Quality Inspector- 3rd Shift

Date: Nov 8, 2023

Location: Jaffrey, NH, US

Company: Teleflex

Expected Travel: None

Requisition ID: 9298


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.


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

The Roving Quality Inspector shall support the Jaffrey NH facility, manufacturing departments in the inspection of product and compliance to the quality system, in order to maintain compliance to FDA 21CFR Part 820, ISO 13485 and Teleflex Global and Local procedures.

This position will also provide support in the identification of discrepancies and opportunities for improvement.

Principal Responsibilities

The primary responsibilities and duties include:
•    Inspection of in-process product
•    Verification of process setup, materials, tooling, and sampling 
•    Assisting in training operators to quality system requirements, sampling procedures, and inspection methods
•    Providing resolution to in-process quality issues or concerns
•    Initiation of nonconformances when necessary
•    Providing feedback to value-stream teams on any findings
•    Identifying opportunities for improvement and facilitating those improvements within the Quality System
•    May support with First Article Inspections
•    May assist in reprocessing activities
•    Work closely with manufacturing to support process operations and testing requirements
•    Perform other QA duties as assigned by QE-VST or Quality Manager

Education / Experience Requirements

•    High School Diploma or GED.
•    1 year of manufacturing experience working in medical device manufacturing environment required.
•    Previous Quality Assurance experience preferred.

Specialized Skills / Other Requirements

•    Problem Solving, works well in group problem-solving situations, uses reason when dealing with emotional topics
•    Strong attention to detail; ability to read and interpret prints, procedures, and specifications and demonstrate the ability to be thorough and accurate
•    Knowledge of measurement tools (i.e. micrometers, calipers, vision systems, instrons)
•    Strong understanding of manufacturing record compliance
•    Interpersonal skills that focus on solving conflict, not blaming, maintaining confidentiality, active listening, and is open to new ideas
•    Oral and written communication, communicates in a timely manner, communication is concise, professional, and effective
•    Ability to make quality decisions independently and understand when to escalate
• Self-disciplined to manage time effectively with little supervision
• Problem-solving skills and experience with Root Cause Analysis tools (6M, Cause-Effect, 5Ws etc)
•    Proficiency in MS Word, and Excel required
•    Competent in PowerPoint.
•    SAP ERP knowledge is highly preferred
•    Ability to adapt to shifting priorities 
•    Statistical Techniques and experience with Minitab desired (DOE, SPC, Gage R&R),

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

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.