Manufacturing Engineer - Capital - Pleasanton, CA

Calyxo

$125K — $135K *
Manufacturing & Automotive
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or relevant experience
  • 5+ years in medical device manufacturing
  • Experience with electronic components/assembly for medical equipment
  • Led technical projects in cross-functional environments
  • Familiar with ISO9000 or FDA QSR compliance
  • Proficient in SolidWorks and Microsoft Office
  • Desirable: Experience with capital equipment software updates

Responsibilities

  • Support projects for new/improved manufacturing processes for CVAC 2.0
  • Collaborate with R&D and Quality teams to optimize processes
  • Contribute to manufacturing procedures and tooling design
  • Provide production line support with troubleshooting and improvements
  • Train personnel during product/process transitions
  • Update manufacturing documentation and ensure compliance
  • Apply LEAN and Six Sigma for continuous improvement

Benefits

  • Join a knowledgeable and experienced team
  • Opportunity for career growth and ongoing learning
  • Diverse work environment with proven leaders
  • Participation in shaping company culture
  • Stock options for ownership and long-term investment
Full Job Description
Summary:

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.

In This Role, You Will:
  • 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.

Who You Will Report To:
  • Principal Manufacturing Engineer

Requirements:
  • 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:

At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.

We also offer an attractive compensation package, which includes:
  • 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

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