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Manufacturing Technician-6 month+ Contract- Mountain View, Ca


  • Help build and deploy our fleet of autonomous vehicles and robots
  • Assist in developing novel solutions on hardware prototypes
  • Assemble, install, and test mechanical and electrical components for use on our robots
  • Perform diagnostic troubleshooting and testing of our vehicle and robotics systems including electrical and mechanical sensors, cameras, computers, and other associated equipment
  • Take the initiative to understand, communicate, and resolve vehicle issues related to safety, hardware, or maintenance
  • Document all vehicle tasks and issues in our Fleet Tracking system


  • 4+ years of experience in Manufacturing
  • Bachelor’s Degree in Electrical or Mechanical Engineering
  • Detail oriented, highly organized, with a passion for learning
  • Diagnostic experience with vehicle or robotics systems such as electrical and mechanical devices, sensors, computers, and other associated equipment
  • Ability to remain flexible with the changing needs of the business
  • Experience working with High Voltage, EVs, or Autonomous Vehicles a plus
  • Automotive mechanic or hobbyist experience a plus
  • Electrical assembly, test, or manufacturing experience a plus
  • Electronic board soldering, experience in handling ESD sensitive components
  • Experience in extrusion lamination
  • Experience in flexible instrument or catheter assembly and testing
  • Proficiency in basic computer skills such as Word and Excel. Experience in SAP is a plus
  • Demonstrate the ability to effectively and clearly communicate concepts, ideas and knowledge to other individuals and teams
  • Experience working with ISO requirements and manufacturing scale-up processes
  • Cleanroom practice

Pay Rate-DOE/hr.

Please send resume to

Manufacturing Technician-Medical Device-Contract-Santa Clara, Ca

  • Materials and Inventory management for Pilot Line processes
  • Work Order and Non-conformance management for Pilot Line processes via ERP
  • Assemble various catheter designs and assist in developing design improvement, assembly approaches, and fixtures for articulating catheter devices.
  • Execute rework or deviation instructions with coordination with manufacturing engineering.
  • Identifies and escalates nonconforming products and supports root cause investigation alongside manufacturing engineering.
  • Perform testing, experimentation, and analysis.
  • Meet catheter Pilot Line yield and productivity goals.
  • Support processes and equipment qualification activities
  • Train manufacturing/Pilot Line operators and Technician processes and techniques
  • Assist manufacturing/Pilot line/process/R&D engineers in resolving product and process problems.
  • Complete documentation such as Lot History Records per GMP requirements
  • Support the introduction of new products onto the manufacturing line.
  • Follow GMP guidelines
  • Support experimentation to uncover key relationships between process variables and product performance.
  • Identifies and escalates nonconforming products and supports root cause investigation alongside manufacturing engineering
  • Provide day-to-day coordination and scheduling of floor activities with materials and planning Pilot Line teams.
  • Hands on Interview for New employees on Pilot Line.
  • Assist in the selection of new employees as required to meet business needs.
  • Provide timely feedback to employees on performance.
  • Communicate with staff on a regular and consistent basis as defined.
  • Keep management informed of issues & concerns in a timely manner.
  • Ensure staff are trained in all relevant procedures.
  • Ensure housekeeping standards are maintained within areas of charge.

Required Knowledge/Skills, Education, And Experience

  • ­­High school degree
  • 5+ years of experience with medical field or relevant companies is required.
  • Computer programs required; Ability to work with Excel, Word, Agile, SAP are preferred.
  • Have knowledge for end-to-end processes and have hands on skill set equivalent to operator III level.
  • Work on pilot line supporting new product development and able to build prototypes and provide feedback to engineers.
  • Support activities related to equipment qualification or process validation.
  • Able to execute protocols and document test results or draft work instructions.
  • Red line or create procedures electronically.
  • Able to perform simple failure analysis independently or assist engineers for more complicated failure analysis and able to provide feedback or ideas for continuous improvement.
  • Ability to work in a regulated environment in compliance to ISO 13485 and 21 CFR 820.

