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R&D Engineer Tracheostomy

Teleflex -
Athlone, County Westmeath

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Job details

18 hours ago

Qualifications

Microsoft Office
Minitab
Analysis skills
Bachelor's degree
SolidWorks
Communication skills

Full job description

Date: Jun 15, 2026

Location: Athlone, L, IE

Company: Teleflex

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Position Summary

Lead the delivery of projects to maintain business continuity in areas such as new product introduction and sustaining engineering of existing products in the Tracheostomy portfolio.

Principal Responsibilities

Work related to products and components may include efforts in all technical phases of product and process development, including design and development planning and execution, requirements definition, root cause analysis, verification/validation and manufacturing aspects using companies design control policies, as well internal business processes.
Meet project objectives, milestones, and target dates. Update and review project progress on an as-required basis by supervisor.
Lead engineering efforts to develop components, specifications and processes with input from technical experts, clinicians, marketing and manufacturing while adhering to the design control process.
Lead projects in the redesign or replacement of existing components/assemblies and processes to improve quality, utilize automated production techniques, optimize process capabilities, and produce better products in a more cost-effective manner.
Perform product testing, create models and prototypes to prove out new designs and changes to existing designs.
Coordinate both virtual and in-person interactions with manufacturing sites, suppliers, and cross-functional teams (Engineering, Sourcing, Quality, and Regulatory Affairs) to deliver projects.
Participate in Front End Innovation (FEI) activities for the New Product Development pipeline, including market research, concept generation and development.
Interface with suppliers to obtain quotations, purchase components, and debug problems with production parts.
Lead and participate in design and technical phase reviews.
Support regulatory submissions, CAPAs, NCs and clinical trials as required.
Adhere to and ensure the compliance of Companies Code of Conduct, all Company policies, rules, procedures and housekeeping standards.

Education / Experience Requirements

Bachelor of Science in Mechanical or Biomedical Engineering preferred; other technical disciplines will be considered.
1-3 years previous experience in related field (e.g. medical device manufacturing and assembly, disposables manufacturing processes, plastics, automation.
Strong analytical, technical and problem-solving skills.
SolidWorks or equivalent modelling system proficiency and technical documentation essential.
Previous experience in design of medical devices preferred.
Effective verbal and written communication skills.
Team player with good interpersonal skills.
Proficient in Microsoft Office Suite; familiar with statistical analysis (Minitab) applications.

Specialized Skills / Other Requirements

Self-motivated, high energy, positive attitude individual with the initiative and drive for timely completion of goals.
The ideal candidate will display excellent multi-tasking, analytical, communication and prioritisation skills.

TRAVEL REQUIRED: <10 %.

WORKING ENVIRONMENT: Office/Professional (Hybrid)

#LI-PD1

Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.
If you require accommodation and support to apply for a position, please contact us at [email protected].
Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

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