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Sr. Manufacturing Engineer

Intuitive
United Statesfull_timeVerifiedPosted 4 Feb 2025

About the role

Company Description

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.
As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible.
Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves.
Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential.
Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care.

Job Description

Primary Function of the Position

Contribute your technical manufacturing and equipment design skills to a dynamic team creating endoscopes, capital equipment, accessories, and precision instruments for minimally invasive robotic-assisted surgery.

The role requires effective participation in new product development teams, involves providing support for manufacturing lines, developing manufacturing equipment, and refining electro-mechanical components, assemblies, process documentation, tooling, and test methods. Additionally, it involves challenging product designs to improve efficacy, reliability, manufacturability, and cost for robotic surgical equipment.

Essential Job Duties

  • Create, maintain, and improve “low to high-volume” manufacturing lines, specifying and/or refining BOMs, workflow processes, manufacturing plan and detailed work instructions.
  • Apply engineering concepts to the optimization of equipment and procedures to achieve better maintainability, reliability, capacity, and availability of equipment.
  • Independently and proactively calculates and reviews trends for equipment performance
  • Diagnose equipment breakdowns to define and implement improvement strategies.
  • Perform installation, repair, and upkeep services for a variety of equipment either in the fields of mechanics and electronics.
  • Resolve emergency and unscheduled problems/repairs of equipment.
  • Design, document, procure, qualify, implement, and improve fixtures, tools, or equipment.
  • Responsible for creation and upkeep of equipment qualification approaches (IQ/OQ/PQ/DQ) including input from risk documentation and pFMEA
  • Responsible for the validation and qualification of manufacturing equipment and processes to production status leveraging standard qualification approaches (IQ/OQ/PQ/DQ)
  • Responsible for handling multiple priorities and projects as a matter of routine
  • Able to operate exclusively to develop innovative solutions and processes
  • Orchestrates approach to establish root cause and problem solving on complex issues
  • Demonstrate leadership through knowledge transfer, mentoring, and training of others
  • Conduct testing of software releases before deploying on manufacturing line
  • Identify and implement continuous improvement projects with respect to first pass yield, cycle time reduction, product reliability, capacity enhancement and cost reduction
  • Execute and mentor others in manufacturing process validations, process FMEAs and other elements associated with production Master Validation Plans
  • Maintain compliance with medical device quality system including corrective action closure and Change Order implementation
  • Conduct SAP transactions relevant to process or equipment operations.
  • Provide technician training and oversee specified manufacturing stations to ensure quality.
  • Contribute to the establishment of group and personal goals consistent with overall product development goals, including planning, priority setting, establishment of metrics, and effectively communicating progress
  • Specify, fit, and integrate new equipment and ensure it is working properly, along with required documentation
  • Proactively seeks better and improved technologies for improving production processes
  • Provide resource planning and

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Company

Intuitive

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