Manufacturing technician jobs in Pittsburg, CA

Job Title: Opto-Mechanical Assembly Engineer / Technician (1st and 2nd Shift) Work Schedule: On-site Rate: $36, Based on experience. Shift: Monday - Saturday 06 AM - 03:30 PM 03 / 04 PM or 12:30 - 02:30 AM (OT required) OT required on Saturday's Responsibilities: • Maintain tool schedules, complete alignment processes (milestones) per defined test times - work assignments that are moderately complex in nature where judgment is required in resolving problems • Support tool progression priorities -tests and troubleshoots assemblies and/or final systems • As required, prepares technical reports summarizing findings and recommending solutions to technical problems Additional Responsibilities: • Maintain test tooling, sending/receiving tooling to complete daily work activities (3rd party calibration) Top 3 Skills Needed: 1. Mechanical experience - hands-on mechanical work is essential. 2. Optical alignment experience - highly preferred. 3. Commitment for long-term - ability to work extended hours and sustain workload. Work Schedule: • 6 days/week (Monday-Saturday) • 10+ hours/day • Long-term engagement expected. Qualifications: • Minimum High School Diploma • At least 1 year of relevant experience (mechanical/optical) • Interview process will assess knowledge and skills. Interview Process: • 3 rounds in one day (~1.5 hours total): • Mechanical test • Written test • One-on-one interview Industry Preference: • Candidates from aeronautics or medical devices are good fits. • No fiber optics experience required. Requirements: • Performs the build, calibration, testing and troubleshooting of mechanical assemblies at a system level. • Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams. c. • Tests and troubleshoots assemblies and/or final systems. • May complete rework on assemblies and/or systems as a result of testing. • Prepares technical reports summarizing findings and recommending solutions to technical problems. May assist in the selection and set-up of specialized test equipment. • Requires experience in testing digital and/or analog systems • Ability to read complicated drawings, mathematics, handbook formulas, and a variety of testing and measuring instruments • An AA degree, military technical training or their equivalent vocational training is a +. • Will accept HS diploma with equivalent experience • Lift 50 lb requirement EXPERIENCE: • Typically requires a minimum of 2 - 4 years of related experience. • Looking for a person with strong mechanical, electrical and software skills. • NOT looking for PCB experience/ board TS. • More opto assembly BIG system level. About Maxonic: Since 2002 Maxonic has been at the forefront of connecting candidate strengths to client challenges. Our award winning, dedicated team of recruiting professionals are specialized by technology, are great listeners, and will seek to find a position that meets the long-term career needs of our candidates. We take pride in the over 10,000 candidates that we have placed, and the repeat business that we earn from our satisfied clients. Interested in Applying? Please apply with your most current resume. Feel free to contact Manish Rajput (****************** / *************** for more details.

***Shift schedule rotating 12-hour night shift from 6PM to 7AM. Wednesday to Saturdays. Alternating Saturdays*** PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.). TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents. QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.). BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics. WORK ENVIRONMENT/PHYSICAL DEMANDS • Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands. • Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds. • May require work around loud equipment. • The use of personal protective equipment will be required. • Requires various shift-based work and off hours. Skills • Strong communication skills-verbal and written • Ability to work in a team environment which includes good conflict resolution and collaboration • Displays good initiative to identify areas for improvement and implement solutions Education -Bachelor's degree in science related area or engineering -Associate's degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry

Are you an experienced Manufacturing Associate with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Manufacturing Associate to work at their company in Novato, CA. Primary Responsibilities/Accountabilities: PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes, including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.). TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents. QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.). BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track-wise, ERP, etc.). Support trending of defined department metrics. Qualifications: Bachelor's degree in science science-related area or engineering Associate's degree in science science-related area or a Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands. Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds. May require working around loud equipment. The use of personal protective equipment will be required. Requires various shift-based work and off-hours. Preferred: Strong communication skills-verbal and written Ability to work in a team environment, which includes good conflict resolution and collaboration Displays good initiative to identify areas for improvement and implement solutions

