NPI Manufacturing Engineer

Join the Future of Robotic Biomanufacturing!

Multiply Labs is a robotics company on a mission to solve a significant bottleneck in modern medicine: the manufacturing of life-saving advanced biologics, from gene and cell therapies to antibodies and more.

Today, these therapies are produced through manual, labor-intensive processes. Costs are extremely high—often $500K–$2M per patient—limiting access to only a small fraction of those who need them.

As product complexity increases and the cost of failure and scientific labor rises, the industry is shifting toward automation. Robotics and AI are making automated biologics manufacturing feasible, reliable, and economically scalable.

We believe the future of biomanufacturing is robotic—closed, automated, and scalable—ensuring critical therapeutics are accessible to every patient who needs them.

Why This Matters

We don’t just build robots—we’re building the essential infrastructure for next generation biologics. Our technology enables biopharma companies to scale production without redesigning their science, reducing regulatory hurdles and lowering costs so these treatments can reach more patients.

The Stack & The Scale

The Mission: Build the world’s best robots to make life-saving therapies accessible to all.

The Technology: Advanced robotic orchestration, high-precision automation, cloud-integrated hardware-software systems, dextrous manipulation, and imitation learning.

The Location: Headquartered in San Francisco, CA.

The Backing: Supported by premier investors, including Casdin Capital, Lux Capital, and Y Combinator.

To learn more and to view a video of our robots in action, visit us at www.multiplylabs.com and follow us on LinkedIn .

About The Role We're looking for an NPI Engineer to own the transition of Multiply Labs’ Consumable products from R&D prototype to repeatable, in-house low-volume production — and eventually to contract manufacturing for product commercialization. This role suits someone with a well rounded background in medtech who is fluent in design transfer, creating rigorous documentation, and managing small-scale manufacturing operations.

Responsibilities

Lead design transfer from R&D prototypes to in-house pilot production: convert one-off prototype builds into controlled, repeatable processes a technician can execute independently

Design and build fixturing, select and implement new equipment on our pilot line

Develop, release, and maintain build documentation — work instructions, BOMs, LHRs, assembly drawings, inspection criteria, and test procedures. Train manufacturing team on new content.

Collaborate with R&D to drive DFX improvements

Coordinate with Quality to ensure compliance with industry standards and implement risk-based quality control for products

Schedule and coordinate builds with the onsite manufacturing team; troubleshoot issues in real time

Manage inventory and kitting with technician(s); partner with Supply Chain/Procurement Team on sourcing, part qualification, and vendor management

Track yield, first-pass quality, and build data; drive root cause analysis and implement improvements based on data

Own handoff to contract manufacturing in partnership with our Supply Chain team: create documentation packages, and manage the transition as volume or maturity outpaces internal capacity

Qualifications

Bachelor's in Mechanical or Biomedical Engineering (or equivalent experience)

1–4 years in manufacturing/NPI engineering, ideally in single-use medical device, diagnostics, or biopharma consumables manufacturing

Experience with design transfer, design controls, and documentation practices

Experience with process/equipment validation concepts (IQ/OQ/PQ) is a plus, even if not required in our current environment

Comfortable working hands-on with technicians, reading CAD/drawings, and working in a cleanroom manufacturing environment

Experience qualifying and working with contract manufacturers or suppliers

Statistical tools (SPC, capability studies) and risk management

Superb communication, collaboration, and problem-solving skills; comfortable in a fast-paced, startup environment

Exceptional organization skills and proven ability to work on multiple fast-paced projects simultaneously

Additional preferred experience:

Prior experience at a hardware startup or robotics company

Familiarity with biomanufacturing or lab automation

Experience working in regulated environments (e.g., GMP, FDA 21 CFR 820.30, ISO 13485)

Experience with the manufacturing of precision machine components (this role is primarily consumables based, but may have some overlap with capital equipment manufacturing)

Physical & Working Conditions

Ability to reach, stoop, crouch, and kneel, including entering and working inside a robotic cluster for maintenance, cleaning, or intervention

Ability to lift up to 25 lbs (equipment, parts, tools) and up to 5 lbs overhead

Manual dexterity to use hand tools, manage cabling, and perform mechanical adjustments

Work primarily in a manufacturing area adjacent to a lab; must follow strict safety protocols (e.g., BSL-2) and maintain situational awareness

Potential exposure to hazardous materials, including biological agents and cryogenics, while servicing equipment

Required use of PPE (cleanroom gowns, gloves, safety glasses, etc.) for extended periods

Standard work schedule with occasional evenings, weekends, or on-call support for critical issues or time-sensitive manufacturing needs

Perks & Benefits

Total Rewards & Life at Multiply Labs

Competitive Compensation: Salary range of $90,000 - $180,000 plus meaningful early-stage equity. We want our team to have a real stake in the future we’re building.

Premium Health: Premium Medical, Dental, and Vision plans with subsidies for child dependents.