Pay Rate-30-35 DOE

Please send resume to

Robot Safety Technicians-San Carlos, Ca- and Gilroy, Ca – C2H


  • Primary role is to monitor, and if necessary, perform manual Emergency Stop of any robots operating outside their designed safety envelope
  • Familiarize yourself with the routine operations of multiple robot systems
  • Report Bugs/Issues if anomalous behaviors occur
  • Assist Service and Engineering in troubleshooting robots


  • 2+ years working in a Shop or Technical environment
  • Strong communication skills
  • Experience following Standard Operating Procedures is a plus
  • Experience with JIRA, Slack, and Confluence is a plus
  • Ability to speak Spanish is a plus


Please send resume to

Operators/Assembly-Medical Device-RWC or Santa Clara, Ca-Contract


Work in a clean room environment building multiple catheter products by following relevant Manufacturing Process Instruction (MPI). Follow a lean manufacturing process to achieve a daily build goal. Assist in building the next generation catheter products.

Core Job Responsibilities

  • Build catheters to meet the company sales goals
  • Meet catheter manufacturing yield and productivity goals
  • Assist manufacturing/process/R&D engineers in resolving product and process problems
  • Complete documentation such as Lot History Records per GMP requirements
  • Support the introduction of new products onto the manufacturing line
  • Follow GMP guidelines

Required Knowledge/Skills, Education, And Experience

  • ­­High school diploma
  • Able to perform multiple assembly processes for complex design. Processes involves combination of multiple disciplines and skill sets.
  • Able to handle and stuff multiple delicate components into shaft and assembly and glue small parts for integration.
  • Train other operators
  • Trouble shoot a failure
  • Able to perform complicated test, which involves using computational equipment, device setup/ alignment, and understand test results.
  •  Support engineering group to resolve line issues and able to provide improvement ideas.
  • Able to use common software for data collection or documentation such as MS excel and word.
  • Redline MPI’s and LHR’s for accuracy 
  • Flexible and have multiple skill sets to be able to work in pilot lines to support new product development.
  • Package product using pouch sealer and print labels using zebra printer.
  • Ability to work in a regulated environment in compliance to ISO 13485 and 21 CFR 820.

Work Environment

This position operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk; use hands to finger, handle or feel; and reach with hands and arms.

Position Type and Expected Hours of Work

This is a full-time position. Days and hours of work are flexible Monday through Friday, generally   6:00am to 2:30pm or 2:30-11pm.

Pay Rate-DOE

Please send resume to

IQC Inspector Role-Santa Clara, Ca-Medical Device-Contract


The IQC Inspector is responsible for performing incoming, first article and related activities. The candidate will utilize SAP to document Quality transactions as well as assist in compiling and trending quality data. 

 Core Job Responsibilities:

  • Perform inspections of purchased parts and subassemblies  according to specifications or standards using standard physical, mechanical and/ or electrical measurements.
  • Accurately document the results of the inspections and testing in SAP and on data sheets/forms as applicable.
  • Maintain all controlled document files and test records in a timely and accurate manner.
  •  Handle materials in accordance to procedures and prevent mix-ups, damage or other adverse effects.
  • Communicate inspection results to engineers and others  
  • Initiate and process Non-Conforming Material Reports when required.
  • Evaluate problems and make initial recommendations for possible corrective action to supervise.
  • Perform other duties as assigned by the Quality Management team.
  • Perform Gage R& R studies requested by engineers and others 

 Required Knowledge/Skills, Education, and Experience

  • Minimum HS diploma and practical experience.  AA or AS degree preferred.
  • 3+ years Quality Control experience in Receiving Inspection is preferred.
  • Previous work experience in a medical device or other related regulated industry is highly desirable.
  • Ability to read and comprehend engineering drawings and schematics.
  • Knowledge of Good Manufacturing Practices and Good Document Practices. 
  • Working knowledge of Geometric Dimensioning and Tolerance is highly desirable  
  • Working knowledge of measurement instruments.
  • Proficient using microscopes, visons systems (e.g. MicroVu, Smartscope, Optical Comparator) and conventional handheld inspections tools (i.e. calipers, micrometers, gage blocks etc.) 
  • Experience with CMM systems and electrical measurements a plus.
  • Must be able to work independently, prioritize activities and communicate well.
  • Basic computer skills, including MS Office Suite.
  • Previous experience with SAP preferred
  • Ability to work in a regulated environment in compliance to ISO 13485 and 21 CFR 820.
  • Must be able to lift a minimum of 25 lbs.

Pay Rate-DOE

Please send resume to

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