Senior Formulation Technician Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: Monday to Friday from 06:00 AM to 02:30 PM Pay Range: $20 to $26 per hour Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary Work in a team-based manufacturing laboratory environment responsible for synthesizing, testing, and qualifying ion exchange media used in chromatography consumables, while maintaining high quality, safety, and compliance standards. Responsibilities Perform testing and qualification of resin products using specialized instruments to meet customer and production demands. Accurately record, analyze, and report test results; maintain complete and compliant documentation. Execute complex production work orders in accordance with established SOPs and procedures. Analyze data, derive conclusions, and prepare technical reports based on findings. Collaborate with cross-functional teams to support production and quality objectives. Adhere to ISO 9001 guidelines, GMP, and corporate quality policies. Comply with EH&S safety requirements and participate in safety improvement initiatives. Identify process improvement opportunities and propose corrective or preventive actions. Maintain a clean, organized, and inspection-ready laboratory environment. Required Skills Hands-on experience in a chemistry or biotechnology laboratory. Bachelor's degree in Chemistry, Biotechnology, or a related life sciences field. Experience in a manufacturing or regulated production environment. Familiarity with chromatography techniques and chromatography-related software. Exposure to Lean Manufacturing, PPI, or Continuous Improvement tools. Willingness and ability to learn new processes, tools, and technologies. Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Ability to read, understand, and follow written SOPs and verbal instructions in English. Strong mathematical skills, including basic arithmetic with whole numbers, fractions, and decimals. Proficiency in Microsoft Word, Excel, Outlook, and basic data handling. Strong documentation, organizational, and problem-solving skills. Effective verbal and written communication skills. Familiarity with common hand tools (e.g., wrenches, torque drivers, tweezers). Ability to work independently with minimal supervision while meeting deadlines and production targets. Strong punctuality, attendance, and ownership mindset. Understanding of production schedules and task prioritization. Compliance with GMP, QSRs, ISO, and IVD regulatory requirements. TekWissen Group is an equal opportunity employer supporting workforce diversity.

We're seeking a hands-on, resourceful Lab Technician to help set up and maintain specialized equipment in a fast-paced materials and chemical research lab. This is an exciting opportunity to join a growing startup environment where creativity, independence, and problem-solving are key. You'll play a critical role in getting our lab fully operational from setting up utility and process equipment to performing light construction and installation work. The ideal candidate has a background in equipment maintenance and lab setup and is comfortable working with minimal supervision to troubleshoot and execute practical solutions. Key Responsibilities Unbox, assemble, and install laboratory and utility equipment. Anchor, mount, and set up equipment such as gas cylinder racks and chillers. Assist in connecting equipment exhausts to the building's HVAC system (HVAC knowledge a plus). Perform basic equipment maintenance and troubleshooting as issues arise. Work creatively to solve unexpected problems (e.g., adapting equipment connections, fittings, or power plugs). Collaborate with lab leadership to ensure equipment installations are completed safely and correctly. Communicate clearly with team members and management about progress, challenges, and recommendations. Qualifications Hands-on experience in equipment setup, maintenance, or facilities work in a lab, manufacturing, or semiconductor environment. Ability to work independently with minimal guidance in a startup or R&D lab setting. Comfortable with physical tasks such as unboxing, lifting, drilling, and anchoring equipment. Familiarity with compressed gas systems, chillers, and/or HVAC integration is highly desirable. Strong communication and problem-solving skills. Creative and resourceful approach to technical challenges. Additional Details Flexible scheduling during standard business hours. Opportunity for long-term or full-time conversion as lab operations scale. Location: Menlo Park, CA Submit resume to *********************** Owen Williamson ************ x127

