This position is responsible for the production of high quality cardiovascular medical devices on a team within a manufacturing cell. This position includes detailed assembly and operation of various equipment and machinery per documented procedures. This may include electronic assembly, casting/coating functions, mechanical assembly and packaging. Cleans tools and equipment per documented procedures. Disposes hazardous waste material on corresponding hazardous waste areas.
Duties;
Assembles medical devices and related components. Depending on work area, it may be a controlled cleanroom environment.
May include use of microscopes, use of hand tools, razor blades, syringes, soldering, adhesive bonding, and operating various equipment.
Performs routine assignments according to specified and/or standardized procedures. Work is closely and continually reviewed.
Performs visual inspection and precision measurements on components and assemblies.
Performs tests on units using computerized test equipment.
Repairs and corrects devices/components using microscopes and applicable tools.
Packages devices ensuring all parts are accurate and documentation is complete.
Maintains accurate records to ensure travelers, shop floor paperwork and quality documents are accurate, all parts are traceable, and quality issues can be addressed to assure the quality of all products.
Follows safety guidelines and utilize appropriate safety devices and equipment when performing all operations.
Participates in continuous improvement/quality initiatives to enhance production processes to achieve quality and profitability metrics.
Notifies supervisor or lead of the need to replenish supplies/materials and of any production difficulties that cannot be readily corrected.
Participates with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations.
Cooperates in keeping a clean, sanitary work environment throughout the building. Performs other related duties as directed or assigned.
Requirements:
Must be able to read, comprehend and follow English written procedures at a 6th grade level.
Must have good basic math skills at a 6th grade level.
Must be able to speak, follow verbal instructions and communicate effectively in English.
Possesses understanding of and ability to utilize electronic data collection systems and computer software packages.
Must have good dexterity to handle and maneuver small components and parts.
Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
Ability to make critical decisions and judgments with minimal supervision.
High school diploma required
2+ years of experience
$31k-39k yearly est. 1d ago
Production Packaging Associate- 3rd Shift-3
Altium Packaging, LLC
Manufacturing associate job in Tracy, CA
Include, but are not limited to the following:Demonstrates safe work practices by wearing correct PPE and following safety policies. Demonstrates punctuality and adheres to work schedule. Demonstrates a Teamwork attitude by working well and effective Packaging Associate, Production, 3rd Shift, Packaging, Associate, Manufacturing
$29k-38k yearly est. 6d ago
Manufacturing Specialist
Hydrogen Group
Manufacturing associate job in Hayward, 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)
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.
$25-31 hourly 1d ago
SMT Operator
ATR International 4.6
Manufacturing associate job in San Jose, CA
Job Purpose: Sets up and operates a variety of automatic or semi-automatic machines used in the production of the company's product Works from process sheets or written/verbal instructions given by supervisor to perform production tasks Checks and inspects operation against predetermined tolerances.
Nature of Duties/Responsibilities:
Must have experience to operate Fuji NXT, CP and IP machines.
Monitor the machine placement.
Capability to operate X-ray and MP3 machines.
Perform offline set up and solder paste printing process.
Interact with engineers on daily quality issues if any.
Requirement:
Education and Experience:
-1+ Years Experience as SMT operator in Manufacturing.
-Working Knowledge of the Procedure and Documentations.
-Ability to read and understand instructions to be assemble.
-Must be available for OT and weekend work as required in addition to minimum 40 hr./wk.
Benefits:
Benefits
Full-time employees (working an average of 30 hours or more) are eligible to select from different benefits packages Packages may include medical, dental, and vision benefits, a 401(k) retirement savings plan with employer match (available after 1 year of employment), commuter benefits, employee discount and referral programs, and life and supplemental income insurance Paid sick leave is provided in accordance with applicable state and local laws.
Compensation
Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience, as well as the benefits package you select.
Work Authorization
ATR International, Inc cannot sponsor work visas (H-1B, F-1 STEM OPT with I-983, or similar) Candidates must have valid U.S work authorization.
ATR International, Inc is an equal opportunity employer We celebrate diversity and are committed to creating an inclusive environment for all employees.
$33k-41k yearly est. 6d ago
Manufacturing Technician - Swing Shift
Red Oak Technologies 4.0
Manufacturing associate job in San Francisco, CA
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.
