Quality Engineer II, Distribution

Quality Engineer II, Distribution

Date: Nov 26, 2025

Location: Olive Branch, MS, US

Company: Teleflex

Expected Travel: Up to 10%

Requisition :13045

The Quality Engineer will be responsible for supporting Quality and Operations, interacting with customers, and providing support for Engineering, Quality Systems, Projects, and Process engineering. Specializations may include:

• Nonconformance and CAPA coordination and processing
• Customer complaint investigations
• Process & product validations
• Customer Notification of Change evaluations
• Internal & external auditing responsibilities and support
• Quality improvement projects
• Maintaining compliance with Teleflex Global & local Procedures and Policies

• Lead nonconformance (NC) and CAPA processing, including Conductor Material Review Board coordination, inspection methods, NC containment/correction/closure, and CAPAs; drive improvement through analysis of trend data.
• Serve as primary investigator and facilitator for Conductor complaint investigation, confirmation, and corrective actions; act as primary customer contact for complaint communications and drive trend‑based improvement.
• Guide and review protocol development, validation implementation, and report review for process validations.
• Lead and participate in key short‑term projects for product or process improvements.
• Maintain company compliance with Quality System Regulations and ISO 13485 standards; experience with FDA and ISO inspections and registration is a plus.
• Perform customer product specification reviews, compile and write training materials, and conduct training sessions on QMS & Quality assurance activities.
• Manage and lead the implementation of continuous improvement projects.
• Provide project management support as needed.
• Develop and initiate standard methods for inspection, testing, and evaluation, utilizing knowledge in related engineering fields.
• Perform any additional QA tasks as assigned by the QA Manager.

• Bachelor’s degree preferred; equivalent ASQ Certified Quality Engineer certification acceptable.
• 3+ years of Quality Assurance experience in a medical device/FDA‑regulated industry.
• Background in engineering or equivalent specialized experience with emphasis in Quality.
• Knowledge of Quality Systems Requirements (ISO 13485, CFR 820 & LATAM).
• Project Management experience preferred.
• Experience with SAP applications desirable.
• Manufacturing or distribution experience preferred.
• Quality certifications (CQE, CRE, CQM, Six Sigma, etc.) a plus.
• Bilingual (Spanish) preferred.
• Relevant experience in medical device, pharmaceutical, or other FDA‑regulated industry is an advantage.

• Experience with 21 CFR 820, ISO 13485, and ISO 14971 risk management.
• Knowledge of corrective action, manufacturing, and design control concepts.
• Computer literacy: statistical software, Excel, Word, PowerPoint, and report generation tools.
• Positive attitude and effective communication with multiple teams and leadership.
• Strong analytical and problem‑solving skills, including Root Cause Analysis tools (6M, Cause‑Effect, 5
  
  Ws, etc.).
• Excellent listening, verbal, written, and interpersonal communication skills.
• Ability to prioritize, adapt to shifting priorities, and work independently with limited supervision.

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:  or