Adecco is seeking Bilingual Production Warehouse Operators for immediate openings with a Client in San Francisco, CA. Weekly pay starting at $20.00 per hour and competitive benefits with options such as medical, dental, vision, and 401(k). As a Production Warehouse Operator, you will be responsible for performing a variety of warehouse tasks, including picking, packing, loading, and unloading products. You'll need to lift, carry, and move items weighing up to 50 lbs., and remain active throughout your shift by standing, walking, reaching (approximately 5'6”), and bending as needed. You will operate handheld scanners with training provided, follow all safety guidelines and procedures, maintain a clean and organized work area, and assist with general warehouse duties as assigned. These Production Warehouse Operator jobs require candidates have 1-2 years' experience, and the availability to work weekends. Spanish speaking a plus! Click on Apply Now to be considered for this Production job in San Francisco, CA. Pay Details: $19.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

About Applied Aerospace: Join the team that builds for the best. At Applied Aerospace, we design, fabricate, and test mission-critical aerospace components for leading innovators like SpaceX, NASA, Northrop Grumman, and Boeing. Every part we create reflects our relentless commitment to quality, reliability, and performance. Through precision engineering and purpose-driven innovation, we're helping take aerospace technology to new heights - and we're looking for talented individuals who want to be part of that journey. OVERVIEW OF POSITION: Our company is currently seeking a dedicated and detail-oriented Manufacturing Technician to join our team. This position involves the hand assembly and construction of various components, ensuring high-quality standards are met. The technician will work in accordance with the work instructions provided, requiring strong attention to detail and the ability to follow precise guidelines. ESSENTIAL JOB FUNCTIONS: * Hand assembles parts following detailed work instructions and technical diagrams. * Ensure strict adherence to quality specifications throughout the assembly process. * Inspect finished parts for defects and report any issues or deviations. * Collaborate with engineers, supervisors, and other team members to resolve problems. * Safely operates hand tools, power tools, and machinery required for assembly. * Maintain accurate and detailed documentation of assembly processes, work completed, and any deviations encountered. * Follow all safety protocols, guidelines, and regulations. GENERAL: * Ability to read and interpret work instructions and technical diagrams. * Excellent manual dexterity and hand-eye coordination. * Strong attention to detail and the ability to work with precision. * Effective verbal and written communication skills in English. * Ability to work independently as well as in a team environment. * Willingness to join and comply with union rules and regulations. * Preferred experience in assembly or manufacturing. * Ability to read and interpret blueprints and Mylar's. This job description is not intended to be all-inclusive. Employees may perform other related duties as assigned to meet the ongoing needs of the Company. Applied Aerospace is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. Applied Aerospace is committed to working with and providing reasonable accommodation to individuals with disabilities or individuals who may need religious or medical accommodation. If you need accommodation because of a disability, medical, or religious reason for any part of the employment process you can notify the Human Resources Department, and your request will be reviewed.

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

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

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

Working in a team of media process technicians, media process technician I will manufacture dehydrated and liquid cell culture media. Formulation technician will be able to follow batch record instructions and will be expected to weigh microgram to kilograms quantities of individual raw materials, calibrate equipment, follow safety policies and procedures, operate milling equipment, perform sterile filtration and any other tasks required to complete cell culture media manufacturing. Standard product testing, such as osmolality, pH and turbidity, will also be performed in this job. This position works closely with R&D, procurement, quality, process technology, marketing as well as external and internal customers and vendors RESPONSIBILITIES: Responsible for the staging and compounding of raw materials within weight tolerances (e.G. Micrograms to kilograms), milling, blending, aseptic liquid filling, process control monitoring and documentation of such procedures for manufacturing dehydrated culture media and liquid media in accordance with production schedules following the appropriate GMP and department procedures Completes all required documentation neatly, accurately, and in accordance with GMP. Performs cleaning, inspection, calibration and assists in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting. Handles raw materials per GMP and Safety requirements. Uses equipment such as pipettors, balances, osmometer, turbidimeter and pH meters. Ensure that tasks are performed in a safe and responsible manner to create an injury free and incident free workplace Required to follow through on assigned responsibilities and able to function under supervision. Responsible for promoting positive team environment through good communications and team engagement. May be required to work overtime. Performs other duties as assigned in support of business goals QUALIFICATION REQUIREMENTS: Minimum of High School Diploma or equivalent. Minimum of 6 months experience in a high-paced laboratory environment or manufacturing facility. Equivalent combination of education, training, and relevant work experience maybe considered. Must be able to read, write, and follow testing and inspection procedures. Must be able to maintain neat, accurate and complete records and logs. Mechanical aptitude and ability to disassemble and reassemble various equipment. Good communication skills and ability to work both individually and as part of a team. Flexibility with departmental work schedules including overtime. Must be able to focus with continuous attention to detail. Basic experience in weighing multiple components is required. Basic proficiency with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS Word and MS PPT is required. Statistical analysis using mathematical spreadsheets such as Excel or Minitab is highly desired. Must be able to lift or move approximately 40lbs Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