$30 hourly 2d ago
Manufacturing Technician
Clinlab Solutions Group
Manufacturing associate job in Alameda, CA
The position will actively contribute to manufacturing projects at the site. As part of the Cell Culture/Upstream Manufacturing group, you will have opportunities to work on and take ownership of a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into a GMP multi-product manufacturing facility. The role will support process monitoring, GMP readiness, and manufacturing activities. The scope of responsibilities may include but are not limited to document writing (SOPs, Equipment URSs, etc.), batch record testing and review, equipment validation execution support, and single-use assembly design.
Responsibilities:
Support upstream operations including but not limited to media prep; cell culture thaw, expansion, and cell banking; operation of single-use bioreactors, process monitoring, and harvest operations.
Performs internal support activities such as maintenance of analytical equipment, stocking of consumables, discarding expired reagents, and material coordination.
Maintains own training within compliance and trains other GMP associates upon completion of trainer qualification.
Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP Upstream activities.
Author/review/approve technical documents such as tech transfer protocols and reports, experimental plans, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs.
Documents work according to cGMP and cGDP.
Adheres to established regulations and follows cGMP established by site.
Maintain cleanroom standards, practices, and housekeeping according to SOPs.
Recognize any minor issues from the equipment and any affiliated documentation and take appropriate corrective action within scope. Notify leads/managers of issues and discrepancies immediately.
Assess impact of issues and non-conformities to products and projects as they pertain to product safety and efficacy or project milestones.
Evaluate new technologies and innovations to improve operational efficiency or expand cell culture capabilities.
Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control.
MSAT support, Material receipt, and inventory organization.
Other duties as assigned to ensure appropriate compounding practices.
Working Conditions:
This position is required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.
Qualifications:
BS in Engineering, Life Sciences, or related discipline with 1-2 years of relevant experience; AA degree with combination of industry experience and relevant degree; or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role.
Must have bioreactor operations experience.
Basic understanding of mammalian cell culture performance is required.
Experience with process monitoring software and equipment software (AVEVA/Wonderware) is a plus.
Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing.
Creative thinker that can identify better and more efficient methods to address issues and gaps.
Demonstrate ability to work independently and on cross-functional teams.
Ability to handle more than one task at a time, while maintaining attention to detail and working in a fast-paced environment.
Strong analytical skills and attention to detail.
Flexible mindset for a dynamic environment.
Flexibility with work hours to meet business needs, including weekends and holidays, as needed.
$35k-50k yearly est. 5d ago
Production Specialist/Engineer II
PTR Global
Manufacturing associate job in Cupertino, CA
mac OS Developer Mode: Hybrid Duration: Contract
We're looking for a creative and resourceful mac OS developer with 3-5 years of experience to support the lead engineer on a large internal tools project. This person will assist in implementing new features, testing existing code, and fixing bugs.
The project involves building internal extensions to a suite of established, consumer-facing mac OS applications. These extensions are designed to streamline the content creation workflows of our creative design and production teams.
The applications being extended have a mature and complex codebase, written predominantly in Objective-C (~90%). All new development is being done in Swift, with SwiftUI used for the user interface layer.
Success in this role will require deep knowledge of mac OS development and strong experience working across both Objective-C and Swift, including handling interoperability between the two. You should be comfortable navigating a large legacy codebase while contributing modern Swift code that integrates cleanly and safely.
A significant portion of this role will focus on testing new and existing features, as well as performing quick-turnaround bug fixes as the need arises.
Requirements
Extensive mac OS development experience with SwiftUI and AppKit
Deep knowledge of Swift and Objective-C interoperability, with hands-on experience working across both languages
Ability to extend and integrate with existing codebases while minimizing impact to legacy code
Proven experience contributing to large-scale, complex projects
Experience collaborating with creative and production teams, understanding their workflows and needs
Expert-level proficiency with Keynote, Numbers, and Pages
Exceptional debugging skills with a focus on writing clean, maintainable, and high- quality code
Strong communication and organizational skills - clear, concise, and proactive
Ability to work quickly and adapt to feedback from multiple stakeholders
Experience working in fast-paced, time-sensitive production environments
Self-motivated and capable of independently troubleshooting technical and process- related issues
Qualifications
Detail-oriented, organized, and thoughtful in the treatment of bugs, issue tracking, and QA processes
Ability to communicate technical concepts clearly and effectively to non-technical coworkers in language they can understand
Strong listening skills with the ability to interpret requests from creative and production teams, asking thoughtful clarifying questions when needed
Excellent problem-solving and analytical skills, with the ability to investigate, debug, and triage complex issues independently or collaboratively
Comfortable working in a fast-paced, informal environment, with the flexibility to respond to shifting priorities quickly and efficiently
Proven experience working on cross-functional projects, collaborating with diverse teams to achieve shared goals
About PTR Global: PTR Global is a leading provider of information technology and workforce solutions. PTR Global has become one of the largest providers in its industry, with over 5000 professionals providing services across the U.S. and Canada. For more information visit *****************
At PTR Global, we understand the importance of your privacy and security. We NEVER ASK job applicants to:
Pay any fee to be considered for, submitted to, or selected for any opportunity.
