Expected Travel: Up to 10%Requisition ID: 13589
About Teleflex IncorporatedAs 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, Rusch, 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.
Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow, Arrow, EZ-IO, and QuikClot brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.Position Summary The Sr. Design Engineer leads end-to-end development of advanced vascular access devices from early concept through commercialization and design transfer. This role integrates clinical insight, engineering rigor, and regulatory compliance to deliver innovative, manufacturable, and high-quality products. Operating within a matrixed organization, the Sr. Design Engineer partners with Technical Experts and Project Managers to ensure alignment to business objectives, timelines, and portfolio strategy while serving as a technical leader across disciplines.Principal Responsibilities Concept Developmento Translate clinical needs, market insights, and user feedback into clear user needs and design inputso Lead concept generation, feasibility studies, and early risk reduction activitieso Develop and evaluate innovative design concepts using engineering fundamentals and simulationo Conduct clinical observations and collaborate with clinicians to refine use cases and requirementso Lead early-stage DFMEA, UFMEA, and feasibility testing to guide design direction Design and Developmento Develop detailed design and development plans, identifying deliverables, gaps, and contingencies.o Lead detailed design of complex systems including mechanical, fluid, and material interactions including establishment of associated transfer functionso Develop CAD models, simulations, and engineering analyses to optimize performanceo Provide material selection expertise including polymers and metals, with sterilization compatibility.o Drive design for manufacturability, sterilization compatibility, and reliabilityo Own requirements traceability from user needs through design outputs; ensuring audit readiness and manufacturability.o Lead usability engineering activities and human factors integrationo Guide subsystem integration and system-level architecture decisions Verification, Validation & Complianceo Lead cross-functional teams in execution of robust design verification strategies.o Develop and execute design verification and validation strategies aligned with regulatory expectationso Own documentation of test methods and lead test method validation studies.o Ensure compliance with FDA and Teleflex design controls, ISO 13485, and ISO 14971o Author and review DHF documentation ensuring audit readinesso Support regulatory submissions including 510(k) and PMAo Lead risk management activities and ensure mitigation effectiveness Design Transfer & Manufacturingo Collaborate with manufacturing to ensure robust design transfer and scalabilityo Support process development and validation activities (IQ/OQ/PQ)o Ensure alignment between design intent and manufacturing capabilityo Participate in PFMEA and support production readiness and pilot buildso Drive resolution of design-related issues during transfer and launch Comply with Teleflex's Code of Ethics, all company policies, rules, procedures and housekeeping standards.
BEHAVIORAL COMPETENCIES Systems thinking and ability to integrate cross-disciplinary inputs Advanced problem-solving and root cause analysis Strong understanding of design controls and regulatory compliance Ability to translate ambiguous clinical needs into structured engineering requirements Technical leadership and cross-functional influence Risk-based decision making and prioritization Effective communication with technical and non-technical stakeholders Adaptability and ownership in a fast-paced development environmentEducation / Experience Requirements Bachelor of Science - Engineering or equivalent technical discipline Preferred: Master of Science - Engineering or equivalent technical discipline Minimum of 10 years of previous experience in a related field (e.g., medical device design and manufacturing, or similar regulated industry, plastic processing, injection molding).Specialized Skills / Other Requirements Technical Knowledge:Deep expertise in mechanical systems, fluid dynamics, and material properties as applied to vascular access and interventional devices, with the ability to apply first-principles engineering to develop and evaluate early-stage design concepts Ability to translate clinical workflows, user needs, and market insights into structured engineering requirements and design inputs, enabling development of innovative, patient-centric solutions Advanced capability in concept generation, feasibility assessment, and simulation-driven design, including development of analytical and computational models to evaluate performance, usability, and risk during early design phasesStrong application of Design for Manufacturability (DFM), Design for Assembly (DFA), and usability/ergonomic principles from concept through development to ensure scalable and robust product designsDemonstrated expertise in early-stage risk identification and mitigation, including application of DFMEA, UFMEA, and hazard analysis to guide concept selection and design refinementStrong command of verification and validation methodologies, with the ability to define testable design inputs and ensure traceability from concept through validation in alignment with ISO 14971 risk management principlesAbility to design and interpret advanced statistical analyses (e.g., DOE, tolerance analysis, feasibility data interpretation) to support concept down-selection, design optimization, and performance characterization
