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Chemistry Lab Analyst

**Date:** May 21, 2025

**Location:** Morrisville, NC, US

**Company:** Teleflex

**Expected Travel** : None

**Requisition ID** :12203

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™, QuikClot™, LMA™, Pilling™, 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

This role is responsible for conducting residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) testing on sterile medical device products using validated Gas Chromatography (GC-FID) methods. The Chemistry Analyst will provide technical support for laboratory operations, perform data analysis, and lead investigations related to chemical testing nonconformances. This role ensures testing is performed per work instructions, good laboratory practices (GLP), and regulatory standards.

Principal Responsibilities

• Primarily perform validated EO and ECH residual testing on sterile medical devices using GC-FID instrumentation.

• Support method development and method optimization activities for GC-based testing.

• Troubleshoot GC instrumentation and analytical issues, and lead laboratory investigations.

• Review and approve test data and reports according to good documentation practices (GDP).

• Maintain and calibrate GC instruments (GC-FID and GC-MS as applicable).

• Manage laboratory supplies and chemical inventory for chemical testing activities.

• Assist in training junior analysts on GC-based chemical testing methods.

• Support regulatory audits and inspections as a chemistry subject matter expert.

• Execute testing to support sterilization validation, revalidation, and product change assessments.

• Participate in nonconformance investigations and assist in writing CAPAs related to chemical testing.

• Ensure compliance with internal procedures, ISO standards, and FDA requirements.

• May participate in validation for new analytical methods for supporting medical device biocompatibility.

• May perform additional tasks as assigned.

Education / Experience Requirements

• Bachelor’s Degree in Chemistry, Biochemistry, or a related scientific discipline.

• Minimum 2 years experience performing analytical chemistry testing in a regulated laboratory (medical device, pharmaceutical, or similar).

• Hands-on experience with GC-FID and/or GC-MS instrumentation.

• Experience with EO/ECH residual testing strongly preferred.

Specialized Skills / Other Requirements

• Strong understanding of Gas Chromatography theory and applications (FID and/or MS detection).

• Ability to troubleshoot instrument and method performance issues.

• Familiarity with Good Laboratory Practices (GLP) and Good Documentation Practices (GDP).

• Experience working within a Quality Management System (QMS).

• Analytical and critical thinking skills for problem-solving and investigation.

• Proficient in technical writing, including test protocols, reports, and investigations.

• Ability to manage workload autonomously and prioritize tasks effectively.

• Strong verbal and written communication skills.

• Ability to work effectively both independently and as part of a multidisciplinary team.

• Proficiency in Microsoft Office applications (Word, Excel, Outlook).Ability to define, organize, and manage individual tasks

• Ability to coordinate and execute activities involving multiple internal and external functions

• Able to create and review technical documentation

• Interpersonal skills; working in a team and as an individual contributor

• Foster a positive culture of growth, collaboration, and achievement across the organization

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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 [email protected]._

_Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, QuikClot™, 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._

_© 2025 Teleflex Incorporated. All rights reserved._