Purchase any product, service, or gift cards from us or for us as part of an application, interview, or selection process.
Provide sensitive financial information such as credit card numbers or banking information. Successfully placed or hired candidates would only be asked for banking details after accepting an offer from us during our official onboarding processes as part of payroll setup.
Pay Range: $50 - $60
The specific compensation for this position will be determined by a number of factors, including the scope, complexity and location of the role as well as the cost of labor in the market; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. Our full-time consultants have access to benefits including medical, dental, vision and 401K contributions as well as any other PTO, sick leave, and other benefits mandated by appliable state or localities where you reside or work.
If you receive a suspicious message, email, or phone call claiming to be from PTR Global do not respond or click on any links. Instead, contact us directly at ***************. To report any concerns, please email us at *******************
$50-60 hourly 5d ago
Production Specialist
Advantage Technical
Manufacturing associate job in Milpitas, CA
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.
$24 hourly 5d ago
Reagent Manufacturing Associate (RMA) II, Prenatal
Billiontoone 4.1
Manufacturing associate job in Union City, CA
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 ManufacturingAssociate (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)
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 ********************
$79.2k-84.5k yearly Auto-Apply 17d ago
Production Operator, General Labor - Starting at $27.48
Leprino Foods Company 4.7
Manufacturing associate job in Tracy, CA
Leprino Foods' history dates to over 65 years ago, when the Leprino family first started making small batches of mozzarella for local markets and eateries in Denver. We've grown a bit since then. Today, we are the largest manufacturer of mozzarella and lactose in the world, and a leading producer of whey protein. Still owned by the Leprino family, we've set our sights to become the "World's Best Dairy Food and Ingredient Company." To help us achieve that ambitious vision, we're looking for our secret ingredient: motivated individuals who are the absolute best at what they do. From three people in a small cheese shop in the early 1950s, we have grown to over 4,300 employees throughout our 16 global locations. Will you join us on our journey?
We are seeking a Production Operator to help us continue our successful trend in the global cheese and nutrition markets through quality of product and food safety at our Tracy, California production facility.
We have a competitive starting rate of pay for this role at $27.48 per hour. Upon completion of 90 working days, the hourly rate is $28.48
We Ask Of You To:
* The position requires the incumbent to feed and load cheese, fold bags, rework and re-dice, hand pack cheese and perform general housekeeping duties.
* The incumbent must be able to verbally communicate with their co-workers and promote good teamwork
* Must display recognition of quality control problems such as frozen/soft cheese, extraneous, and proper blend considerations
* Perform duties in a safe manner using Personal Protection Equipment (PPE)
* Maintain clean work area according to Good Manufacturing Practices (GMP) and safety policies
* Monitor cheese quality during packaging
* Product sort visually and using a metal detection system
* Record keeping
* Hand palletize product
* Operate Pallet Jacks: Manual and Motorized
* All other duties and responsibilities as assigned
You Have (Minimum Qualifications):
* Must be able to meet shift/schedule requirements
* Must be willing to work necessary Overtime as needed
* Must be at least 18 years old
* Must be able to speak, read, write, and comprehend basic English language
* Must be able to perform essential job functions of position with or without reasonable accommodation
A career with Leprino Foods means you'll be part of a worldwide family of individuals dedicated to producing high-quality products that help feed and nourish families around the world. Your contributions will be noticed and rewarded as you work to further our company, our customers, and one another. Apply today to learn more about our career path.
Leprino Foods celebrates and supports diversity. We believe in equal opportunity and do not discriminate on the basis of race, religion, ethnicity, national origin, gender, sexual orientation, age, marital status, veteran status, or disability. We know we are better together and are committed to creating an inclusive and supportive culture that leverages the unique talents, experiences, background, and perspectives of each individual employee
Leprino Foods Company utilizes the services of Psychemedics to perform our Hair Follicle Drug Testing. Additional information about this process can be obtained at ********************
Leprino Foods requires all individuals to wear the appropriate Personal Protection Equipment (PPE) as required by the role and location.
