 2025, and we were awarded Great Place to Work certification in 2024-with an incredible 100% of our people reporting they are willing to give extra to get the job done. These honors recognize not just our innovation but the exceptional culture we've cultivated-one that remains authentically collaborative and transparent even as we've scaled. Our Future: Headquartered in Menlo Park with facilities in Union City, California, we're continuing to push the boundaries of what's possible in molecular diagnostics. Recent clinical outcomes data for Unity Fetal Risk Screen and new advances in cancer diagnostics prove we're just getting started. At BillionToOne, you'll join a diverse team of passionate innovators who believe that the best science happens when brilliant minds collaborate openly, think boldly, and never lose sight of the patients whose lives depend on our work. Ready to help us change the world, one diagnosis at a time? Learn more at ********************

**School of Medicine, Stanford, California, United States** Research Post Date Nov 24, 2025 Requisition # 107807 **Manufacturing Associate - Stanford Center for Cancer Cell Therapy (CCT) (Onsite)** The Stanford Center for Cancer Cell Therapy (CCT) is seeking a Manufacturing Associate (PDM1) to perform clinical cell therapy manufacturing consistent with principles of current Good Manufacturing Practice (cGMP) and aligned with the clinical trial investigational phase for treating patients with incurable diseases. **Duties include*:** + Plan, prepare for and perform human clinical materials biomanufacturing campaigns typically as a verifier. Prepare final formulated cellular products for clinical trials within production timelines and manufacturing schedules. Mainly focused on CAR T cell therapies. + Train on biomanufacturing and cGMP procedures. + Plan and perform components of process development and technology transfer for manufacturing of clinical materials, scale-up/scale-out and optimization activities in transitioning and translating pre-clinical, benchtop research into phase appropriate clinical trials. + Perform upstream and downstream components of assigned cGMP projects. + Identify, document and report operating excursions and facility deficiencies; make recommendations for process improvements and documentation improvements including Standard Operating Procedures (SOP) and manufacturing Batch Records (BR). Document deviations and provide recommendations for Corrective and Preventative Actions (CAPA). + Contribute to detailed manufacturing budget; including sourcing, identifying and ensuring qualified and verified raw materials for manufacturing; outlining overall and per/patient costs for project materials and supplies. + Devise and revise methods and/or processes for SOP and Manufacturing Batch Records. + Independently track, verify and ensure cGMP grade raw materials for biomanufacturing. Identify and plan for supply chain and raw materials lead times for scheduled campaigns. + May prepare and submit abstracts or papers for publication in peer-reviewed journals and/or presentation at scientific conferences. Present results during internal meetings. _*- Other duties may also be assigned._ **DESIRED QUALIFICATIONS:** + Bachelor's degree in biology, bioengineering, chemistry or related scientific field. + Aseptic technique and cell culture experience is preferred. + cGMP experience is preferred. + Experience with CAR T, T cells, gene editing, and cell and gene therapy manufacturing is desired. + Ability to occasionally work into the evening and/or on weekends, depending on clinical manufacturing schedules. **EDUCATION & EXPERIENCE (REQUIRED):** Bachelor's degree in related scientific field or an equivalent combination of education and experience. **KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):** + General understanding of biological scientific principles. + Aseptic technique and mammalian cell culture experience. + General understanding on how to use laboratory equipment: biosafety cabinet, centrifuge, incubator, cell counter, micropipettes, etc. + General understanding of current Good Manufacturing Practice (cGMP) guidelines. + Computer skills and ability to learn quickly and master computer programs, databases and scientific applications. + Strong attention to detail. + Ability to work following Standard Operating Procedures (SOPs). + Ability to work in a cleanroom space donning special sterile gowning. + Ability to work under deadlines with minimal supervision. + Ability to maintain relationships and communicate effectively between multiple functional groups. + Excellent organizational skills and demonstrated ability to complete detailed work. **PHYSICAL REQUIREMENTS*:** + Frequently sit, grasp lightly, use fine hand manipulation, repetitive pipetting, perform desk-based computer tasks, and lift, carry, push, and pull objects up to 15 pounds. _*- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job._ **WORKING CONDITIONS:** + May require working in close proximity to blood borne pathogens. + Ability to work with unpredictable manufacturing schedules. + Position may at times require the employee to work with or be in areas where hazardous materials and/or infectious diseases are present. + Position requires working in a cGMP clean room environment. + Position may work with viruses: lentiviruses, adeno-associated viruses, and/or retroviruses. + Position may work with human embryonic stem cells (hESCs). + Employee must perform tasks that require the use of personal protective equipment, such as safety glasses and shoes, protective clothing and gloves, and possibly a respirator. + May be exposed to high voltage electricity, radiation or electromagnetic fields, lasers, noise > 80dB TWA, Allergens/Biohazards/ Chemicals, and confined spaces. + May require extended or unusual work hours based on clinical manufacturing requirements and business needs. May be required to stay at work until product is released. **WORK STANDARDS:** + Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. + Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors bases on training and lessons learned. + Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide,******************************* _The expected pay range for this position is $40.52 to $44.33 per hour._ _Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs._ _At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website (_ _***************************************************** _) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process._ _Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a_ _contact form_ _._ _Stanford is an equal employment opportunity and 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, protected veteran status, or any other characteristic protected by law._ _The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned._ Additional Information + **Schedule: Full-time** + **Job Code: 1015** + **Employee Status: Regular** + **Grade: F** + **Requisition ID: 107807** + **Work Arrangement : On Site**

