Job Description

Date: Mar 24, 2026

Location: Jaffrey, NH, US

Company: Teleflex

Expected Travel : Up to 25%

Requisition ID : 13544

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.

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

Leads the Quality function at the Teleflex Medical OEM Jaffrey NH manufacturing facility, ensuring robust, complaint, and efficient delivery on quality and regulatory requirements, through all phases of Customer, product and process lifecycle of Components and Assemblies for the Medical Device Industry.
Manage the development and maintenance of all plant quality systems, ensuring that necessary regulatory and corporate compliance systems are in place and adhered to. This position serves as the Management Representative for the Jaffrey facility. Position is based in Jaffrey NH.

Principal Responsibilities

Driving QMS and Customer Quality requirements throughout product and process lifecycle including NPI, Commercialization, post release feedback and support, Sustaining and End of Life.

Managing and developing the Quality team to assure consistent application of quality standards and regulatory compliance, audit readiness and Customer satisfaction.

Collaborates closely with Plant, Manufacturing and Engineering leadership, to drive operational efficiency while fostering a culture of quality delivery, customer focus, accountability and continuous improvement..

Implementation and maintenance of Quality Management System (QMS) requirements including product realisation and release processes, Supplier quality, external and Internal Audits, Complaint handling, Nonconformances and CAPA investigations, document control, risk management, and change control processes.

Principal Resposnsabilities

• Develop quality systems and establish procedures in compliance to FDA regulations and ISO requirements
• Establish and implement compliance training programs.
• Ensure all manufacturing processes are verified or validated, monitored, and maintained in a state of control, meeting requirements under Customer requirements, FDA 21 CFR 820, ISO 13485, and other applicable regulations.
• Develop and monitor and analyze key performance indicators (KPIs) for quality execution and support Customer Satisfaction driving Continuous Process Improvement.
• Champion a Quality culture of Customer focus, and proactively identifying and implementing process improvements and quality best practices across the VS Work on assigned projects with limited supervision
• Represent Quality for new and existing product improvement, manufacturing transfers, and quality plan initiatives. Support protocol, procedure and specification development
• Complete special assignments as assigned by your Manager
• Generally operate with appreciable latitude for actions or decisions on day-to-day activities; receive guidance on novel or controversial problems
• Outline and implement improvements to Quality System, and processes

Education / Experience Requirements

• B.S. Degree in Engineering, Physical Science, Life Sciences, or a related technical field.
• Minimum of 5 years’ medical device industry experience
• Minimum of 5 years’ related quality experience in a manufacturing environment

• Minimum of 3 years experience supervisory or management experience
• ASQ CQA or CQE certification preferred
• Broad engineering experience in manufacturing operations including new product development, cost reduction, and quality engineering
• Knowledge in textiles, clean room controls, medical device development and device assembly desirable

Specialized Skills / Other Requirements

• Strong leadership and management skills
• Demonstrated experience in mentoring and coaching others
• Regulatory, cGMP, QSR, knowledge base
• Statistical knowledge (DOE, SPC, hypothesis testing, sample comparison)
• Strong computer skills (i.e. database development, statistical software and analysis, word processing for report generation, etc.)
• Strong negotiation and problem-solving skills
• Ability to operate and communicate effectively with multiple teams
• Supplier auditing knowledge and ability (i.e. ASQ-CQA, internal/external courses, seminars)
• Able to understand blueprints, tolerance analysis and related knowledge
• Strong reasoning/analytical skills including the ability to support and prioritize projects and adapt to shifting priorities
• Work with minimal supervision
• Able to successfully resolve problems and conflicts

#LI-NR1

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.
© 2026 Teleflex Incorporated. All rights reserved.

Job Tags

Similar Jobs