Sr. Engineer, Electrical

Gener8, LLC•San Jose, CA

8d•$104,408 - $139,211•Onsite

About The Position

In this role you will have the opportunity to work on the engineering team in San Jose, CA. This role involves working on current and next-generation designs of medical instruments. You will be part of a dedicated team, working in a dynamic environment. Open communication, empowerment, innovation, teamwork, and customer success are the foundations of the team.

Requirements

4+ years’ experience designing, testing, manufacturing or other engineering support and Medical device experience
Experience working with cross-functional teams
Experience owning and driving deliverables within a team and as an individual contributor in a fast-paced, changing environment
Proficient in collaborating with project stakeholders (client and internal), end-users, business partners, and technical team members
Strong organizational and follow-up skills, as well as attention to detail
Strong verbal and written communications with ability to effectively communicate to all levels of the organization
Distilling complex topics into easily digestible content, headlining key points
Design, modeling and simulation, physical prototyping
Circuit design aptitude – the ability to translate requirements into circuit designs/specifications
Modeling and simulation experience both in the circuit domain as well as free space
Proficiency with Comsol/Ansys/HFSS/CST or other similar packages, both in the context of creating new designs as well as debugging issues
Demonstrated initiative in going beyond assigned tasks on own agency
History of applying critical thinking to address design challenges
Ability to plan, execute, analyze, and document individual scientific studies
Ability to collect, organize, and analyze data using statistical methods
Bachelor’s degree in Electrical Engineering, Physics or equivalent experience.
Minimum 4 years work experience in Electrical Engineering.

Responsibilities

Contribute to a team committed to delivering the next generation of products
Drive the continued transformation of capabilities, equipment, and facilities
Conduct bench and preclinical studies supporting product development teams for concept feasibility and formal regulatory submission
Contribute to the continuous improvement of electronic designs
Draft test protocols and reports
Independently plan, coordinate, and execute activity in support of project goals
Conduct design reviews
Support development of risk management documentation
Gain an understanding of the quality and regulatory requirements, FDA and ISO regulations
Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
Perform other related duties and responsibilities, on occasion, as assigned