Staff Process Development Engineer

Calyxo, Inc.; Pleasanton (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Calyxo, Inc., a leading medical device company, is seeking a Process Development Engineer to drive technical projects and enhance manufacturing processes. The ideal candidate will have a BS in Engineering and at least 10 years of experience in the medical device industry, ready to contribute to innovative kidney stone treatment solutions in a dynamic team environment.

Benefits

Competitive base salary

Stock options

401(k) benefits

Healthcare insurance

Paid vacation

Qualifications

• Minimum of 10 years of experience in medical device manufacturing.
• Experience with mechanical and electrical systems preferred.
• Knowledge of ISO9000 or FDA QSR processes.

Responsibilities

• Initiate and complete technical projects for process improvements.
• Design and develop manufacturing procedures and tooling.
• Train production personnel on new processes.

Skills

Project Management

Communication

Problem Solving

LEAN

Six Sigma

Education

BS in Engineering

Tools

SolidWorks

Microsoft Office

Job description

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.

In This Role, You Will:

• Initiate, own, and complete technical projects resulting in new/improved processes for Calyxo products.


• Effectively communicate project status, schedule baselines, schedule issues, project risks, and major decisions across all company disciplines.


• Work closely 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.


• Design and develop 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.


• Generate and modify high-quality manufacturing process documentation and ensure that processes and documentation follow established policies and procedures.


• Utilize 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.


• Write and execute process and equipment validations (IQ/OQ/PQ).


• Ensure product quality and support regulatory compliance.

Who You Will Report To:

• Manager, Process Development Engineering

Requirements:

• Education: BS in Engineering or a combination of relevant education and experience.


• Minimum of 10 years of experience supporting medical device manufacturing. Experience with both mechanical and electrical systems preferred.


• Work location: Pleasanton, CA


• Travel: 5%


• Full time employment


• The following skills are desired:
  
  
  
  • Experience with electronics/PCBA assembly, troubleshooting, and failure analysis.
  
  
  • Experience designing, building, and implementing manufacturing fixtures.
  
  
  • Experience with catheter manufacturing processes.
  
  
  
  


• Experience in leading 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.


• 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 a compensation plan as follows:

• Competitive base salary


• Stock options - ownership and a stake in growing a mission-driven company


• Employee benefits package that includes 401(k), healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics

Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Disclaimer:

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 [e-mail]. If you receive a request for information from any other domain, please contact us directly at [e-mail] 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.