As a Senior Manufacturing Process Engineer, you will drive the creation and validation of manufacturing processes for a next-generation active implantable brain-computer interface device. Your work will bridge product design and production, ensuring that specifications are accurately translated into reliable, scalable processes across suppliers and internal teams.
What You'll Do
You will serve as the technical liaison between Echo and its suppliers, ensuring components and assemblies meet design intent and regulatory standards. You'll collaborate closely with product development to influence design for manufacturability and support the transfer of designs into production. This includes developing detailed documentation that aligns supplier processes with internal engineering requirements.
You will lead risk assessments such as Process FMEAs, support validation protocols, and conduct failure analysis when needed. A key part of your role is to refine supply chain processes to increase efficiency and reduce waste, while maintaining strict adherence to quality systems. You will also resolve non-conformances and lead corrective actions with suppliers, ensuring alignment with FDA and EU regulations.
Requirements
- BS in an engineering discipline or equivalent practical experience
- Minimum of 10 years in medical device manufacturing, ideally within startups focused on electro-mechanical systems
- Direct experience with active implantable devices, including implants, leads, and external components
- Proven background in molding, laser welding, cleanroom assembly, packaging, labeling, and sterilization processes
- Hands-on expertise in PCB fabrication, PCA assembly, microelectronics, flip chip, in-circuit test (ICT), and functional testing
- Experience with manufacturing automation and test systems
- Strong track record in process validation execution and documentation
- Proficiency with Solidworks, LabVIEW, and manufacturing/test automation software
- Ability to navigate and reconcile differences between supplier capabilities and internal quality system requirements
- Deep understanding of FDA and EU regulatory expectations for medical device manufacturing
Benefits
- Engagement in transformative medical technology with direct patient impact
- Competitive salary and stock options
- Comprehensive health, dental, and vision coverage
- 401(k) plan with company matching
- Opportunities for professional growth in an early-stage, decision-driven environment
Work Mode
This is an onsite role based in Minnesota, with frequent domestic and international travel required to support supplier development and manufacturing scale-up.
Company Culture
You’ll join a culture that values ownership, collaboration, and continuous improvement. With cross-functional teams working in close alignment, your contributions will directly influence product success. The environment supports learning, innovation, and personal development, with a shared commitment to advancing neurotechnology for patient benefit.
Equal Opportunity Employer
We are an Equal Opportunity Employer and welcome individuals of all backgrounds. Diversity is central to our mission, and we are dedicated to fostering an inclusive workplace where every voice matters.