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

Mon-Fri 6a - 230pm Senior Formulation Technician Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a Key Responsibilities: • Perform testing and qualification of resin products on specialized instruments to meet customer demand. • Record and report test results accurately and maintain proper documentation. • Complete complex production work-orders according to established procedures. • Analyze data, derive conclusions, and prepare reports based on findings. • Collaborate with cross-functional teams. • Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. • Follow EH&S safety requirements and actively participate in safety improvement activities. • Continuously identify areas for improvement and propose countermeasures. • Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: • Knowledge of Good Laboratory and Manufacturing Practices and standards. • Proficiency in Microsoft Office: Excel, Word, PowerPoint. • Good mathematical, problem-solving, and organizational abilities. • Excellent communication skills (verbal and written). • Ability to read and understand written procedures (SOPs) and follow verbal instructions. • Strong punctuality and attendance record. • Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) • Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. • Ability to work independently with occasional assistance. • Ownership mentality and ability to meet established deadlines and targets. • Willingness to acquire new knowledge and skills. • Understanding of production schedules and ability to prioritize tasks accordingly. • Hands-on experience in a Chemistry laboratory is preferred. • Knowledges of Chromatography software a plus. Education • At least 1+ years of experience in manufacturing environment • A bachelor's in chemistry and or biotechnology preferred. Physical requirements: • Ability to lift and/or move up to 40 pounds. • Regularly required to stand; walk; use hands & finger to handle & feel. • Frequently required to sit and reach with hands and arms. • Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. • Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: • Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: • Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. • Ability to read and write English and understand instructions written or orally in English. • Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. • Knowledge of Word, Excel and Outlook. Job Type & Location This is a Contract position based out of Sunnyvale, CA. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sunnyvale,CA. Application Deadline This position is anticipated to close on Dec 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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

+ The consultant will perform advanced hands-on manufacturing operations in a cleanroom environment, supporting the production of semiconductor components, subassemblies, and final assemblies. + This role works closely with engineers on equipment setup, calibration, troubleshooting, rework, and quality testing. They will handle delicate wafer materials, operate lab equipment, and follow strict cleanroom, ESD, and quality standards while maintaining high productivity and precision. **Responsibilities:** + Perform hands-on manufacturing work in a cleanroom environment (≈95% of time) + Handle semiconductor wafers, including transferring from clamshells to FOSBs, following ESD and cleanroom protocols + Execute cleaning, inspection, assembly, measurement, and shipment preparation tasks + Set up, configure, and adjust lab equipment and modules to meet product and customer requirements + Support high-volume production while maintaining quality, precision, and attention to detail + Troubleshoot equipment and process issues; make adjustments to achieve specifications + Perform calculations and accurately record production and measurement data + Work independently and collaboratively, managing changing priorities and deadlines + Follow all safety, ISO, quality, and company procedures; lift materials up to ~25 lbs as required **Experience:** + 5+ years of manufacturing-related experience preferred + Ability to read, understand, and follow assembly and manufacturing documentation in full + Strong verbal and written communication skills + Familiarity with hand tools and machine tools + Strong troubleshooting and problem-solving skills + Knowledge of ESD practices and cleanroom protocols + Proficiency with Microsoft Word and Excel + Ability to lift approximately 25 lbs. using appropriate equipment if required + Must be comfortable working 100% onsite in a cleanroom environment **Skills:** + Manufacturing + Hand/Machine tool + Wafer **Education:** + Associate degree or equivalent technical training. **About US Tech Solutions:** 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 *********************** (********************************** . US Tech Solutions 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 status as a protected veteran.

