Regulatory Affairs Specialist - United States

Expected Travel: Up to 10% · Requisition ID: 13313 · 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 healthc ...

Job description

Expected Travel: Up to 10%

Requisition ID: 13313

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

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.

Position Summary

This is a mid-level Regulatory Affairs position responsible for integrating regulatory knowledge throughout the product lifecycle and coordinating projects effectively. The role supports the Regulatory Affairs team by communicating regulatory strategies and preparing essential documentation for market authorizations. Additionally, the position involves maintaining regulatory information systems. Strong communication and technical writing skills are essential to succeed in this role. 

INDIVIDUAL CONTRIBUTORS:

•    Commitment to Goals –A strong commitment to achieving goals is essential for personal and team success. It requires taking ownership of tasks, staying focused on priorities, and consistently delivering high-quality work. Being proactive, managing time effectively, and seeking support when needed are critical to meeting deadlines and overcoming challenges. By aligning personal efforts with team and organizational objectives, individual contributors play a vital role in driving results and advancing shared goals.

•    Continuous Improvement - Continuous improvement means actively seeking ways to enhance your work, skills, and contributions. It's critical to stay curious, embrace feedback, and look for opportunities to streamline processes or solve problems more effectively. Individual contributors should take initiative to learn from experiences, adapt to change, and apply new knowledge to drive better outcomes. By consistently striving to improve, they add value to their team and support the organization's growth and success.

•    Culture and Values – Living our culture and values is essential to fostering a positive, collaborative work environment. Individual contributors demonstrate this by treating others with respect, acting with integrity, and contributing to an inclusive and supportive team culture. It's critical to hold oneself accountable, align actions with shared values, and support the broader mission of the organization. By consistently modeling these behaviors, individual contributors help strengthen the workplace culture and positively influence those around them.

Principal Responsibilities

•    Participate in multidisciplinary teams and communicate regulatory requirements effectively

•    Provide regulatory input to product lifecycle planning

•    Obtain and evaluate regulatory impact of proposed design and manufacturing changes to commercially distributed medical devices

•    Conduct appropriate research to develop strong regulatory strategies for new products

•    Determine issues that may create regulatory obstacles and investigate solutions

•    Prepare and submit applicable regulatory documentation, as required (with focus on the US, EU and Canadian markets) and/or compile necessary documentation as requested by International Regulatory Affairs personnel

•    Monitor progress of submission reviews and interact with regulatory agencies, as  appropriate

•    Participate in risk management assessments

•    Review and approve product labeling, advertising, and promotional information for regulatory compliance

•    Assist with SOP development and implementation

•    Maintain regulatory information systems

•    Support device import/export and distribution control activities

•    Support regulatory compliance initiatives

•    Monitor the impact of changing and evolving global regulations on submissions, practices, and procedures, and communicate to appropriate personnel

•    Other duties as assigned by the Regulatory Affairs management team

•    Adhere to and ensure the compliance of Teleflex's Code of Ethics, all Company policies, rules, procedures, and housekeeping standards

Education / Experience Requirements

•    Associate or Bachelor's degree, preferably in the science or engineering disciplines

•    Must have 2-5 years in a medical device organization, preferably in regulatory affairs

•    Previous US, Canadian, and EU submissions experience preferred

•    RAC certification preferred

•    Ability to apply business and Regulatory Affairs ethical standards; analytical and critical thinking skills

•    Proficient in Microsoft Office Suite

Specialized Skills / Other Requirements

•    Must be a well-organized self-starter who takes the initiative for independent work with attention to detail and has the ability to follow written and verbal instructions.

•    Manage assigned projects and related activities, propose market authorization strategies, effectively participate on cross-functional teams, and identify and solve mid-level problems.

•    Must possess a basic understanding of product risk/benefit concepts, working knowledge of US and International regulations applicable to market authorization for Vascular products, good verbal communication, technical writing, intra- and interdepartmental communication, and collaboration skills.

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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, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. 
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