Manufacturing Associate, DNA synthesis At Ansa Biotechnologies Emeryville, CA Our mission at Ansa Biotechnologies is to revolutionize the way we make DNA. Compared to reading or editing life's code, writing new code from scratch has remained one of the field's most elusive challenges. At Ansa, we are putting nature to work, creating novel enzymatic solutions that will redefine how we build DNA. We believe that the biggest challenges our world faces will be solved using biotechnology and that DNA synthesis is the fuel for that transformation. Our enzyme-based approach (published in Nature Biotechnology) promises to dramatically accelerate innovation in biological research and biotechnology, including therapeutics, diagnostics, biomanufacturing, and synthetic biology. We look forward to our DNA products making an impact. Currently hiring for day shift Sunday - Thursday. We believe lab automation facilitates novel synthetic biology applications through the synthesis of high-quality DNA at scale. In this role, you would accelerate the rate of discovery by developing and utilizing automated systems to dramatically impact synthetic biology. As one of the first members of our manufacturing team, you will have the opportunity to help build and support a growing and critical part of our operations. Beyond manufacturing, you will be a part of a dynamic, cross-functional, highly collaborative team operating at the interface between chemists, synthetic chemists, enzymologists, and automation experts. If you have a passion for the life sciences and the fundamental components of new technology, this job is for you! Responsibilities * Routinely start, purify and ship custom DNA oligonucleotide products using a novel enzymatic synthesis technology. * Leverage new protocols and implement into a rapidly scaling manufacturing pipeline working alongside a multidisciplinary team (manufacturing personnel, technology transfer & development departments). * Regular activities range from reagent and buffer preparation to cloning and cell culture purification work. * Operate using standard operating procedures (SOP) to execute a number of DNA synthesis equipment and sample traceability (LIMS) processes. * Work with teammates to design and scale next generation manufacturing systems for Ansas growing manufacturing platform. * Must be able to lift 50lbs and stand for long periods of time. * Collaborating in a team environment: At Ansa, communication between teams is critical-our technology is built on enzymes, chemistry, and automation. Additionally, we believe that honesty and openness are an instrumental part of the scientific endeavor. Experience * Comprehensive knowledge of and experience with molecular cloning and bacterial cell culture gained through education or hands on industry experience. * Working knowledge of liquid handling robots (ie. Hamilton, Tecan, Agilent Bravo) and other similar high throughput manufacturing tools. * Experience following SOPs and directions for both simple and highly complex processes. * Ability to learn and adapt quickly in a multidisciplinary environment with tight deadlines and specifications. * Excellent interpersonal and communication skills with the ability to clearly discuss and present technical concepts and results. * Commitment to demonstrating kindness, respect, and collaboration with a diverse set of colleagues of different backgrounds and disciplines. What We Offer: * Competitive hourly pay and equity. * Generous benefits package including health, dental, and vision. * Ongoing professional development and training opportunities. * A collaborative and innovative work environment. * The opportunity to be part of a company at the forefront of synthetic biology and innovation. San Francisco Bay Area Pay Range $27-$37.50/hr - Dependent upon experience

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

add

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.

