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
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
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
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 17h 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. 17h ago
Manufacturing Technician
Insync Staffing 4.4
Manufacturing associate job in Campbell, CA
Pay $35-38
6 month+ assignment
Onsite in Campbell, CA
Assemble fluidic tube sets, mechanical gear, and catheter-based devices in a clean room environment through adhesive bonding and cure, mechatronic assembly and electrical/mechanical testing.
Demonstrated history of working on complex mechanical and electrical systems.
• HS diploma and a minimum of 8 years related experience; AA degree and a minimum of 5 years experience preferred.
• Strong understanding of assembly and calibration methods.
• A proven ability to work well in a team environment
• Must be capable of working independently and in a team while being flexible and self-motivated.
• Previous experience assembling Medical Devices in an FDA-regulated environment is preferred.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Assemble complex mechanical systems that encompass hundreds of unique parts. Your expertise with precision tools will ensure the accurate placement of linear guides, rotary bearings, actuators, motors, and drive systems.
• Collaborate closely with engineers to develop work instructions, maintain inventory for development builds, and ensure a clean and organized build environment.
• Maintain and calibrate tools, replenish stock fasteners, and ensure organization in the development and build areas.
• Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy.
• Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, and applicable FDA and Regulatory requirements.
• Actively promote and support the company's Management Review process.
• Inform responsible personnel of concerns involving product quality.
Benefits (employee contribution):
Health insurance
Health savings account
Dental insurance
Vision insurance
Flexible spending accounts
Life insurance
Retirement plan
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
$32k-41k yearly est. 1d 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 17h 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 11d 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 II
Arcellx 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. Auto-Apply 60d+ 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.
$33k-44k yearly est. 11d ago
Manufacturing Associate - Biotech
Lancesoft 4.5
Manufacturing associate job in Vacaville, CA
Title: ManufacturingAssociate - Biotech Duration: 12 Months Shifts and Hours schedule: Upstream Day Shift: 6am - 7pm Upstream Night Shift: 6pm - 7am Downstream Day Shift: 6: 30am - 7: 30pm Downstream Night Shift: 6: 30pm - 7: 30am
- These roles follow a 3-4-3 shift pattern
Description:
Role Purpose:
The ManufacturingAssociate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
20% Attain qualification for all assigned tasks and maintain individual training plan
10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
10% Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
High School Diploma or Equivalent minimum;AS/BS preferred
Preferred area of study: Science related discipline
0-3 years experience;some prior experience in a manufacturing setting preferred.
Proven logic and decision making abilities, critical thinking skills
$31k-40k yearly est. 6d ago
Remanufacturing Technician
Figure 4.5
Manufacturing associate job in San Jose, CA
Figure is an AI Robotics company producing a general purpose humanoid. Our Humanoid is designed for corporate or in-home tasks targeting labor shortages and jobs that are undesirable or unsafe. We are based in San Jose, CA and require 5 days/week in-office collaboration. We are looking for a Manufacturing Repair Technician to compliment our superstar team building and improving the product of the future.
Responsibilities:
Repairing full robots and smaller sub-assemblies for F.03 high volume manufacturing
Diagnosing electrical, mechanical, and software issues.
Document issues found, steps taken, and root cause of all repairs.
Validating and improving repair procedures for repeat issues and future remanufacturing of failed in field robots and sub-assemblies
Supporting any immediate need to keep manufacturing moving at a high rate
Requirements:
3+ years experience working with complex systems
Familiarity with computer based tools such as but not limited to Google Suite, Confluence, Jira, and an interest to learn command prompt and product specific software
Comfortable using a Digital Multi Meter
Familiarity with torque tools and mechanical assembly
Ability to follow assembly documentation
Ability to build with little to no documentation with engineering support
Complex system diagnostic ability
Great attitude and excited to face challenges
Bonus Qualifications:
Manufacturing experience
Computer based design experience
Automotive experience
Fabrication experience
Soldering experience
Small brushless motor experience
Robotics experience
The US base pay range for this full-time position is between $35 - $55 per hour.
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.
$30k-39k yearly est. Auto-Apply 43d ago
Manufacturing Bioprocess Technician
Us Tech Solutions 4.4
Manufacturing associate job in South San Francisco, CA
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Duties:
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for Cell Culture Purification that may include process monitoring, sampling, harvesting, purification, formulation and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP).
Essential Technician:
Operate systems that clean and sterilize tanks and filtration systems.
Prepare solutions for the production process.
Review documentation and check all calculations (e.g. tickets, labels, equipment reading).
Trouble shoot equipment and process problems.
Comply with safety requirements, cGMP, SOP and manufacturing documentation.
Use of automation to perform production operations.
Provide support to Manufacturing to meet production demands.
Operate automated systems for equipment operation.
Assemble and prepare equipment for production.
Exhibit detail oriented documentation skills
Communicate effectively and ability to work in a team environment.
Exhibit professional interpersonal skills.
Work with coworkers and supervisor to effectively troubleshoot minor equipment and process issues.
Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt.
Job Matrix
A good working knowledge of biopharm technology and processes.
Trained and skilled in all operational procedures of at least one manufacturing department.
Demonstrated ability to independently document and record information related to the process.
Occasionally makes routine decisions based on experience. Identifies and suggests solutions to common basic problems.
Recognizes non-routine problems, investigates and suggests potential solutions.
Judgment is required in resolving problems and making routine recommendations.
Ability to recognize deviation from accepted practices is required.
Supplementary Responsibilities:
Operate bioreactors, centrifuges, other harvest systems and protein purifications units.
Operate and clean fixed tank and filtration systems
Operate large scale column chromatography systems.
Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L bioreactors; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations.
Perform Solution Preparation activities (media and buffer make-up)
Clean, assemble, and sterilize equipment using glass washers and autoclaves.
Perform automated CIP and SIP of fixed equipment.
Qualifications
Degree in Life Sciences or engineering and 1 year related experience
Or Associate Degree and 3 year experience
Or High school and 5 years' experience
Biotech certificate from approved program
Additional Information
Sneha Shrivastava
Sr Technical Recruiter
862 - 579 - 4236
$35k-44k yearly est. 60d+ ago
manufacturing Technician
Artech Information System 4.8
Manufacturing associate job in Emeryville, CA
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
************
$35k-45k yearly est. 7h ago
Manufacturing Associate - Upstream
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 projects at the Bionova Scientific West Warren site. As part of the Cell Culture/Manufacturing group, you will have opportunities to work on wide-ranging set of projects for troubleshooting and investigations, system and workflow implementation, and tech transfers of processes into a GMP mulit-product 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:
Executes with oversight of qualified staff complex unit operations including but not limited to media prep; cell culture thaw, expansion, and end of production 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, material coordination and weigh and dispense.
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 manufacturing 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.
Other duties as assigned to ensure appropriate compounding practices
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
Minimum of Associate degree with 1-2 years of relevant experience, or combination of experience and relevant advanced degree, preferably in biopharma manufacturing role.
Must have bioreactor operations experience.
Understanding of mammalian cell culture performance is required.
Working knowledge of cGMP compliance as it pertains to procedures, processes, and manufacturing
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 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.
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 11d 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 Technician-2nd shift
AASC 4.2
Manufacturing associate job in Stockton, CA
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.
How much does a manufacturing associate earn in Livermore, CA?
The average manufacturing associate in Livermore, 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 Livermore, CA