Leprino uses Psychemedics for a 90-day hair follicle drug test as part of the employee pre-employment process and also participates in E-Verify. All employees in our manufacturing facilities are required to wear Personal Protective Equipment (PPE) as mandated by their role and location.
$27.5-28.5 hourly 41d ago
Manufacturing Associate, Downstream
Asahi Kasei 4.3
Manufacturing associate job in Fremont, CA
The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team. Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings.
Company:
Bionova Scientific LLC
Job Description:
Company Summary:
Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems.
Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.
Position Summary:
The ManufacturingAssociate will actively contribute to the manufacturing and technology transfer projects at the Bionova Scientific Fremont location. As part of the Purification/Manufacturing group, you will have opportunities to work on a wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into the GMP manufacturing facility. The role will provide hands-on execution of complex experiments in a team setting. The role will support GMP and manufacturing activities.
Essential Duties and Responsibilities:
Execute, with oversight of qualified staff, complex unit operations including but not limited to chromatography, TFF, depth filtration, virus filtration, and buffer preparation in GMP manufacturing suites.
Maintain own training within compliance.
Support in equipment troubleshooting, pilot scale material generation, non-GMP tox material generation and GMP downstream manufacturing activities.
Author/review/approve technical documents such as tech transfer protocols and reports, production batch records, training materials, manufacturing SOPs, and regulatory filing documents per project needs.
Documents work according to cGMP and cGDP.
Adheres to established regulations and follows cGMP established by site.
Maintain cleanroom standards, practices, and housekeeping according to SOPs.
Recognize any minor issues from the equipment and notify leads/managers of issues and discrepancies immediately.
Contributes to quality activities such as investigations and area walk-throughs and support authoring deviations, CAPA, change control.
Other duties as assigned and flexible to work in shifts
Working Conditions:
This position required to work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.
Qualifications
Associate degree with 1-2 years of relevant experience, or combination of experience or relevant advanced degree, preferably in biopharma manufacturing role.
Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing, preferrable
Working knowledge of industry-standard purification processes (affinity, IEX, SEC, viral inactivation and filtration, depth filtration, TFF, UFDF, etc) and equipment (GE AKTAs, disposables), preferrable
Experience with process monitoring software and equipment software (UNICORN, Pi Historian)
Creative thinker that can identify better and more efficient methods to address issues and gaps
Demonstrate ability to work independently and on cross-functional teams
Ability to prioritize assignments and to manage multiple projects simultaneously.
Compensation Range: The base compensation range for this role is between $25 and $30 an hour. However, the actual compensation may vary depending on your experience and qualifications.
Health Benefits and Program: Bionova offers health benefits at a subsidized rate.
Healthcare, Dental, and Vision insurance
Life Insurance and Disability Program: 100% covered by Bionova.
Retirement Plan (401K) Up to 8% of Employer Match
Paid time off up to two weeks
10 days of Holidays and 5 days of Sick Leave.
As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.
$25-30 hourly Auto-Apply 10d ago
Manufacturing Associate II
Arcellx Inc. 4.0
Manufacturing associate job in Redwood City, CA
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 ManufacturingAssociate 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
$33k-43k yearly est. 54d ago
Manufacturing Plant Associate
McGrath 4.5
Manufacturing associate job in Stockton, CA
Job Description
The specific pay rate and level will depend on the successful candidate's qualifications, prior experience and location.
“Perks”
DailyPay Available!! Make any day a payday - You deserve to get paid any day!!
10 days + 2 half days Company Paid Holidays + vacation and sick time!
Medical, Dental, and Vision benefit options
401(k) Retirement Plan with Company Match.
Company paid Life Insurance
We also offer HSA, FSA, EAP and Pet Insurance!
Safety and Recognition programs
Boot Program
Drug-Free, Safety-Focused Work Environment
It's a great place to work where you are given the space to share ideas and opinions and the bottom-line is “YOU” matter!
“A Day in the Life”
In the Manufacturing Plant Staff personnel role, you will be responsible for general maintenance, general construction, and preparation of buildings for delivery to customer sites.
“What You'll Do"
Installation of structures or fixtures such as windows, frames, floorings, trim or hardware using hand or power tools per plan, drawings and to current relevant building code
Perform construction in the areas of carpentry, painting, flooring, ceiling, HVAC, roofing, demolition, drywall and other wall finish functions.