Regulatory and Compliance:In-depth knowledge and application of design control processes and global regulatory requirements (e.g., ISO 13485, FDA 21 CFR 820, EU MDR) in medical device developmentLeads design verification and validation activities, ensuring alignment with regulatory expectations, risk management, and usability engineering principlesOwns and drives change control activities, including ECOs, CAPA, and design changes, ensuring compliance and traceability across the DHF
Process Development and Manufacturing Support:Leads process development and validation activities, including defining and supporting IQ, OQ, and PQ strategies in collaboration with manufacturing and quality teamsDrives PFMEA and risk assessment activities, ensuring alignment between design intent and manufacturing capabilityApplies deep understanding of material behavior and manufacturing processes to optimize product performance, consistency, and yieldProject Management and Collaboration:Authors and reviews complex technical documentation, including design history files (DHF), verification protocols/reports, and regulatory submissionsLeads cross-functional collaboration across R D, Quality, Regulatory, Manufacturing, and Clinical teams, influencing decisions and driving alignmentCommunicates complex technical concepts effectively to diverse audiences, including leadership and external stakeholdersDemonstrates advanced analytical thinking and structured problem-solving, leading root cause investigations and implementing robust solutionsExhibits strong leadership, collaboration, and mentoring capabilities within a matrixed organizationHighly proficient in engineering tools, data analysis platforms, and design/simulation softwareDemonstrated expertise in polymer component design and catheter-based systems, including application to vascular access or interventional devices
Self-motivated, high-energy, positive attitude individual with the initiative and drive for timely completion ofgoals. Able to travel domestically and internationally.
#LI-DR1
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 Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: ... or .... Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rusch, 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.
About Teleflex IncorporatedAs 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, Rusch, 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.
Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow, Arrow, EZ-IO, and QuikClot brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.Position Summary The Sr. Design Engineer leads end-to-end development of advanced vascular access devices from early concept through commercialization and design transfer. This role integrates clinical insight, engineering rigor, and regulatory compliance to deliver innovative, manufacturable, and high-quality products. Operating within a matrixed organization, the Sr. Design Engineer partners with Technical Experts and Project Managers to ensure alignment to business objectives, timelines, and portfolio strategy while serving as a technical leader across disciplines.Principal Responsibilities Concept Developmento Translate clinical needs, market insights, and user feedback into clear user needs and design inputso Lead concept generation, feasibility studies, and early risk reduction activitieso Develop and evaluate innovative design concepts using engineering fundamentals and simulationo Conduct clinical observations and collaborate with clinicians to refine use cases and requirementso Lead early-stage DFMEA, UFMEA, and feasibility testing to guide design direction Design and Developmento Develop detailed design and development plans, identifying deliverables, gaps, and contingencies.o Lead detailed design of complex systems including mechanical, fluid, and material interactions including establishment of associated transfer functionso Develop CAD models, simulations, and engineering analyses to optimize performanceo Provide material selection expertise including polymers and metals, with sterilization compatibility.o Drive design for manufacturability, sterilization compatibility, and reliabilityo Own requirements traceability from user needs through design outputs; ensuring audit readiness and manufacturability.o Lead usability engineering activities and human factors integrationo Guide subsystem integration and system-level architecture decisions Verification, Validation & Complianceo Lead cross-functional teams in execution of robust design verification strategies.o Develop and execute design verification and validation strategies aligned with regulatory expectationso Own documentation of test methods and lead test method validation studies.o Ensure compliance with FDA and Teleflex design controls, ISO 13485, and ISO 14971o Author and review DHF documentation ensuring audit readinesso Support regulatory submissions including 510(k) and PMAo Lead risk management activities and ensure mitigation effectiveness Design Transfer & Manufacturingo Collaborate with manufacturing to ensure robust design transfer and scalabilityo Support process development and validation activities (IQ/OQ/PQ)o Ensure alignment between design intent and manufacturing capabilityo Participate in PFMEA and support production readiness and pilot buildso Drive resolution of design-related issues during transfer and launch Comply with Teleflex's Code of Ethics, all company policies, rules, procedures and housekeeping standards.
