Senior NPI Process Development Engineer

Neptune Medical; Burlingame (CA); On-site; USD 140,000 - 175,000; Full time

Benefits offered by this job

Equity opportunities

401(K) matching

Comprehensive benefits

Job summary

A medical device startup is seeking a Senior NPI Process Development Engineer to develop and transfer product manufacturing processes. This position demands cross-functional collaboration to enhance product development and reduce manufacturing costs. The ideal candidate has a degree in engineering, extensive experience in medical device manufacturing, and a passion for innovation. The startup environment promises a dynamic and exciting work atmosphere, along with competitive salary and benefits.

Qualifications

• 4+ years of work experience in medical device industry.
• Experience in generating manufacturing documentation.
• Solid understanding of FDA regulations and GMP.

Responsibilities

• Engage in cross-functional collaboration for product development.
• Prototype manufacturing processes using various tools.
• Ensure compliance to quality management policies.

Skills

Cross functional teamwork

Process validation

CAD modeling

Successful engineering projects

Strong desire to succeed

Education

B.S. or M.S. in Mechanical or Related Engineering

Tools

SolidWorks

Job description

Neptune Medical is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Triton Robotic Endoscopy will disrupt flexible endoscopy and set a new standard in outcomes for decades to come.

Title

Senior NPI Process Development Engineer

Position Summary

The Senior NPI Process Development Engineer will focus on further developing our product and then transferring it into a manufacturing setting. The successful candidate will possess a passion for medical device engineering and a record of successful process, tooling and equipment design. This role will engage in cross-functional collaboration to accelerate the product development process, reduce cost of goods, and enable more complex designs through manufacturing improvements.

The ideal candidate will act with passion and intensity in a medical device start-up that is fast paced and collaborative and will display the ability to perform to the requirements outlined below. For the right person, this position will be a tremendously exciting and career-defining opportunity, making core contributions to a genuinely new type of medical robotic platform.

Roles and Responsibilities

• Work with product development to design and prototype novel manufacturing processes and equipment
• Develop new processes to manufacture our products to meet device performance and cost targets.
• Design and prototype novel manufacturing equipment and fixturing
• Create and maintain necessary Manufacturing Process Instructions (MPI’s), test methods, product drawings, and component specifications
• Upgrade our manufacturing processes to ensure proper DFM and maximum scalability of our medical devices
• Initiate and implement programs to continuously improve quality, cost and cycle time
• Prototype fixtures using 3-D printers, lathe, drill press, band saw, etc.
• Provide technical support and perform failure analysis for non-conforming components, assemblies, and process defects
• Build the assembly line for our clinical launches
• Specify, support and maintain the proper CER space to manufacture our medical devices under defined environmental quality controls.
• Manage the flow of WIP through Lean practices including Kanban and 5S.
• Maintain relationships with key vendors and suppliers and support supplier validations and supplier management best practices.
• Emphasize quality and utilize a risk-driven approach to ensure compliance to risk management policies and practices and ensure GMP.
• Support company goals and objectives, policies and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic regulations including Cal FDB, OSHA and Cal-OSHA.

Required Qualifications

• B.S. or M.S. in Mechanical or Related Engineering
• 4+ years of work experience
• Demonstrated experience working with cross functional teams.
• Proven track record of generating and managing manufacturing documentation from concept to commercialization for medical device product (MPIs, LHRs, BOM, flowcharts, etc.)
• Capable with CAD modeling, engineering drawing generation, DFM, tolerance analysis and tooling design
• Possess knowledge of process validation, GMP, and state-of-the-art manufacturing processes
• A driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.
• Solid understanding of design controls
• Demonstrated success developing catheter manufacturing processes including braiding, coil winding, extruding, lamination, adhesive joining, die bonding, and laser welding.

Preferred Qualifications

• Experience with catheter or similar manufacturing (lamination, bonding, dip coating, ultrasonic welding, etc)
• Experience with disposables/consumables
• Experience managing lab technicians and assemblers.
• Developed products from invention to market release.
• Experience in a start-up environment.
• Proficient with SolidWorks.
• Experience creating and managing schedules, budgets, and plans.
• Experience with packaging and shipping validations

Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART station.

The starting base salary for this role is between $140,000 and $175,000 depending on experience. The role may also be eligible for equity, benefits and 401(K) with matching.

Neptune Medical provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.