Quality Specialist II

Date: Nov 6, 2025

Location: Olive Branch, MS, US

Company: Teleflex

Expected Travel: None

Requisition ID: 12963

 

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.

 

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

Growth, Culture, People and Careers: this is the Teleflex Advantage. The Quality Specialist will be expected to provide analytical support to the global ship hold and related process.  The Quality Specialist will monitor and analyze quality restricted material within the distribution center to perform trend analysis and opportunities for improvements.  In addition, this position will support the restriction and release of ship holds and recall material globally

Principal Responsibilities

•    Manage and assist the governance of the Global Ship Hold Process. 
•    Manage and assist in initiating ship holds on behalf of non-Agile PLM sites.
•    Manage and assist with completion of stock assessment/verification (Physical verification of impacted stock) in collaboration with DC operations. 
•    Submit stock assessment quantities in Agile.
•    Manage and assist with any local restriction activities in relation to ship holds. 
•    Manage and assist with ship hold disposition confirmation activities.
•    Manage and assist in verifying and resolving discrepancies of product quantities at all stages of the ship hold process.
•    Incorporate DC Finance, DC Demand Planning, etc. as applicable in the completion of disposition activities.
•    Manage reconciliation and provide any required documentation to support closure of each phase of the product ship hold and the subsequent closure 3PL/DC.
•    Manage and review ship holds to ensure all ship hold DC tasks have been completed and closed.
•    Managing unauthorized ship hold releases in SAP.
•    Completing product batch reports for ship holds in SAP and Agile.
•    Governance of all products contained within the Quality quarantine cage.
•    Complete sample request for external clients.
•    Assist with all Nonconformance sort activities.
•    Assist in restricting and quarantining nonconforming products.
•    Verifying and updating essential product information in SAP.
•    Providing Global Operations with visibility reports in relation open product ship holds
•    Provide KPI metric reports periodically and on request.
•    Own and drive metrics to become a key player in the development of processes to enable and support both the gathering and improving of metrics associated with quality processes. Analyze and identify trends from quality data and develop proactive measures in support of continuous improvement. 
•    All other duties as assigned.

 

Education / Experience Requirements

•    Associates degree in engineering, business, logistics or operations is preferred or 1- 3 year’s equivalent specialized experience with emphasis in Quality or Regulated field preferred. 
•    1-3 years' experience within medical device / FDA regulated industry preferred.
•    1-2 year’s Manufacturing or distribution experience preferred.

Specialized Skills / Other Requirements

•    Strong communication skills, both oral and written with the ability to prioritize and meet deadlines for multiple projects. 
•    Experience with SAP applications is a plus.
•    Ability to work well in a fast-paced environment under pressure and maintain positive, enthusiastic attitude.
•    Eagerness to learn and expand responsibilities.
•    Ability to work effectively in a team environment and build strong working relationships.
•    Experience with systematic project management and problem-solving methodologies is preferred. 
•    Statistical analysis techniques with excellent verbal, written, and presentation skills.

Lead
•    Has a Sense of Purpose & Inspires others
•    Has a desire & ability to “step up”
•    Takes accountability
•    Demonstrates critical judgement 

Engage
•    Communicates with Impact
•    Builds and sustains relationships 
•    Plans and Organizes 
•    Is present & available 

Develop
•    Assist in Developing Leaders
•    Assist in Building High Performance people & teams
•    Invest in personal growth 

Improve 
•    Creates value for the customer 
•    Demonstrates Continuous Improvement via results. 
•    Creates a culture of inclusion & involvement

Demonstrates Functional Mastery
•    Adept at relationship building across functions and geography to effectively work with and leverage centers of excellence. 
•    Excellent computer skills (MS Word, Excel, and PowerPoint) 
•    Detail oriented and strong data driven analytical approach to Quality processes
•    Ability to communicate positively and professionally with employees at all levels of the organization 
•    Resourceful and well organized. High energy level, comfortable performing multifaceted projects in conjunction with day-to-day activities.

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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: 877-880-8588 or Talent@Teleflex.com.

 

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. 
© 2025 Teleflex Incorporated. All rights reserved.