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

As a Ryzen's Client manufacturing technician, you will be part of a team responsible for the assembly and testing of our vehicles. You will support both the build, performing defined test plans, and subassemblies. Being comfortable with mechanical, electrical, and computer systems is a plus. There will be regular use of hand, power and diagnostics tools along with custom equipment used to improve safety, quality, and reduce time. Your feedback from the build will go directly to your leads to help create and refine key systems and move Ryzen's Client towards mass production. Responsibilities Work closely with leads and other technicians on vehicle build Diagnose/Troubleshoot on-vehicle issues Complete daily tasks to ensure on-time completion of project Perform execution of on vehicle testing involving both hardware and software Provide feedback to necessary team members to assist in future development Regularly organize and maintain build area Work within all Environmental Health and Safety guidelines Identify areas of improvement of quality, efficiency, and safety Qualifications Bachelor's degree in Automotive Technology 4-6 years of experience working as a technician or in manufacturing environment Experience with basic hand and power tools Strong analytical and problem solving skills Understanding of basic electrical theory Familiar with electrical schematics and harness drawings Familiarity with CAN/LIN network systems Automotive/OEM experience is a plus Familiarity with Linux/Bash is a plus Computer Science knowledge is a plus Pay Rate: $25.00/HR - $35/hr

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 ************

Company Background Specter is creating a software-defined “control plane” for the physical world. We are starting with protecting American businesses by granting them ubiquitous perception over their physical assets. To do so, we are creating a connected hardware-software ecosystem on top of multi-modal wireless mesh sensing technology. This allows us to drive down the cost and time of deploying sensors by 10x. Our platform will ultimately become the perception engine for a company's physical footprint, enabling real-time perimeter visibility, autonomous operations management, and “digital twinning” of physical processes. Our co-founders Xerxes and Philip are passionate about empowering our partners in the fast-approaching world of physical AI and robotics. We are a small, fast-growing team who hail from Anduril, Tesla, Uber, and the U.S. Special Forces. Role + Responsibilities Specter is hiring a Manufacturing Technician to help assemble, test, and prepare our sensor and compute hardware for deployment in the field. You'll work hands-on with circuit boards, power systems, and enclosures - supporting both rapid prototyping and pilot production. This role is critical to ensure our hardware is built correctly, repeatably, and ready for scaling into the field. Potential Responsibilities Include: Assemble and test computer, electronic, and sensor hardware, including circuit boards, cables, and enclosures Follow and help improve build instructions, wiring diagrams, and test checklists Perform basic soldering, crimping, and connector assembly Use diagnostic tools (multimeter, oscilloscope, power supply) to verify system function Identify and resolve assembly or component issues in collaboration with engineers Track parts, builds, and materials using internal inventory systems Support prototype and pilot builds alongside mechanical and electrical engineers Maintain a clean, organized, and safe workspace Occasionally assist with deployment prep and on-site assembly or troubleshooting Qualifications 1-3 years of experience in electronics, computer hardware, or electro-mechanical assembly Comfortable with tools like screwdrivers, torque drivers, soldering irons, crimpers, and test meters Familiar with reading wiring diagrams or basic electrical schematics Detail-oriented and process-driven, with a focus on build quality and repeatability Strong hands-on troubleshooting and problem-solving skills Comfortable working in a fast-paced, high-iteration environment Bonus: experience with PCBA rework, cable harnesses, or ruggedized hardware assemblies Why Specter You'll be part of a small, mission-driven team building the foundation of real-world autonomy - the systems that let enterprises see, understand, and protect their physical operations in real time. If you love assembling things that matter, turning prototypes into reality, and working closely with engineers building the future of physical AI - we want to hear from you.