BEHAVIORAL COMPETENCIES Systems thinking and ability to integrate cross-disciplinary inputs Advanced problem-solving and root cause analysis Strong understanding of design controls and regulatory compliance Ability to translate ambiguous clinical needs into structured engineering requirements Technical leadership and cross-functional influence Risk-based decision making and prioritization Effective communication with technical and non-technical stakeholders Adaptability and ownership in a fast-paced development environmentEducation / Experience Requirements Bachelor of Science - Engineering or equivalent technical discipline Preferred: Master of Science - Engineering or equivalent technical discipline Minimum of 10 years of previous experience in a related field (e.g., medical device design and manufacturing, or similar regulated industry, plastic processing, injection molding).Specialized Skills / Other Requirements Technical Knowledge:Deep expertise in mechanical systems, fluid dynamics, and material properties as applied to vascular access and interventional devices, with the ability to apply first-principles engineering to develop and evaluate early-stage design concepts Ability to translate clinical workflows, user needs, and market insights into structured engineering requirements and design inputs, enabling development of innovative, patient-centric solutions Advanced capability in concept generation, feasibility assessment, and simulation-driven design, including development of analytical and computational models to evaluate performance, usability, and risk during early design phasesStrong application of Design for Manufacturability (DFM), Design for Assembly (DFA), and usability/ergonomic principles from concept through development to ensure scalable and robust product designsDemonstrated expertise in early-stage risk identification and mitigation, including application of DFMEA, UFMEA, and hazard analysis to guide concept selection and design refinementStrong command of verification and validation methodologies, with the ability to define testable design inputs and ensure traceability from concept through validation in alignment with ISO 14971 risk management principlesAbility to design and interpret advanced statistical analyses (e.g., DOE, tolerance analysis, feasibility data interpretation) to support concept down-selection, design optimization, and performance characterization
Regulatory and Compliance:In-depth knowledge and application of design control processes and global regulatory requirements (e.g., ISO 13485, FDA 21 CFR 820, EU MDR) in medical device developmentLeads design verification and validation activities, ensuring alignment with regulatory expectations, risk management, and usability engineering principlesOwns and drives change control activities, including ECOs, CAPA, and design changes, ensuring compliance and traceability across the DHF
Process Development and Manufacturing Support:Leads process development and validation activities, including defining and supporting IQ, OQ, and PQ strategies in collaboration with manufacturing and quality teamsDrives PFMEA and risk assessment activities, ensuring alignment between design intent and manufacturing capabilityApplies deep understanding of material behavior and manufacturing processes to optimize product performance, consistency, and yieldProject Management and Collaboration:Authors and reviews complex technical documentation, including design history files (DHF), verification protocols/reports, and regulatory submissionsLeads cross-functional collaboration across R D, Quality, Regulatory, Manufacturing, and Clinical teams, influencing decisions and driving alignmentCommunicates complex technical concepts effectively to diverse audiences, including leadership and external stakeholdersDemonstrates advanced analytical thinking and structured problem-solving, leading root cause investigations and implementing robust solutionsExhibits strong leadership, collaboration, and mentoring capabilities within a matrixed organizationHighly proficient in engineering tools, data analysis platforms, and design/simulation softwareDemonstrated expertise in polymer component design and catheter-based systems, including application to vascular access or interventional devices
Self-motivated, high-energy, positive attitude individual with the initiative and drive for timely completion ofgoals. Able to travel domestically and internationally.
#LI-DR1
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 Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: ... or .... Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rusch, 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.
Job ID: 516572088
Originally Posted on: 4/8/2026
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