Engineering Support Specialist

Date: Feb 19, 2021

Location: Mansfield, MA, US

Company: Teleflex

Expected Travel: Up to 25%

Requisition ID: 3464


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


OEM – Teleflex Medical OEM is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fibers; and bioabsorbable sutures, yarns and resins. 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 position is responsible for the creation, execution and development of medical device documentation used to create, maintain and make changes to data in ERP (Enterprise Resource Planning) software such as bill of materials, routers, and material masters. Responsible for ensuring the sustainability of the Performance Fibers business by managing and implementing ERP changes in a timely manner within the Teleflex Quality systems. In addition, assisting in continuous improvement of manufacturing documentation and ensuring manufacturing processes are aligned with the Quality system requirements

Principal Responsibilities

•    Creates and modifies manufacturing documentation such as BOM’s (Bill of Materials), routers, drawings and procedures.
•    Prepare DCO documentation for manufacturing/R&D for 3 sites.
•    Creates and reviews newly created documentation to ensure accurate information transfer to the manufacturing floor for 3 sites.
•    Revises drawings, procedures, and forms to capture required changes.
•    Assists in the identification of changes to documentation and the ERP system for continuous improvement, and per regulation (i.e. ISO, FDA, Corporate).
•    Executes changes needed to specifications, dwgs or labels with the guidance of engineering and manufacturing.
•    Supports all areas of the organization including R&D, Sales, manufacturing, Quality and Customer Service in order to meet customer requirements, on time delivery and Teleflex corporate metrics. 
•    Participation in the overall product development program management system including regular meetings and discussions around project priorities, status updates.
•    Assists in the creation of documentation required to meet manufacturing and design control requirements.
•    Assists in the development of solutions that will target manufacturability, cost structure, quality, reliability, and overall effectiveness for 3 sites.
•    Initiates and leads new product line extensions as it relates to the addition of currently developed and approved products.
•    Creates and manages product codes, part numbers, BOM’s, routers, material masters and etc. in the ERP and document control systems.
•    Participates in process walks and documentation review for the purposes of developing or improving process flow maps and ensuring consistency to existing procedures..

Education / Experience Requirements

•    Associates/Bachelors degree with 1+ years of relevant experience working in a role which requires documentation preparation and/or coordination.
•    Or, highschool diploma or GED with 3+ years of relevant experience working in documentation preparation and coordination. 
•    Experience in a manufacturing environment preferred (medical device manufacturing a plus).

Specialized Skills / Other Requirements

•    Strong computer skills including Microsoft Office, Word, Excel, Outlook. 
•    Strong working knowledge of and ERP system required; SAP preferred.
•    Strong written and verbal communication skills.
•    Well developed problem-solving and analytical skills.
•    Strong planning and organizational skills.
•    Ability to prioritize work. Sense of urgency to meet deadlines.
•    Customer-focused and service-oriented.
•    Ability to manage and prioritize workload.
•    Ability to work within a team as well as independently.


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®, Rüsch®, UroLift® and Weck® – trusted brands united by a common sense of purpose. Teleflex, the Teleflex logo, Arrow, Deknatel, Hudson RCI, LMA, Pilling, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.

© 2021 Teleflex Incorporated. All rights reserved.

Nearest Major Market: New Bedford