R&D Partners is seeking to hire a Manufacturing Technician in Redwood City, CA. Your main responsibilities as a Manufacturing Technician: In addition to the general description of the parent profile role for this job function, the following summarize key result areas, specific accountabilities and / or tasks, etc. associated with this job title include: Wear appropriate task-based and general PPE Ensures adherence to safety, health and environmental standards and guidelines, Good Manufacturing Practice and Order Due Date Supports manufacturing team to achieve operational delivery against defined production and quality targets Ensures raw materials and products meet the agreed product specification and production schedule Performs preventative maintenance on small equipment (heat sealer, mixers, conductivity meters, etc.) Provides routine support to department and other aligned support services to deliver line performance and continuous improvement projects Assists in setting up and running line equipment in accordance with the agreed settings/parameters Provides assistance to projects as needed, adhering to timelines to support project managers as necessary Participates in formal and informal training to meet business needs Performed other related tasks as assigned by Lead or Manager What we are looking for in a Manufacturing Technician: Essential HS Diploma GMP experience (1-3 years) Desirable Foundation level experience in production environment Experience with Good Manufacturing Practice Work experience in a regulated industry Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance PPO, HMO & HSA Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Pay Scale: Up to $48,547.20 (Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

Manufacturing Associate - Stanford Center for Cancer Cell Therapy (CCT) (Onsite) The Stanford Center for Cancer Cell Therapy (CCT) is seeking a Manufacturing Associate (PDM1) to perform clinical cell therapy manufacturing consistent with principles of current Good Manufacturing Practice (cGMP) and aligned with the clinical trial investigational phase for treating patients with incurable diseases. Duties include*: * Plan, prepare for and perform human clinical materials biomanufacturing campaigns typically as a verifier. Prepare final formulated cellular products for clinical trials within production timelines and manufacturing schedules. Mainly focused on CAR T cell therapies. * Train on biomanufacturing and cGMP procedures. * Plan and perform components of process development and technology transfer for manufacturing of clinical materials, scale-up/scale-out and optimization activities in transitioning and translating pre-clinical, benchtop research into phase appropriate clinical trials. * Perform upstream and downstream components of assigned cGMP projects. * Identify, document and report operating excursions and facility deficiencies; make recommendations for process improvements and documentation improvements including Standard Operating Procedures (SOP) and manufacturing Batch Records (BR). Document deviations and provide recommendations for Corrective and Preventative Actions (CAPA). * Contribute to detailed manufacturing budget; including sourcing, identifying and ensuring qualified and verified raw materials for manufacturing; outlining overall and per/patient costs for project materials and supplies. * Devise and revise methods and/or processes for SOP and Manufacturing Batch Records. * Independently track, verify and ensure cGMP grade raw materials for biomanufacturing. Identify and plan for supply chain and raw materials lead times for scheduled campaigns. * May prepare and submit abstracts or papers for publication in peer-reviewed journals and/or presentation at scientific conferences. Present results during internal meetings. * - Other duties may also be assigned. DESIRED QUALIFICATIONS: * Bachelor's degree in biology, bioengineering, chemistry or related scientific field. * Aseptic technique and cell culture experience is preferred. * cGMP experience is preferred. * Experience with CAR T, T cells, gene editing, and cell and gene therapy manufacturing is desired. * Ability to occasionally work into the evening and/or on weekends, depending on clinical manufacturing schedules. EDUCATION & EXPERIENCE (REQUIRED): Bachelor's degree in related scientific field or an equivalent combination of education and experience. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): * General understanding of biological scientific principles. * Aseptic technique and mammalian cell culture experience. * General understanding on how to use laboratory equipment: biosafety cabinet, centrifuge, incubator, cell counter, micropipettes, etc. * General understanding of current Good Manufacturing Practice (cGMP) guidelines. * Computer skills and ability to learn quickly and master computer programs, databases and scientific applications. * Strong attention to detail. * Ability to work following Standard Operating Procedures (SOPs). * Ability to work in a cleanroom space donning special sterile gowning. * Ability to work under deadlines with minimal supervision. * Ability to maintain relationships and communicate effectively between multiple functional groups. * Excellent organizational skills and demonstrated ability to complete detailed work. PHYSICAL REQUIREMENTS*: * Frequently sit, grasp lightly, use fine hand manipulation, repetitive pipetting, perform desk-based computer tasks, and lift, carry, push, and pull objects up to 15 pounds. * - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. WORKING CONDITIONS: * May require working in close proximity to blood borne pathogens. * Ability to work with unpredictable manufacturing schedules. * Position may at times require the employee to work with or be in areas where hazardous materials and/or infectious diseases are present. * Position requires working in a cGMP clean room environment. * Position may work with viruses: lentiviruses, adeno-associated viruses, and/or retroviruses. * Position may work with human embryonic stem cells (hESCs). * Employee must perform tasks that require the use of personal protective equipment, such as safety glasses and shoes, protective clothing and gloves, and possibly a respirator. * May be exposed to high voltage electricity, radiation or electromagnetic fields, lasers, noise > 80dB TWA, Allergens/Biohazards/ Chemicals, and confined spaces. * May require extended or unusual work hours based on clinical manufacturing requirements and business needs. May be required to stay at work until product is released. WORK STANDARDS: * Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations. * Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors bases on training and lessons learned. * Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, ******************************* The expected pay range for this position is $40.52 to $44.33 per hour. Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website (***************************************************** provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process. Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form. Stanford is an equal employment opportunity and 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, protected veteran status, or any other characteristic protected by law. The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned. Additional Information * Schedule: Full-time * Job Code: 1015 * Employee Status: Regular * Grade: F * Requisition ID: 107807 * Work Arrangement : On Site

