Manager, Vision R&D Engineering
Intuitive

Sunnyvale, California

Posted in Manufacturing and Production


This job has expired.

Job Info


Company Description

Job Description

The Manager of Vision R&D Engineering will be responsible for leading a team of engineers who a) contribute towards the next generation vision product families focusing on endoscope cables across various product lines, b) devise engineering test methods for engineering product evaluations and characterization. This role is a key part of making data driven decisions to improve product designs prior to launch in addition to improving existing production released hardware. The role will be leading cross functional teams for development on current and new products.

Roles and Responsibilities:

This role has a 2-fold leadership function. This key technical management role will guide and mentor a talented R&D engineering organization responsible for not only owning and developing the next generation of electro-opto-mechanical cable product designs, but also devising robust engineering test methods for product evaluations and characterization for endoscopes and accessories. The team shall work closely with the electrical, optical, and other mechanical teams to collaboratively develop these novel cable designs. Additionally, this R&D Engineering team shall work collaboratively with the Supply Engineering teams and Manufacturing teams to transfer product improvements to volume manufacturing sites around the globe.

· Provide technical leadership to the Vision R&D Engineering organization

· Lead, and be responsible for novel product development work on endoscope cables, and test method development for endoscopes, and accessories

· Analyze the current endoscope cable performance, to identify opportunities for design improvements and implement changes

· Establish group and individual objectives, priorities, and metrics to:

· Ensure fulfillment of current customer demands

· Ensure progress towards Product Development goals

· Ensure reliability and efficiency improvements of existing products

· Ensure the professional development of individual team members

· Define product improvement strategies across all product platforms using vision cabling systems.

· Structure Bill of Materials (BOM's) including strategy for sub-assemblies

· Collaborate with the Endoscope design teams on multiple platforms, New Product Introduction (NPI) and Manufacturing teams to implement required manufacturing processes (Equipment, Manufacturing Instructions, Travelers, etc.)

· Collaborate with the Product Engineering team to proactively deliver improvements in endoscope cable performance and reliability

· Maintain compliance with medical device quality system, discrepant material disposition and Engineering Change Order (ECO) implementation.

· Lead cross functional team(s) in our Product Development Process (PDP) including: generating formal design documentation, review, and control (e.g. design reviews, ECOs, etc.), test method development, compliance with applicable local standards

· Work with cross functional development team (RA/QA/ME/NPV/CDE) to develop and manage project contracts, including; project plans, budgets, managing timeline, risks and issues to meet customer and business goals

· Supply chain strategy and management.

· Plan, budget and staff projects, tracking performance throughout.

· 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.

· Clearly define and motivate unmet needs and their context in the marketplace.

· Coach, develop and manage the engineering team through influential leadership, balancing the development objectives of the team with the needs of the organization.

Qualifications

Core Competencies, Skills and Experience Requirements:

· B.S. degree in Engineering discipline, M.S. preferred.

· Minimum of 8 years' of direct experience managing/mentoring engineers is preferred

· Minimum of 10 years' experience in design, manufacturing, or service environment for complex electro-mechanical products.

· Experience with medical cabling design and interface design is preferred.

· Track record of leading and developing sustainable teams.

· Knowledge of ISO requirements and GEP/GMP guidelines.

· Familiarity with sterilization processes and design guidelines for sterilization and reprocessing

· Familiarity with small part assembly and manufacture

· A passion for creating robust and reliable products

· An excitement to get to the bottom of challenging technical problems

· Proven ability to maintain schedule while bringing products from concept to manufacturing introduction.

· Strong mechanical engineering intuition

· Track record as a systems level architect and demonstrated ability to lead teams to realize the architectural vision

· Prior experience in medical device manufacturing/field data analytics is a plus

· Ability to motivate, mentor, and inspire a high capacity technical team.

· Prior responsibility for validation of products is a plus.

· Experience with data analysis and scripting tools, Matlab, etc. preferred

· Knowledge of a wide range of manufacturing processes, such as machining, extrusions, overmolding, injection molding, MIM, laser welding, soldering, crimping, and other forms of joinery.

· Strong quantitative process development skills including (d)FMEA, (p)FMEA, tolerance analysis, DoE, SPC, GR&R, and CpK.

· Familiarity with mechanical CAD software (Solidworks).

· Excellent organizational skills; Able to manage multiple fast-paced projects simultaneously.

· Prior experience with Agile Change Control and SAP is a plus.

· Ability to communicate effectively and professionally across a range of technical disciplines with a broad slate of stakeholders, including management, peers, customers, and suppliers.

· Prior experience with the Design Control processes for medical devices and clinical application of surgical instruments is a plus

· Experience in an ISO 13485, ISO 9001, or medical device manufacturing environment preferred

Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.

Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Shift : Day

Travel : 10% of the time

Travel Requirements:10% of the time Shift:Day


This job has expired.

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