Principal Engineer at Katalyst Healthcares Life Sciences
Round Lake, IL 60073, USA -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

0.0

Posted On

04 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Mechanical or Industrial Engineering

Description

Roles & Responsibilities:

  • With minimal guidance, the principal engineer schedules, interfacing with development groups and technical support groups.
  • The principal R&D engineer devises new approaches to complex problems through adaptations and modifications of standard technical principles.
  • The principal R&D engineer can prioritize multiple tasks.
  • The principal R&D engineer supervises / coordinates a Snr Engineer / Engineer and / or coordinator on assigned work.
  • The Principal R&D Engineer shall ensure that the right choices are being made with regards to material choice, overall set design and supplier selection within the Baxter operation.
  • The Principal R&D Engineer shall be knowledgeable of various manufacturing processes such as: assembly, extrusion and moulding.
  • The Principal R&D Engineer shall work towards meeting the intended use of the product in the various countries of sales, as applicable to the project s/he is leading.
  • The Principal R&D Engineer shall work towards developing/sustaining a product in accordance with Baxter’s defined Quality and Regulatory standards.
  • The Principal R&D Engineer shall be responsible for finalizing any reports/presentations related to his projects and any other necessary reports as the need arises.
  • The Principal R&D Engineer will also be responsible for the assignment of project activities within his/her project team, to meet committed milestones and project objectives.
  • Design Verification and Validation are to be carried out in accordance with ISO Standards, CE Norms, FDA, country specific norms and Baxter’s Quality Manual.
  • Design Verification Testing is to be planned/executed based upon knowledge of materials, fluid dynamics and correct usage/applicability of available equipment.
  • The principal engineer should be able to work with the Project Management Office (PMO), to plan out resources, budget, timelines throughout the project development lifecycle.
  • The principal engineer should be able to present the work achieved by his/her team to different stakeholders (as applicable).
  • The principal engineer should design with manufacturability in mind; leading his/her team through various development activities that would eventually allow a smooth design transfer to manufacturing.
  • Bachelor of Engineering (type not specific), 5-8yrs of experience with focus areas around leading and/or managing technical projects. Candidate should have experience with disposable medical devices (e.g. IV sets), manufacturing processes, and product development.
Responsibilities
  • With minimal guidance, the principal engineer schedules, interfacing with development groups and technical support groups.
  • The principal R&D engineer devises new approaches to complex problems through adaptations and modifications of standard technical principles.
  • The principal R&D engineer can prioritize multiple tasks.
  • The principal R&D engineer supervises / coordinates a Snr Engineer / Engineer and / or coordinator on assigned work.
  • The Principal R&D Engineer shall ensure that the right choices are being made with regards to material choice, overall set design and supplier selection within the Baxter operation.
  • The Principal R&D Engineer shall be knowledgeable of various manufacturing processes such as: assembly, extrusion and moulding.
  • The Principal R&D Engineer shall work towards meeting the intended use of the product in the various countries of sales, as applicable to the project s/he is leading.
  • The Principal R&D Engineer shall work towards developing/sustaining a product in accordance with Baxter’s defined Quality and Regulatory standards.
  • The Principal R&D Engineer shall be responsible for finalizing any reports/presentations related to his projects and any other necessary reports as the need arises.
  • The Principal R&D Engineer will also be responsible for the assignment of project activities within his/her project team, to meet committed milestones and project objectives.
  • Design Verification and Validation are to be carried out in accordance with ISO Standards, CE Norms, FDA, country specific norms and Baxter’s Quality Manual.
  • Design Verification Testing is to be planned/executed based upon knowledge of materials, fluid dynamics and correct usage/applicability of available equipment.
  • The principal engineer should be able to work with the Project Management Office (PMO), to plan out resources, budget, timelines throughout the project development lifecycle.
  • The principal engineer should be able to present the work achieved by his/her team to different stakeholders (as applicable).
  • The principal engineer should design with manufacturability in mind; leading his/her team through various development activities that would eventually allow a smooth design transfer to manufacturing.
  • Bachelor of Engineering (type not specific), 5-8yrs of experience with focus areas around leading and/or managing technical projects. Candidate should have experience with disposable medical devices (e.g. IV sets), manufacturing processes, and product development
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