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Commission Vigilance Jobs (NOW HIRING)

Intern

Elmsford, NY · On-site

$30K - $48K/yr

Benefits: · Based salary plus competitive commission on product and recurring revenue sales. · ... Our core values of Integrity, Vigilance and Helpfulness are proudly demonstrated daily by our ...

Licensed Armed Guard

Mesquite, TX

$16.75 - $21/hr

Completes and maintains proficiency in all requirements and training for Texas Level III Commission ... Constant and dedicated vigilance. * Strong customer service skills, exemplifying Andy Frain ...

Maintains vigilance over the general milieu within the facility to facilitate quality client care ... Commission and other accreditation standards as applicable. * Participates in TQM activities as ...

Maintains vigilance over the general milieu within the facility to facilitate quality client care ... Commission and other accreditation standards as applicable. * Participates in TQM activities as ...

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Commission Vigilance information

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$58.1K

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How much do commission vigilance jobs pay per year?

As of Jun 21, 2026, the average yearly pay for commission vigilance in the United States is $58,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,000.00 and $57,000.00 per year, depending on experience, location, and employer.
What cities are hiring for Commission Vigilance jobs? Cities with the most Commission Vigilance job openings:
What are the most commonly searched types of Vigilance jobs? The most popular types of Vigilance jobs are:
What states have the most Commission Vigilance jobs? States with the most job openings for Commission Vigilance jobs include:
Complaint Reporting MDR/Vigilance Specialist 2

Complaint Reporting MDR/Vigilance Specialist 2

Teleflex

Morrisville, NC

Other

Posted 21 days ago


Teleflex rating

8.2

Company rating: 8.2 out of 10

Based on 26 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: Up to 10%

Requisition ID: 13960

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, Rusch, 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

Work within Complaint Intake & Reporting team to critically review complaints to determine reportability based on the regulatory requirements, risk documentation and clinical experience. Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional information in line with the complaint intake process. Identify potential issues to continuously improve process.

Principal Responsibilities

   Utilizes clinical experience in conjunction with risk management documentation to review complaints for adverse event reportability in accordance with US Canadian & European regulations within required time frames.
   Follows up with health care providers and customers to provide clarification for complaint files and document correspondence to complaint files as required.
   Prepare and submit regulatory reporting documentation such as MedWatch forms with FDA and Vigilance Reports with Canadian and European regulatory authorities.
   Assist as clinical liaison for the complaint management department to facilitate understanding of clinical application for product complaint devices and provide training to other team members as required.
   Utilize complaint management system to accurately document complaint information.
   Final Reviewer/Approval of reporting decisions and initial reports
   Support audit activities are required. Assists with responses to FDA and Competent Authority for additional information queries.
   Work to meet team KPI's Department Metrics and over QA/RA goals and objectives.
   Support improvement projects in the complaint intake and reporting function.
   Support wider QMS and risk management activity as required.

Education / Experience Requirements

   B.S. Degree in Nursing, Biomedical Engineering, or related science discipline with a 2-5 years medical device experience, healthcare, quality, accreditation, or regulatory experience.
   Experience in Post-Market Surveillance, Complaint Handling, Vigilance Reporting, Quality, Risk Management, Clinical Practice, or healthcare accreditation activities (e.g., Joint Commission) preferred.
   Demonstrated knowledge of Medical Device Quality Systems regulations including FDA's 21 CFR 820, 21 CFR 803, ISO 13485:2016, MDD, EU MDR, MDSAP.

Specialized Skills / Other Requirements

   Ability to critically review information and seek clarification.
   Ability to work well under deadlines and pressure in a changing environment.
   Skilled in use of Microsoft suite of applications i.e., Excel, Outlook, and Word.
   The ability to prioritize tasks and be able to manage several tasks simultaneously.
   Ability to read understand and self-educate on emerging regulatory requirements.
BEHAVIORS / VALUES
   Self-driven and ability to work independently and/or as a team player.
   Approachable and enthusiastic. Flexible and adaptable.
   Good judgment and problem-solving ability & is capable of understanding the impact of decision making on both Teleflex Medical and their customers.
   Experience with risk management - preferred.
   Experience with high volume complaints environment - preferred.
   Strong organizational, time management, and influence skills with cultural awareness and sensitivity
   Excellent verbal and written communication skills with ability to lead meetings.

#LI-DR1

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, Rusch, 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.


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