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Company profile

Merit Medical

Merit Medical Systems, Inc.

Healthcare
Product company
Founded
1987
Employees
6,300
Headquarters
🇳🇱 Maastricht (The Netherlands)
Open roles
15 open roles

About

Founded in 1987, Merit Medical Systems, Inc. is a leading manufacturer and marketer of proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care and endoscopy. Merit serves client hospitals worldwide with an international sales force and clinical support team totalling in excess of 500 individuals. Merit employs approximately 6,300 people worldwide. Merit Medical EMEA currently has over 300 employees, spread over more than 20 countries in the EMEA region. Merit Maastricht (The Netherlands) is the European Headquarters and Distribution Center of Excellence.

What people say

3.2Scoreout of 5

Merit Medical has a mixed reputation among employees, with a moderate rating of 3.3 out of 5 on Indeed. While some employees appreciate the work environment, others express concerns about management and growth opportunities.

  • Liked

    Employees appreciate the supportive work environment.

  • Liked

    Many find the company culture to be positive and collaborative.

  • Watch-outs

    Some employees report issues with management and communication.

  • Watch-outs

    Concerns about limited opportunities for career advancement are noted.

  • Theme

    Work-life balance is a recurring topic, with mixed reviews.

Company details

OwnershipPrivate
Business models
B2B
Medical Devices
Locations
Offices
Maastricht, The Netherlands
Maastricht (The Netherlands)
EMEA offices in more than 20 countries

26 observationsLast observed

Open roles

15 open roles

OEM Business Development Manager

Merit Medical, Medical Devices
EligibilityRemote, United States only
Languages
Salary not disclosed

Post Market Surveillance Specialist (Fixed-Term)

Merit Medical, Healthcare
EligibilityRemote, United States only
Languages
post-market surveillanceadverse event reportingFDA regulations (21 CFR 803)Medical Devices Directive (93/42/EEC, as amended)European Medical Device Regulation 2017/745 (MDR)ISO 13485 Quality System StandardsCanadian Medical Device Regulationsmedical device global adverse event reporting
Salary not disclosed

Territory Manager

Merit Medical, Healthcare
EligibilityRemote, Türkiye only
Languages
medical device salessales presentationspricing/contracts preparationcustomer relationship managementMicrosoft Excelword processingdatabase software
Salary not disclosed