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Entry Level Post Market Surveillance Medical Device Jobs

Terumo Cardiovascular Group

NY · On-site

$100 - $125/hr

... Medical Device Reporting, and vigilance reporting; collaborate on reportability decisions and timely report generation. Serve as the Post-Market Surveillance subject-matter expert for assigned ...

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Entry Level Post Market Surveillance Medical Device information

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$30.5K

$47.7K

$61K

How much do entry level post market surveillance medical device jobs pay per year?

As of Sep 7, 2026, the average yearly pay for entry level post market surveillance medical device in the United States is $47,730.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $52,500.00 per year, depending on experience, location, and employer.

What is the difference between Entry Level Post Market Surveillance Medical Device vs Entry Level Quality Assurance Medical Device?

AspectEntry Level Post Market Surveillance Medical DeviceEntry Level Quality Assurance Medical Device
CertificationsTypically requires knowledge of FDA regulations, ISO standards, and basic surveillance toolsRequires understanding of quality standards, audit procedures, and compliance regulations
Work EnvironmentMonitoring device performance, analyzing post-market data, collaborating with regulatory teamsConducting audits, reviewing manufacturing processes, ensuring product quality
Industry UsageUsed in medical device companies focusing on post-market activities and regulatory complianceUsed in quality departments to maintain product standards and compliance

While both roles involve regulatory knowledge and work within the medical device industry, the Post Market Surveillance role focuses on monitoring device performance after market release, whereas Quality Assurance emphasizes preventing issues through process audits and quality checks.

What cities are hiring for Entry Level Post Market Surveillance Medical Device jobs?

Cities with the most Entry Level Post Market Surveillance Medical Device job openings:

What are the most commonly searched types of Post Market Surveillance Medical Device jobs?

The most popular types of Post Market Surveillance Medical Device jobs are:

What states have the most Entry Level Post Market Surveillance Medical Device jobs?

States with the most job openings for Entry Level Post Market Surveillance Medical Device jobs include:

Entry Level Post Market Surveillance Medical Device jobs near you
Infographic showing various Entry Level Post Market Surveillance Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $47,730 per year, or $22.9 per hour.

Post Market Surveillance Specialist (Fixed-Term)

Merit Medical

Remote

Full-time

Medical, Retirement, PTO

Posted 27 days ago

Merit Medical Systems rating

7.0

Company rating: 7.0 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

Job description

Work Shift:
DAY
Work Schedule:
Why Merit?
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
This position is a fixed-term opportunity currently expected to run through March 2027.
ESSENTIAL FUNCTIONS PERFORMED
1. Maintains and implements improvement projects and provides training when needed.
2. Interacts with various levels of management, international regulatory affairs/quality assurance, and global regulatory bodies on the adverse event reporting process.
3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies.
4. Participates in complaint related meetings to determine which complaints require an adverse event report.
5. Reviews complaint investigations and makes recommendations for resolution.
6. Prepares and submits necessary reports to global regulatory bodies within the required timeframe for each agency and report type.
7. Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures.
8. Prepares for, participates in and assists with FDA facility inspections, Notified Body Audits, Post Market Surveillance activities and other governmental inspections as directed.
9. Performs other duties and tasks, as needed.
ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS
• Lifting -- Not to exceed 50 lbs. - local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Visual acuity
• Color perception
• Depth perception
• Reading
• Field of vision/peripheral
SUMMARY OF MINIMUM QUALIFICATIONS
• Education and/or experience equivalent to a Bachelor's Degree and three years of related experience in a Quality/Regulatory related field.
• Knowledge of U.S. FDA regulations (21 CFR 803), the Medical Devices Directive (93/42/EEC, as amended), the European Medical Device Regulation 2017/745 (MDR), ISO 13485 Quality System Standards, and Canadian Medical Device Regulations.
• Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc.
• Self-motivated, self-directing, strong attention to detail and excellent time management skills.
• Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.
• Project management experience.
• Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.
PREFERRED QUALIFICATIONS
• American Society for Quality (ASQ) Certifications - Certified Quality Auditor (CQA)
• Regulatory Affairs Certification - RAC (Global).
• Experience with electronic submissions.
COMPETENCIES
• Global medical device adverse event reporting, such as MDR, MPR, TGA, and Vigilance
• Computer skills/internet research
• Interpersonal/communication skills
• Quality system development/training
COMMENTS
Infectious Control Risk Category II:
The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.
As an eligible Merit employee, you can expect the following:
* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights
* Medical/Dental & Other Insurances (eligible the first of month after 30 days)
* Low Cost Onsite Medical Clinic
* Two (2) Onsite Cafeterias
* Employee Garden | Gardening Classes
* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
* 401K | Health Savings Account
To see more on our culture, go to www.merit.com/careers.
Military Veterans are encouraged to Apply.
Merit is a proud Utah Patriot Partner committed to hiring our Veterans.

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