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MDR Regulatory Affairs Specialist at Teleflex

Posted in Compliance 14 days ago.

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Type: Full Time
Location: Morrisville, North Carolina





Job Description:

Location: Morrisville, NC, US

Company: Teleflex

Expected Travel: Up to 25%

Requisition ID: 170

About Teleflex Incorporated

Teleflex is a global provider of clinically effective medical technologies designed to improve the health and quality of people s lives. We apply purpose driven innovation a relentless pursuit of identifying unmet clinical needs to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, interventional cardiology, surgical, anesthesia, cardiac care, interventional urology, urology, emergency medicine and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference. For more information, please visit teleflex.com.

Global Functions The Corporate division is the central operating unit of the company; setting strategy and policy and providing business development, finance, human resources, information technology, investor relations and legal support to the businesses. The global Company headquarters is located just outside of Philadelphia in Wayne, PA. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients lives.

POSITION SUMMARY

Responsible for assessing gap assessments and preparing updates to technical documentation that are required to meet the EU MDR requirements. Participate and interface with teams to address and execute the transition from the Medical Device Directive to the Medical Device Regulation. Products will include all classifications, i.e. Class I, IIa, IIb and III. The position will require basic knowledge to be capable of interfacing and assessing documents from various departments such as Clinical Affairs, R&D, Quality Engineering and BU Regulatory Affairs.

The candidate will participate in any resultant compliance activities, resulting from the review of the technical documentation.

PRINCIPAL RESPONSIBILITIES

* Review and understand gap assessments on Technical Files and Design Dossiers against MDR requirements. This will require a review of all technical documentation, including, but not limited to, design verification & validation protocols & reports, risk management files, usability protocols & reports, manufacturing process information, biocompatibility evaluation reports, list of applicable standards, list of general safety and performance requirements, declaration of conformity and clinical data.

* Support the collection and provision of data required to submit to EUDAMED.

* Work with Project Manager & BU lead to determine implementation plan to complete updates to technical documentation.

* Work with BU regulatory and MDR program work stream leads to ensure technical documentation update timelines are aligned.

* Participate in regulatory impact assessments as it relates to the MDR and relay the information to product specific RA team member and/or design teams.

* May serve as MDR RA team member for promotional materials review and product labeling as they relate to MDR registration and commercialization of medical devices.

* May support new product development teams to assure collection of appropriate data for MDR regulatory submissions and compliance.

* Identify use of appropriate International standards.

* Work in coordination with MDR PM to Monitor MDR government agency laws and regulations through websites and publications.

* Provide guidance to junior members of the Regulatory Affairs staff as related to the MDR project.

* Brings MDR Regulatory Affairs questions/issues to the attention of MDR Project Management team and Business Units leads.

* Report out for specific BU project status to Core Team and potentially MDR Steering Committee.

* Determine issues which may create regulatory obstacles; investigate and propose solutions

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

EDUCATION / EXPERIENCE REQUIREMENTS

* Minimum of a Bachelor's degree

* Minimum of 2-4 years' experience working in a FDA or ISO regulated environment.

* The ideal candidate would have a degree in a scientific discipline such as biology, microbiology, chemistry, engineering, or medical technology.

* Experienced in the skillful preparation of technical files and design dossiers

SPECIALIZED SKILLS / OTHER REQUIREMENTS

* Orientation for detailed work with emphasis on accuracy and completeness

* Effective written and oral communication skills

* Good organizational and planning skills; drives for results

* Effective analytical/problem solving skills

* Good interpersonal skills that include working well in a team environment and the ability to lead others.

* Ability to exercise reasonably independent judgment and discretion within a defined range of policies and practices.

* Ability to handle multiple tasks and to prioritize/schedule work to meet business needs with routine supervision.

* Working knowledge of international requirements and quality systems.

* Computer Literate: Microsoft Office -- PC, Word, Excel, PowerPoint

Teleflex, Inc. is an affirmative action & equal opportunity employer. D/V/M/F. Applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 262-439-1894.

Teleflex is the home of Arrow , Deknatel , Hudson RCI , LMA , Pilling , R sch , UroLift and Weck trusted brands united by a common sense of purpose. Teleflex, the Teleflex logo, Arrow, Deknatel, Hudson RCI, LMA, Pilling, R sch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/