Second Sight offers a fast paced environment that challenges employees to be both productive and creative. Team members are encouraged to explore new solutions to existing problems while, at the same time, remaining focused on the objective of restoring vision to the blind. Second Sight offers competitive wages and benefits. If this sounds like the right opportunity for you then please send your resume to: HR@secondsight.com
Second Sight Medical Products, Inc. Human Resources
12744 San Fernando Road, Suite 400
Sylmar, CA 91342
Principal Mechanical Engineer - USA
Researches, plans, designs and documents mechanical and electromechanical parts and assemblies. Coordinates and carries out activities involved in documentation, production, testing, operation and repair of mechanical or electromechanical parts and assemblies. Applies advanced theoretical analysis to the optimization of such assemblies. You will be considered a specialist in the field. May lead project modules and may have supervisory responsibilities.
Senior Mechanical Engineer - USA
As a member of Implant R&D team the senior mechanical engineer will be a key player in the design and development implants for giving sight to the blind, as well as for fixtures and hardware for manufacturing of the same. We are looking for someone with experience working on a development team to iterate novel implant designs based on pre-clinical and clinical trials. Preferably medium-sized company experience with a mature product development system and a medium volume product (1000’s per year). DBS or cochlear implant product realization experience would be very beneficial. You will be instrumental in the design, verification, and validation of the Orion II Implant.
Quality System Records Associate (Temp, 3-6 mos.) - USA
Reviews and maintains DHR Traveler/ Traveler files of all the Quality System Records that make up the Device History Records of medical devices manufactured by SSMP. Works autonomously to collect, review, oversee correction of, and file these records. Maintain the Records room by scanning and filing documents/records, boxing up old records for offsite management. Help with other quality systems in record management.
Electrical Engineer II - USA
Researches and develops systems, designs circuits, and tests electrical components, equipment, and systems.
Electrical Engineer - ASIC Layout - USA
This position will play a key role in the ASIC group of the Implant R&D department as the main layout engineer. He/she will work with ASIC circuit design engineers on architectural design and floor planning, and carry out most of the chip circuit layout work to ensure timely submission for fabrication of chip designs in various development phases of ASIC for visual prosthesis. Additionally, this position is responsible for PCB layout for chip testing circuits, and plays a supporting role in chip testing.
Senior Software Engineer - USA
Senior full stack software developer with design and development experience using the latest web tools and technologies
Software Engineer - Research - USA
Develops and supports software for the Scientific Research department (i.e., psychophysics experiment scripts, clinical and analysis software applications) primarily in MATLAB.
Publications Specialist / Medical Writer - USA
Writes and submits Second Sight driven scientific articles for publication in peer-reviewed journals; writes and reviews conference abstracts; coordinates publications with/for outside investigators; and assists with internal report writing and grant submissions.
Senior Quality Engineer - USA
Develops, implements and maintains quality engineering methodologies, systems and practices which meet Second Sight quality and regulatory requirements. Provide quality engineering support in the design, development, manufacture and servicing of SSMP products to ensure that the products conform to established specifications and consistently meet or exceed the requirements of our customer and patients.
Senior Test Development Engineer - USA
Responsibilities include, but are not limited to, the development and support of manufacturing test systems (both hardware and software) for implantable medical products. Analyses production failures and takes corrective action.
Technical Writer, R&D - USA
Responsible for producing technical documentation such as engineering drawings, manufacturing instructions, travelers, protocols, and reports.
Senior Clinical Research Associate - USA
Responsible for performing monitoring of clinical trial sites (including site initiation, interim monitoring and study close-out), managing adverse event data, coordinating safety oversight activities, preparing adverse event reports to regulatory agencies, and interfacing with cross-functional departments (scientific affairs, R&D, regulatory, quality, finance/contracts) to ensure priority studies are executed according to timelines and deliverables.
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