Calyxo
Calyxo21d ago
$125,000 – $135,000/yr

Manufacturing Engineer – Capital - Pleasanton, CA

EngineeringManufacturing EngineerManufacturing & Production
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Quick Summary

Overview

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year.

Requirements Summary

Education: Bachelor of Science in Engineering or a combination of relevant education and experience 5+ years’ experience supporting medical device manufacturing Experience with electronic components/assembly in the context of medical device capital…

Technical Tools
ms-office

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.

Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.

The Manufacturing Engineer supports the development, improvement, and sustainment of manufacturing processes for CVAC 2.0, with a focus on quality, efficiency, and scalability. This role collaborates cross‑functionally with R&D, Quality, and Manufacturing teams to implement process improvements, support production, and transition new products and processes into manufacturing. The position also contributes to documentation, validation, equipment support, and continuous improvement while ensuring regulatory compliance and product quality.

  • Support technical projects leading to new/improved processes for CVAC 2.0.
  • Collaborate cross-functionally with R&D, Quality, Manufacturing Assemblers/Technicians, and other functional areas to design and develop processes to optimize robustness and flow, reduce costs and variability, and improve capability.
  • Contribute to the design and development of manufacturing procedures, tooling, and fixtures that result in sufficient capacity to meet customer demand while also promoting product quality, process efficiency, and operator safety.
  • Provide sustaining production line support including, but not limited to, implementing process improvements, troubleshooting equipment, and addressing operator inquiries.
  • Train and support production personnel during transition of new products/processes to production.
  • Create and update high-quality manufacturing process documentation and assure that processes and documentation follow established policies and procedures.
  • Apply LEAN, Six Sigma, and other best practice tools and principles for day-to-day problem solving and continuous improvement.
  • Assist in identifying equipment needs on the production floor and evaluating internal and external options for sourcing such equipment.
  • Generate and modify component/assembly/equipment drawings using Solidworks.
  • Support the execution of process and equipment validations (IQ/OQ/PQ).
  • Coordinate with external vendors as needed.
  • Perform routine equipment maintenance by following manufacturer’s instructions and established procedures.
  • Communicate project status, schedule baselines, schedule issues, project risks, and major decisions across all company disciplines.
  • Support product quality and support regulatory compliance.
  • Principal Manufacturing Engineer

Requirements

~1 min read
  • Education: Bachelor of Science in Engineering or a combination of relevant education and experience
  • 5+ years’ experience supporting medical device manufacturing
  • Experience with electronic components/assembly in the context of medical device capital equipment.
  • Work location: Pleasanton, CA
  • Travel: up to 20%
  • Full time employment
  • Proven track record of leading and delivering highly technical projects in a cross functional environment.
  • Experience working in a structured design process such as ISO9000 or FDA QSR and knowledge of regulatory approval process and requirements.
  • Working knowledge of Design Control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485 or ISO9001 and EN46001.
  • Excellent computer skills with specific skills in Microsoft Office and proficiency in SolidWorks.
  • Desirable: Experience working with capital equipment having field upgradable software.
  • Desirable: Experience with phased medical device product development process and performing design transfer.
  • Desirable: Experience designing, building, and implementing manufacturing fixtures and processing aids.
  • Compliance with relevant county, state, and Federal rules regarding vaccinations.

What We Offer

~2 min read
A competitive base salary range of $125,000 - $135,000 and variable incentive plan
Stock options – ownership and a stake in growing a mission-driven company
Employee benefits package that includes 401(k), healthcare insurance and paid vacation

At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:

  • Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
  • Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
  • Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of firstname.lastname@calyxoinc.com. If you receive a request for information from any other domain, please contact us directly at info@calyxoinc.com to verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

Location & Eligibility

Where is the job
Pleasanton, United States
On-site at the office
Who can apply
US
Listed under
United States

Listing Details

Posted
April 15, 2026
First seen
April 15, 2026
Last seen
May 6, 2026

Posting Health

Days active
21
Repost count
0
Trust Level
42%
Scored at
May 6, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust
Calyxo
Calyxo
greenhouse

Calyxo, Inc. is focused on improving kidney stone treatment through its innovative CVAC System, a revolutionary all-in-one solution for kidney stone management.

Employees
125
Founded
2016
View company profile
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CalyxoManufacturing Engineer – Capital - Pleasanton, CA$125k–$135k