Senior Formulation Technician Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: First Shift - 06:00 AM to 02:30 PM Pay Rate: $20 to $22 per hour Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: The Media Process Technician I works as part of a team to manufacture dehydrated and liquid cell culture media. The technician follows batch record instructions, weighs raw materials ranging from micrograms to kilograms, calibrates equipment, operates milling equipment, performs sterile filtration, and completes media manufacturing tasks. Responsibilities also include performing standard product testing (osmolality, pH, turbidity) and working closely with cross-functional groups such as R&D, procurement, quality, process technology, marketing, as well as internal/external customers and vendors. Responsibilities Stage and compound raw materials within specified weight tolerances (micrograms to kilograms). Perform milling, blending, aseptic liquid filling, and process control monitoring. Follow GMP and departmental procedures to manufacture dehydrated and liquid culture media according to production schedules. Complete all required documentation neatly, accurately, and in compliance with GMP. Perform cleaning, inspection, calibration, and assist in equipment maintenance; maintain logs and records. Troubleshoot equipment issues. Handle raw materials following GMP and Safety requirements. Use laboratory and production equipment (pipettors, balances, osmometer, turbidimeter, pH meters). Work safely to maintain an injury-free and incident-free workplace. Carry out assigned responsibilities under supervision. Promote a positive team environment through effective communication and engagement. Work overtime when required. Perform other duties as assigned to support business goals. Required Skills & Qualifications BS in Chemistry or related field (or equivalent combination of education, training, and experience). Minimum 6 months of experience in a high-paced chemistry lab or manufacturing environment. Ability to read, write, and follow testing and inspection procedures. Ability to maintain neat, accurate, complete records and logs. Mechanical aptitude; ability to disassemble and reassemble equipment. Good communication skills; able to work independently or as part of a team. Flexibility to work varying schedules, including overtime. Strong attention to detail and ability to focus on tasks continuously. Basic experience weighing multiple components. Basic computer skills, including MS Excel, Word, and PowerPoint. Ability to lift or move approximately 40 lbs. Desired Skills (Preferred but Not Required) Statistical analysis experience using Excel or Minitab. Experience handling multiple components and performing precise weighing. Familiarity with GMP environments, sterile filtration, and laboratory instrumentation. TekWissen Group is an equal opportunity employer supporting workforce diversity.

@HYVE Solutions, missions to help customers, business partners, and employees achieve success through shared goals, strategies, resources and technology solutions. Hyve Solutions is a leader in the data center solutions industry, designing, manufacturing, and delivering custom Server, Storage, and Networking Solutions to the world's largest Cloud, Social Media, and Enterprise companies. We pride ourselves on collaboration, innovation and thought leadership. Our team consists of diverse, forward-thinking individuals who dare to challenge the status quo, while working with many of the world's biggest customers. Hyve Solutions is a part of Synnex Corporation, a Fortune 500 company. Become part of a team that thrives on excellence in a fast changing, high-growth technology environment! Hyve Solutions is looking for a detail-oriented, hands-on, results-driven individual with proven communication skills and a strong work ethic to work in a challenging, fast-paced, energetic environment. Responsibilities: · Perform troubleshooting, repair, preventative and general maintenance on production tools and equipment · Work with vendors to troubleshoot and resolve equipment issues · Build and install tools and equipment to support factory requirements · Support Process Engineering team on programs and projects · Document equipment and tools issues, maintenance records, tooling logs and asset recording · Order parts and supplies to support production · Provide day to day tool and equipment support to production · Work with Production and Process Engineering to determine and recommend tool and equipment needs · Provide training to production and Process Engineering personnel as needed Qualifications: · Typically requires 2+ years of related experience and Associates degree or 4 years of related experience · Proficient in MS/Office (Word, Excel, etc.) · Mechanical aptitude, good with tools and working with your hands · Ability to lift 25lbs consistently · Work with precision tooling in small places · Understanding of general safety guidelines and practices · General knowledge of electro-mechanical functionality · Excellent communication skills Hourly Rate- $24.50 @ HYVE Solutions, we believe employees are our greatest asset and we empower them to make a difference in our business. Diversity and inclusion make us all better. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.

