Training Associate
Role Overview
The Training Associate supports the Quality Management System (QMS) training program by administering training assignments, maintaining training records, monitoring training compliance, and supporting training processes related to controlled document changes.
This role works closely with Quality, Manufacturing, Engineering, and other functional teams to ensure training requirements are assigned, completed, and documented in accordance with company procedures and regulatory requirements.
Principal Responsibilities
• Administer and maintain employee training assignments, records, and qualification data within company training systems.
• Monitor training compliance, track completion status, and follow up with employees and managers regarding outstanding training requirements.
• Generate and maintain training reports, metrics, and compliance data to support business and quality objectives.
• Support onboarding and role-transition training assignments and ensure training documentation is accurate, complete, and audit-ready.
• Coordinate training activities associated with controlled document changes and collaborate with document owners and cross-functional teams to identify and implement training requirements.
• Maintain training matrices and support continuous improvement of training administration and compliance processes.
• Ensure training records are maintained in accordance with company policies, quality standards, and regulatory requirements.
• Support internal, customer, and regulatory audits by preparing and providing training records, reports, and related documentation.
• Identify training compliance gaps and communicate issues to appropriate stakeholders for resolution.
• Provide support and guidance regarding training requirements and training records.
• Adhere to all company policies, procedures, and safety requirements.
• Perform other duties and special projects as assigned. Education / Experience Requirements
• High school diploma or equivalent required; Associate degree preferred.
• Minimum of 1 year of experience supporting training administration, document control, quality systems, or a related function within a regulated industry.
• Experience working in a medical device, pharmaceutical, biotechnology, or similarly regulated manufacturing environment. Specialized Skills / Other Requirements
• Working knowledge of Quality Management Systems (QMS) and controlled documentation processes.
• Familiarity with applicable regulatory and quality requirements, including FDA regulations and ISO 13485.
• Experience maintaining records and managing data with a high degree of accuracy. The pay range for this position at commencement of employment is expected to be between $56,500 - $79,100 however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. #LI-EB1 Working Conditions / Physical Demands TRAVEL REQUIRED: 5% WORKING ENVIRONMENT: ☒ Office/Professional ☐ Plant/Manufacturing ☐ Remote/Field ☐ Laboratory 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, ArrowTM, BarrigelTM, DeknatelTM, LMATM, PillingTM, QuikClotTM, RüschTM, UroLiftTM and WeckTM 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.
Full Job Posting
Expected Travel : Up to 10% Requisition ID : 14146 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 ArrowTM, BarrigelTM, DeknatelTM, LMATM, PillingTM, QuikClotTM, RüschTM, UroLiftTM and WeckTM – 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
The Training Associate supports the Quality Management System (QMS) training program by administering training assignments, maintaining training records, monitoring training compliance, and supporting training processes related to controlled document changes.
This role works closely with Quality, Manufacturing, Engineering, and other functional teams to ensure training requirements are assigned, completed, and documented in accordance with company procedures and regulatory requirements.
Principal Responsibilities
- Administer and maintain employee training assignments, records, and qualification data within company training systems.
- Monitor training compliance, track completion status, and follow up with employees and managers regarding outstanding training requirements.
- Generate and maintain training reports, metrics, and compliance data to support business and quality objectives.
- Support onboarding and role-transition training assignments and ensure training documentation is accurate, complete, and audit-ready.
- Coordinate training activities associated with controlled document changes and collaborate with document owners and cross-functional teams to identify and implement training requirements.
- Maintain training matrices and support continuous improvement of training administration and compliance processes.
- Ensure training records are maintained in accordance with company policies, quality standards, and regulatory requirements.
- Support internal, customer, and regulatory audits by preparing and providing training records, reports, and related documentation.
- Identify training compliance gaps and communicate issues to appropriate stakeholders for resolution.
- Provide support and guidance regarding training requirements and training records.
- Adhere to all company policies, procedures, and safety requirements.
- Perform other duties and special projects as assigned. Education / Experience Requirements
- High school diploma or equivalent required; Associate degree preferred.
- Minimum of 1 year of experience supporting training administration, document control, quality systems, or a related function within a regulated industry.
- Experience working in a medical device, pharmaceutical, biotechnology, or similarly regulated manufacturing environment. Specialized Skills / Other Requirements
- Working knowledge of Quality Management Systems (QMS) and controlled documentation processes.
- Familiarity with applicable regulatory and quality requirements, including FDA regulations and ISO 13485.
- Experience maintaining records and managing data with a high degree of accuracy. The pay range for this position at commencement of employment is expected to be between $56,500 - $79,100 however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. #LI-EB1 Working Conditions / Physical Demands TRAVEL REQUIRED: 5% WORKING ENVIRONMENT: ☒ Office/Professional ☐ Plant/Manufacturing ☐ Remote/Field ☐ Laboratory 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, ArrowTM, BarrigelTM, DeknatelTM, LMATM, PillingTM, QuikClotTM, RüschTM, UroLiftTM and WeckTM 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.
About Teleflex Incorporated
Global provider of medical technology solutions for healthcare.
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