Sr NPI Manufacturing Engineer

Intuitive•Sunnyvale, CA
•$132,900 - $225,000•Onsite

About The Position

We are seeking a collaborative and technically strong Manufacturing Process Engineer to support next-generation needles and accessories for advanced bronchoscopic instruments. In this role, you will lead the development, validation, and continuous improvement of manufacturing processes for precision flexible needles, catheters, and single-use accessory assemblies. You will partner closely with Design Engineering, Materials Engineering, Quality, and Supplier teams to ensure robust, scalable processes that deliver exceptional product performance and patient safety.

Requirements

  • Minimum of 8 years or Master's plus 6 years in manufacturing engineering, preferably in medical device, catheter, needle, or single-use disposable manufacturing environments
  • Experience with precision mechanical assemblies, polymer processing, and joining processes (e.g., laser welding, bonding, reflow).
  • Working knowledge of Six Sigma tools, Cpk, DOE, statistical process control
  • Root cause analysis experience (8D, Fishbone, DMAIC)
  • Familiarity with ALM/PLM systems for ECO and risk management
  • Basic coding proficiency in Python for data analysis or automation
  • Strong communication skills across technical and non-technical teams
  • Ability to manage multiple projects in a fast-paced NPI environment
  • Willingness to travel occasionally to suppliers or manufacturing sites
  • BS in Mechanical Engineering, Materials Engineering, Biomedical Engineering, or related field

Nice To Haves

  • Experience in medical device manufacturing (ISO 13485)
  • Familiarity with ISO 9001 and regulated product development environments
  • Hands-on experience with catheter, needle, or minimally invasive device assemblies, including packaging and sterilization validation
  • Experience with Agile and SAP systems or equivalent
  • Demonstrated success in experimental design and structured problem solving
  • Experience in Controlled Environment Rooms (CER)

Responsibilities

  • Develop, release, and validate scalable manufacturing processes for next-generation flexible needles, single-use and multi-use accessory assemblies.
  • Support development of joining and forming processes such as laser welding, adhesive bonding, tipping, grinding, crimping, swaging, polymer reflow, and more.
  • Define robust assembly and inspection methods for precision needle, catheter, and small-bore tubing subassemblies.
  • Ensure high-quality build and test practices, including tensile, pull, puncture, and dimensional testing, as well as packaging and sterilization compatibility.
  • Perform statistical analysis including Cpk, process capability analysis, DOE, ANOVA, regression analysis
  • Monitor yield trends and implement corrective actions to improve manufacturability and reliability.
  • Create and maintain pFMEAs and mitigate identified risks.
  • Collaborate with automation, equipment, and test engineering to improve automated test coverage and data traceability.
  • Partner with Mechanical and Materials Design Engineers on DFM/DFX reviews
  • Partner with Clinical and Human Factors teams to understand needle and accessory performance and usability needs
  • Partner with Supplier Engineering on tubing, extrusions, machined, molded, and packaging components
  • Support early NPI ramp to launch
  • Provide hands-on support to the production line during issue resolution and scale-up.
  • Lead root cause investigations involving needles and accessories.
  • Implement yield and cycle time improvements in needle and accessory assembly processes.
  • Develop and revise detailed manufacturing process instructions for processes.
  • Train technicians and manufacturing staff in new processes and quality standards.

Benefits

  • market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity
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