Shape or cut materials to specified measurements as noted on building plans or reasonably implied
Participate in and practice 5S and LEAN in the plan
Perform other duties as assigned
“Must Haves”
Is knowledgeable and follows the general procedures and safety measures
Able to work outside in variable weather conditions
Ability to use both manual and power tools and follow operating guidelines
Ability to use mathematics to calculate length, width, depth, etc. as it relates to construction and accuracy of specs and requirements
Ability to follow spoken and written instruction and work in fast paced construction environment with minimal guidance from leads or supervisors
Ability to safely perform all tasks, understand, and comply with Company's safety policies and procedures
Deliver a high-quality output consistent with the Company's construction standards
Able to take, record and follow standard measurements and cut or separate materials to specific measurements or quantities
Prior experience in construction, manufacturing, or other related work preferred
Special Considerations:
Position requires manual dexterity and the ability to maintain physical activity for most of the day
Must be able to lift up to 50 pounds and hold or lift a variety of objects
Able to carry, bend, stoop, turn, kneel, crawl, climb a ladder and other manual labor activities
Flexibility & Evolving Responsibilities
This job posting is intended to convey the general nature and level of work expected in the role. It is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee. Responsibilities may evolve over time, and team members may be asked to take on additional tasks or adjust their focus in response to changing business needs-sometimes with or without prior notice. This flexibility is a valued part of our culture and supports our commitment to collaboration, agility, and shared success.
McGrath will continue pre-employment drug testing including marijuana, even in states where it is legal, for this position which is classified as safety-sensitive within our construction operations and Drivers. Ensuring a drug-free environment is not only essential for the well-being of our team members but also aligns with regulatory requirements that govern safety-sensitive positions and commercial driving.
Pre-employment screenings are conducted after a conditional offer of employment is extended, in accordance with fair hiring laws. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, on the basis of disability and any other legally protected status. Our company uses E-Verify to confirm employment eligibility.
#ENV
$30k-38k yearly est. 1d ago
Manufacturing Technician Student
MacOm 4.5
Manufacturing associate job in Milpitas, CA
MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard.
MACOM has more than 75 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. Click here to view our facilities. In addition, MACOM offers foundry services that represent a key core competency within our business.
MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio.
About the Role
We are looking for a motivated and technically curious Manufacturing Technician Student to join our Product & Test Engineering organization. In this role, you will support engineers in developing, validating, and sustaining automated test solutions for high‑performance optical, RF, or semiconductor devices. This is a hands-on opportunity to learn how complex hardware and software test systems are built, debugged, and optimized in a fast-paced engineering environment.
You will work closely with senior test engineers, product engineers, hardware designers, and manufacturing teams to ensure robust, efficient, and scalable test solutions.
Key Responsibilities:
* Assist in developing and validating automated test scripts for die-level and module-level testing.
* Perform bench characterization, data collection, and basic analysis to support engineering experiments.
* Support test hardware bring-up, including probe cards, fixtures, interface boards, and instrumentation.
* Troubleshoot test stations, measurement anomalies, and equipment issues under guidance from senior engineers.
* Maintain test documentation, including procedures, change logs, and test correlations.
* Execute engineering experiments, collect data, and generate simple summary reports. Collaborate with cross-functional teams (hardware, software, product engineering, operations) to assist on ongoing engineering projects.
Preferred Skills & Qualifications:
* Working toward a B.S. or M.S. in Electrical Engineering, Computer Engineering, Physics, or related field.
* Basic understanding of electronic circuits and measurement principles, Semiconductor or optical devices (bonus), and test and measurement equipment (oscilloscopes, SMUs, VNAs, power supplies).
* Experience with Python, MATLAB, or LabVIEW for data analysis or automation.
* Ability to read and interpret schematics, datasheets, and test documentation.
* Strong analytical, debugging, and problem‑solving skills.
* Good communication skills and willingness to learn in a collaborative environment.
* Enthusiasm for hands-on work in a lab environment.
What You Will Learn
* Real-world test development processes, from concept to production.
* Automated test equipment and data acquisition systems.
* Bench characterization techniques for next-generation hardware products.
* How product engineering and test engineering drive yield, performance, and product quality.
* Cross-functional teamwork in a modern R&D/manufacturing environment.
