Principal/Sr. Principal Device Design Engineer

Alcon•Fort Worth, TX

1d•Onsite

About The Position

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Principal/Sr. Principal Device Design Engineer, you are responsible for designing and developing mechanical components or systems including: -Applying mechanical engineering principles to develop components and systems that involve movement (e.g., engines, vehicles, robots, prosthetic devices, energy conversion systems, machinery, etc.) -Supporting and participating in the design, test, modification, fabrication, and assembly of prototype mechanical components, systems, and assemblies -Collaborating with marketing and industrial design teams to develop components and systems that meet technical/functional specifications as well as manufacturing cost/efficiency requirements. This role is on-site in Fort Worth, Texas and a typical day would include: Responsible for supporting device engineering activities for ocular health related new products. He/she will support research & development in the area of novel ophthalmic devices (including novel packaging/ delivery devices) Hands on participation in or support the product development activities such as design development, prototyping/testing, pilot builds, verification & validation testing, risk assessment and production tooling validation. Applies statistical principles to communicate meaningful conclusions relevant to customer needs Applies knowledge of materials and manufacturing methods for medical devices Generate detailed fabrication drawings utilizing GD&T and tolerance analysis, appropriate product requirements and technical file documents and lead design reviews. Applies principles of engineering analysis to blend technical knowledge and manufacturing practices in providing solutions to complex engineering challenges. Develops requirements, leads design reviews, performance of verification and validation, production transfer and related documentation. Generates internal reports for communication with cross-functional members and management. Support all aspects of documentation. Verification Plans and Reports; and design control through ECN, and Windchill. Support existing device and ophthalmic packaging by addressing select product support requests and addressing questions on existing products. Ensures regulatory / statutory / legislative compliance for all project work.

Requirements

Bachelor’s Degree or Equivalent years of directly related experience (or high school +13 yrs; Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs)
The ability to fluently read, write, understand and communicate in English
5 Years of Relevant Experience

Nice To Haves

Experience in Medical Device Design and Development preferred.
Working Knowledge with FEA analysis is preferred
Proficiency with statistical analysis and software is preferred
Experience with evaluation of mechanical systems and assemblies.
Working knowledge and experience with fluidic systems.
Working knowledge and experience with electronics and electrical systems.
Ability to perform root cause analysis investigation
Knowledge of ISO, FDA, MDD and regulations applicable to the design and development of medical device/science/technology.
Proficiency in CAD. SolidWorks or Creo and related detailed drawings.
Working knowledge of plastic parts manufacturing processes like injection molding, blow molding, and 3D printing.
Strong technical writing capability in generating technical documentation
Ability to work under minimum oversight to identify and prioritize work activities as necessary to achieve project goals within set timelines.
Work efficiently and productively with other team members and external partners.
Adheres to Alcon's guidelines for appropriate workplace behaviors and attitudes.

Responsibilities

Applying mechanical engineering principles to develop components and systems that involve movement (e.g., engines, vehicles, robots, prosthetic devices, energy conversion systems, machinery, etc.)
Supporting and participating in the design, test, modification, fabrication, and assembly of prototype mechanical components, systems, and assemblies
Collaborating with marketing and industrial design teams to develop components and systems that meet technical/functional specifications as well as manufacturing cost/efficiency requirements
Responsible for supporting device engineering activities for ocular health related new products.
Support research & development in the area of novel ophthalmic devices (including novel packaging/ delivery devices)
Hands on participation in or support the product development activities such as design development, prototyping/testing, pilot builds, verification & validation testing, risk assessment and production tooling validation.
Applies statistical principles to communicate meaningful conclusions relevant to customer needs
Applies knowledge of materials and manufacturing methods for medical devices
Generate detailed fabrication drawings utilizing GD&T and tolerance analysis, appropriate product requirements and technical file documents and lead design reviews.
Applies principles of engineering analysis to blend technical knowledge and manufacturing practices in providing solutions to complex engineering challenges.
Develops requirements, leads design reviews, performance of verification and validation, production transfer and related documentation.
Generates internal reports for communication with cross-functional members and management.
Support all aspects of documentation. Verification Plans and Reports; and design control through ECN, and Windchill.
Support existing device and ophthalmic packaging by addressing select product support requests and addressing questions on existing products.
Ensures regulatory / statutory / legislative compliance for all project work.