A better night’s sleep is just around the corner.


Want to make a difference in this world by trying to solve one of the most common sleep problems in the world? Are you passionate about helping individuals’ live better lives who suffer from sleep disorders? Do you want to work with innovative products and in a creative teamwork environment? Cerêve has developed an innovative, new-to-market device to help individuals with insomnia. With recent US FDA clearance, we are currently seeking highly motivated and skilled, creative professionals to join our growing team. With millions of people suffering from insomnia, you would be a part of a talented group of individuals who are passionate about bringing new technology and products to market that help individuals with chronic sleep disorders live better and more productive lives.


Cerêve has an immediate need for a full time Lead Mechanical Engineer that is innovative and willing to stretch the bounds of creativity. In a dynamic and energizing environment, the Lead Mechanical Engineer is responsible for providing engineering expertise in all aspects of new product development, including the creation, design, and development for all Cerêve products. Candidate must have strong analytical, statistical, database and spreadsheet skills with excellent written and oral communication skills, a Can-Do-Attitude and a willingness to learn. The position requires limited domestic travel (5%).

Primary Responsibility:

-Responsible for participating in all aspects of new product development

-Interact with the leadership team to ensure all key product requirements are achieved

-Brainstorm and develop new technologies in support of the overall company product strategy

-Lead phases of new product development through the stage-gate process

-Participate in product development strategies


-Minimum of 10 years of experience in electro-mechanical medical product device development

-Proven track record in all aspects of product design from concept, detailed design, and transfer to manufacturing for high volume production

-Working knowledge of FDA Requirements within a medical product development environment

-Product team leadership experience

-Industrial design experience

-Highly Proficient in 3D CAD (SolidWorks preferred)

-Experience in Fusion 360

-Experience in FEM analysis

-Thermodynamic analysis

-Knowledgeable and experienced in plastic part design and tooling

-Proficiency in MS Office Products (Word, Excel, PowerPoint)

Educational Requirements:

-B.S. in Mechanical Engineering

-M.S. in Mechanical Engineering, preferred

-Training in FDA design control processes a plus


A comprehensive compensation package including a competitive base salary, medical benefits and 401k with company match.

Cerêve is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, sex, national origin, sexual orientation, gender identity, age, status as a protected veteran, status as a qualified individual with a disability, or any other protected class status.