Engineer 2, Sustaining, R&D

Teleflex

Sustaining R&D Engineer focusing on existing Anesthesia and Emergency medicine products. Managing projects and providing engineering solutions at Teleflex.

Posted 7/25/2026full-timeMorrisville • North Carolina • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in sustaining engineering projects for Anesthesia and Emergency medicine products, with a strong focus on product design, development, and compliance within the medical device industry. Proficient in managing multiple projects, conducting risk analysis, and preparing formal documentation while ensuring adherence to regulatory standards.

Highest-signal resume keywords

Bachelor's Degree In Engineering3-5 Years Experience In Medical Device DevelopmentSolidWorks CADD ProficiencyISO And ASTM Testing ExperienceStrong Written And Verbal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Product DesignChange ManagementRisk AnalysisValidation Protocol DevelopmentInjection MoldingPlastic ExtrusionPlastic Part Assembly

Soft Skills

Attention To Detail

Tools & Technologies

Microsoft Office SuiteSolidWorks

Industry Keywords

Medical Device IndustryFDAMDDMDRISO Standards

Tech Stack

Tools & technologies

Assembly

About the role

Key responsibilities & impact

Responsible for the sustaining engineering projects of Anesthesia and Emergency medicine products.
Organizing and managing multiple projects and ensuring timely completion.
Provide creative solutions to technical issues or modifying/improving products.
Acts as product technology group owner/subject matter expert for assigned product lines.
Coordinates product design and development process with engineering, quality, regulatory, and marketing departments.
Serve as an R&D technical lead representative in transfer and integration core teams.
Prepare formal documentation of product designs, change management, risk analysis, product requirements, and specifications.
Conducts research on projects associated with design and/or design modifications of medical devices.
Develop and coordinate execution of protocols for validations of new or modified devices or components.

Requirements

What you’ll need

Bachelor’s Degree in Engineering
Minimum 3-5 years of work experience in the development of devices within the medical device industry.
Experience in SolidWorks CADD (design/drafting) program preferred
Microsoft Office Suite (Project, Word, Excel) required
Injection molding, plastic extrusion, plastic part assembly experience a plus
Experience working within the medical device-related industry requirements (FDA, MDD, MDR, ISO Standards, etc)
Testing experience using ISO and ASTM testing methods for medical devices and general plastic components preferred
Strong written and verbal communication skills and attention to detail.
Speak and write English fluently.

Benefits

Comp & perks

Up to 10% travel
Equal opportunity employer