Manufacturing Associate, DNA synthesis At Ansa Biotechnologies Emeryville, CA Our mission at Ansa Biotechnologies is to revolutionize the way we make DNA. Compared to reading or editing life's code, writing new code from scratch has remained one of the field's most elusive challenges. At Ansa, we are putting nature to work, creating novel enzymatic solutions that will redefine how we build DNA. We believe that the biggest challenges our world faces will be solved using biotechnology and that DNA synthesis is the fuel for that transformation. Our enzyme-based approach (published in Nature Biotechnology) promises to dramatically accelerate innovation in biological research and biotechnology, including therapeutics, diagnostics, biomanufacturing, and synthetic biology. We look forward to our DNA products making an impact. Currently hiring for day shift Tuesday - Saturday. We believe lab automation facilitates novel synthetic biology applications through the synthesis of high-quality DNA at scale. In this role, you would accelerate the rate of discovery by developing and utilizing automated systems to dramatically impact synthetic biology. As one of the first members of our manufacturing team, you will have the opportunity to help build and support a growing and critical part of our operations. Beyond manufacturing, you will be a part of a dynamic, cross-functional, highly collaborative team operating at the interface between chemists, synthetic chemists, enzymologists, and automation experts. If you have a passion for the life sciences and the fundamental components of new technology, this job is for you! Responsibilities * Routinely start, purify and ship custom DNA oligonucleotide products using a novel enzymatic synthesis technology. * Leverage new protocols and implement into a rapidly scaling manufacturing pipeline working alongside a multidisciplinary team (manufacturing personnel, technology transfer & development departments). * Regular activities range from reagent and buffer preparation to cloning and cell culture purification work. * Operate using standard operating procedures (SOP) to execute a number of DNA synthesis equipment and sample traceability (LIMS) processes. * Work with teammates to design and scale next generation manufacturing systems for Ansas growing manufacturing platform. * Must be able to lift 50lbs and stand for long periods of time. * Collaborating in a team environment: At Ansa, communication between teams is critical-our technology is built on enzymes, chemistry, and automation. Additionally, we believe that honesty and openness are an instrumental part of the scientific endeavor. Experience * Comprehensive knowledge of and experience with molecular cloning and bacterial cell culture gained through education or hands on industry experience. * Working knowledge of liquid handling robots (ie. Hamilton, Tecan, Agilent Bravo) and other similar high throughput manufacturing tools. * Experience following SOPs and directions for both simple and highly complex processes. * Ability to learn and adapt quickly in a multidisciplinary environment with tight deadlines and specifications. * Excellent interpersonal and communication skills with the ability to clearly discuss and present technical concepts and results. * Commitment to demonstrating kindness, respect, and collaboration with a diverse set of colleagues of different backgrounds and disciplines. What We Offer: * Competitive hourly pay and equity. * Generous benefits package including health, dental, and vision. * Ongoing professional development and training opportunities. * A collaborative and innovative work environment. * The opportunity to be part of a company at the forefront of synthetic biology and innovation. San Francisco Bay Area Pay Range $27-$37.50/hr - Dependent upon experience

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