Mon-Fri 6a - 230pm Formulation Technician Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a Key Responsibilities: * Perform testing and qualification of resin products on specialized instruments to meet customer demand. * Record and report test results accurately and maintain proper documentation. * Complete complex production work-orders according to established procedures. * Analyze data, derive conclusions, and prepare reports based on findings. * Collaborate with cross-functional teams. * Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. * Follow EH&S safety requirements and actively participate in safety improvement activities. * Continuously identify areas for improvement and propose countermeasures. * Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: * Knowledge of Good Laboratory and Manufacturing Practices and standards. * Proficiency in Microsoft Office: Excel, Word, PowerPoint. * Good mathematical, problem-solving, and organizational abilities. * Excellent communication skills (verbal and written). * Ability to read and understand written procedures (SOPs) and follow verbal instructions. * Strong punctuality and attendance record. * Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) * Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. * Ability to work independently with occasional assistance. * Ownership mentality and ability to meet established deadlines and targets. * Willingness to acquire new knowledge and skills. * Understanding of production schedules and ability to prioritize tasks accordingly. * Hands-on experience in a Chemistry laboratory is preferred. * Knowledges of Chromatography software a plus. Education * At least 1+ years of experience in manufacturing environment * A bachelor's in chemistry and or biotechnology preferred. Physical requirements: * Ability to lift and/or move up to 40 pounds. * Regularly required to stand; walk; use hands & finger to handle & feel. * Frequently required to sit and reach with hands and arms. * Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. * Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: * Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: * Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. * Ability to read and write English and understand instructions written or orally in English. * Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. * Knowledge of Word, Excel and Outlook. Job Type & Location This is a Contract position based out of Sunnyvale, CA. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sunnyvale,CA. Application Deadline This position is anticipated to close on Dec 30, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Shift: Mon-Fri 6a - 230pm Duration: 12 Months Pay range: $28.00 Hourly - $28.00 Hourly Onsite Job Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. Key Responsibilities: •Perform testing and qualification of resin products on specialized instruments to meet customer demand. •Record and report test results accurately and maintain proper documentation. •Complete complex production work-orders according to established procedures. •Analyze data, derive conclusions, and prepare reports based on findings. •Collaborate with cross-functional teams. •Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. •Follow EH&S safety requirements and actively participate in safety improvement activities. •Continuously identify areas for improvement and propose countermeasures. •Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: •Knowledge of Good Laboratory and Manufacturing Practices and standards. •Proficiency in Microsoft Office: Excel, Word, PowerPoint. •Good mathematical, problem-solving, and organizational abilities. •Excellent communication skills (verbal and written). •Ability to read and understand written procedures (SOPs) and follow verbal instructions. •Strong punctuality and attendance record. •Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) •Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. •Ability to work independently with occasional assistance. •Ownership mentality and ability to meet established deadlines and targets. •Willingness to acquire new knowledge and skills. •Understanding of production schedules and ability to prioritize tasks accordingly. •Hands-on experience in a Chemistry laboratory is preferred. •Knowledges of Chromatography software a plus. Education •At least 1+ years of experience in manufacturing environment •A bachelor's in chemistry and or biotechnology preferred. Physical requirements: •Ability to lift and/or move up to 40 pounds. •Regularly required to stand;walk;use hands & finger to handle & feel. •Frequently required to sit and reach with hands and arms. •Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. •Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: •Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: •Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. •Ability to read and write English and understand instructions written or orally in English. •Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. •Knowledge of Word, Excel and Outlook. 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.