South San Francisco,, CA · Architecture/Engineering
Job Title: Staff Mechanical Engineer Location: On-site – South San Francisco, CA (relocation package available) Type: Full-Time FTE Salary range $90,000 - $200,000
The primary focus of this position will be to develop, test, and assemble critical engineering subsystems. As a Staff Mechanical Engineer, you will take ownership of a wide range of tasks pertaining to high-value internal projects - from requirements capture to novel concept research & development, to CAD design and component selection, to bring-up and testing of finished assemblies.
During this process, you will be required to provide in-depth analysis and help guide important decisions during design reviews and architecture discussions. You will create novel concepts through research and drive rapid feasibility studies with data collection.
This is a multidisciplinary role & this individual will interface across many parts of the company (with scientists, researchers, and engineers) to develop the best solutions possible. The successful candidate will be a resident expert in the areas of mechanical design, fluidic control, and highly automated instrument development. This is a hands-on position located onsite in South San Francisco, CA.
Responsibilities
Responsible for the design, development, and prototyping of mechanical components and consumables used in mechanical sub-systems & complex biotech instruments
Design and development of automated test fixtures to validate the reliability and robustness of novel components
Interface with systems & mechanical engineering teams to negotiate designs that meet product requirements & are feasible to manufacture economically
Conduct design reviews and present fresh ideas, new technologies, and creative solutions to design problems
Define subsystem architecture
Show proof of concept through rapid prototyping
Ability to extract design requirements from a broad spectrum of user needs
Identify potential design risks and provide a path to derisk/pivot rapidly
Work closely with the scientific team through the creation of verification /validation protocols (IQ, OQ, PQ) and successful execution, data generation, report and documentation
Create comprehensive work instructions and manufacturing SOPs as needed for finished designs
Requirements
BS or MS in Mechanical Engineering, Mechatronics Engineering, or equivalent experience
12+ years of extensive, hands-on experience in biotech automation, semiconductor, or similar industries
Excellent verbal, written, presentation, and interpersonal skills
Strong analytical and problem-solving skills
Prior experience with FDA regulations and ISO, cGMP, and QMS standards is a plus
Knowledge and/or hands-on experience with machine shop tools a plus
Knowledge of GD&T, as well as strong proficiency with SolidWorks
Creative, self-motivated, and flexible to work in a small company environment and assume a wide variety of tasks
Work history with several successful iterations of highly automated instrument design and development (biotech industry experience preferred)
Desire to be part of a rapidly evolving organization with compelling technology and take products and processes to the next level
Experience with Python, or high-level scripting software languages, a plus
Self-awareness, integrity, authenticity, and a growth mindset