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Sr Manager, Manufacturing Engineering

Job in Sunnyvale, Santa Clara County, California, 94087, USA
Listing for: Intuitive
Full Time position
Listed on 2026-03-01
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma, Process Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 194400 USD Yearly USD 194400.00 YEAR
Job Description & How to Apply Below
  • Ways of Working:
    Onsite - This job is fully onsite.
  • Employee Type:
    Employee
  • Min. Salary Region 1: 194400 USD
  • Global Job Level (HCM):
    Management 4, Sr Mgr (14)
  • Min. Salary Region 2: 165200 USD
Company Description

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive
. As a global leader in robotic-assisted surgery and minimally invasive care
, our technologies—like the da Vinci surgical system and Ion
—have transformed how care is delivered for millions of patients worldwide.

We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.

If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare
, you’ll find your purpose here.

Job Description

Primary Function of the Position

Contribute your technical manufacturing, leadership, and project management skills to a dynamic manufacturing engineering team creating precision instruments for minimally invasive robotic surgery. This key technical management role will guide and mentor a talented engineering team responsible for supporting instruments product launches by designing manufacturing lines and equipment, improving manufacturing processes, creating and maintaining all associated manufacturing documentation, dispositioning discrepant material, and maintaining compliance with our quality system.

Lead a team of Product Manufacturing Engineers, in collaboration with other organizations, to support

production of complex products with responsibilities including but not limited to:

  • Provide strategic and technical leadership to the Manufacturing Engineering organization.
  • Ensure the professional development of individual team members.
  • Establish group and individual objectives, priorities, and metrics.
  • Manage and allocate team resources over multiple projects. Provide and solicit resources to and from other teams as necessary.
  • Lead the Manufacturing Engineering team to launch mid-volume MP instruments products.
  • Ensure fulfillment of product development goals.
  • Create, maintain, and improve “mid-volume” manufacturing assembly lines, specifying and/or refining BOMs, workflow processes, manufacturing plan, and detailed work instructions.
  • Analyze instrument-manufacturing line from a risk perspective (PFMEA) to incorporate and validate critical tests used in manufacturing.
  • Specify, design, document, build and qualify the equipment necessary to perform each process step, while providing necessary manufacturing capacity.
  • Responsible for the validation and qualification of manufacturing equipment and processes leveraging standard qualification approaches (IQ/OQ/DQ/PQ).
  • Analyze the data from current Manufacturing Operations to review trends, opportunities for improvement and implement changes on a continuous basis
    • Ensure reliability and efficiency improvements of existing products
    • Provide technical support for failure analysis and root cause investigation of product failures.
  • Maintain compliance with medical device quality system including corrective action closure, discrepant material disposition and Engineering Change Order (ECO) implementation.
  • Work with Quality Engineering group to ensure that the team follows appropriate GMP, design history file (DHF), and device history record (DHR) guidelines per FDA requirements, and support design reviews in accordance with product development procedures.
Qualifications

Required Skills and Experience

  • Minimum of ten years’ engineering experience manufacturing complex electro-mechanical products.
  • Ability to motivate, mentor, and inspire a high-capacity technical team.
  • Experience developing products from early-stage concept to volume manufacturing.
  • Prior responsibility for validation of processes, equipment, and…
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