The Salary for this position is $30 - $37 per hour. Actual salary offered to candidate will depend on several factors, including but not limited to, work location, relevant candidates' experience, education, and specific knowledge, skills, and abilities.
EEO:
MACOM is an Equal Opportunity Employer committed to a diverse workforce. MACOM will not discriminate against any worker or job applicant on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, genetic information, veteran status, military service, marital status, or any other category protected under applicable law.
Reasonable Accommodation:
MACOM is committed to working with and providing reasonable accommodations to qualified individuals with physical and mental disabilities. If you have a disability and are in need of a reasonable accommodation with respect to any part of the application process please call *************** or email HR_*************. Provide your name, phone number and the position title and location in which you are interested, and nature of accommodation needed, and we will get back to you. We also work with current employees who request or need reasonable accommodation in order to perform the essential functions of their jobs.
$30-37 hourly 7d ago
Manufacturing Associate
Ryco Staffing
Manufacturing associate job in Novato, CA
Job Description 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
$33k-46k yearly est. 17d ago
Manufacturing Associate
Real Staffing
Manufacturing associate job in Novato, CA
Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.
To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com
Job Description
One to the top pharmaceutical company is looking for 10 manufacturing professionals.
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, protein purification and formulation of bulk drug substance
Support initiatives for process optimization
Identify and elevate processing issues and support solutions
Demonstrated proficiency 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
Additional Information
All your information will be kept confidential according to EEO guidelines.
IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-727-5167 ASAP! I want to know more about your preferences.
If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!
$33k-46k yearly est. 60d+ ago
(CW) Manufacturing Associate (TEMPORARY)
Biomarin Pharmaceutical Inc. 4.6
Manufacturing associate job in Novato, CA
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
These positions are for the 6pm to 7am shift from Wednesday to Saturday, with every other Saturday off.
$28 hour
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
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, or protected veteran status and will not be discriminated against on the basis of disability.
In the U.S, the salary range for this position is $ 15 to $ 30 per hour. The base pay actually offered will take into account internal equity, and may also vary depending on candidate's geographic region, job-related knowledge, skills, and experience amongst other factors. The salary range for this position is: $15 to $30. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.
For additional benefits information, visit:
$15-30 hourly 60d+ ago
Additive Manufacturing Technician
Figure 4.5
Manufacturing associate job in San Jose, CA
Figure is an AI Robotics company developing a general purpose humanoid. Our Humanoid is designed for corporate tasks targeting labor shortages and jobs that are undesirable or unsafe. We are based in San Jose, CA and require 5 days/week in-office collaboration.
We are seeking a highly skilled Additive Manufacturing Technician to lead operations in our Prototype Additive Lab. You will work closely with engineering and manufacturing teams to support rapid iterative prototyping, tooling, and production needs for early-stage mechanical hardware.
Responsibilities:
* End-to-End Workflow: Manage the entire production cycle, including nesting parts to maximize build density, material loading, and managing complex print cycles.
* Machine Operation & Maintenance: Oversee the daily setup, operation, and preventative maintenance of all lab equipment and supplies.
* Post-Processing: Conduct secondary processes such as breakout/unpacking, cleaning, deburring, fastening, and final assembly.
* Design Feedback: Troubleshoot and resolve print failures, providing critical feedback to engineering teams to improve future designs for manufacturability.
Requirements:
* 2+ years of experience in a related industry
* Ability to understand complex engineering documentation and proficiency with 3D printing software
* Ability to tackle problems in which you may not have expert knowledge
* Must be able to work in a fast paced and collaborative environment
* Exceptional organizational, interpersonal, and communication skills
* Safety conscious, dependable, and a positive attitude
Bonus Qualifications:
* CATIA experience
* Fabrication
* Manual mill and lathe
* JIRA
The US base salary range for this full-time position starts at $40/hr.
The pay offered for this position may vary based on several individual factors, including job-related knowledge, skills, and experience. The total compensation package may also include additional components/benefits depending on the specific role. This information will be shared if an employment offer is extended.
$40 hourly Auto-Apply 13d ago
Manufacturing Technician
AASC 4.2
Manufacturing associate job in Stockton, CA
Our company is currently seeking a dedicated and detail-oriented General Production Laborer 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.
How much does a manufacturing associate earn in Dublin, CA?
The average manufacturing associate in Dublin, CA earns between $28,000 and $53,000 annually. This compares to the national average manufacturing associate range of $26,000 to $45,000.
Average manufacturing associate salary in Dublin, CA