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Post Market Surveillance Rn Jobs (NOW HIRING)

The Post Market Surveillance Senior Manager is responsible for ensuring post-market surveillance processes are compliant, effective, and efficient in line with evolving global regulations. This role ...

The Post Market Surveillance Senior Manager is responsible for ensuring post-market surveillance processes are compliant, effective, and efficient in line with evolving global regulations. This role ...

The Post Market Surveillance Senior Manager is responsible for ensuring post-market surveillance processes are compliant, effective, and efficient in line with evolving global regulations. This role ...

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Post Market Surveillance Rn information

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$82K

$96K

$107.5K

How much do post market surveillance rn jobs pay per year?

As of Jun 7, 2026, the average yearly pay for post market surveillance rn in the United States is $95,950.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $103,000.00 per year, depending on experience, location, and employer.

What are Post Market Surveillance RNs?

Post Market Surveillance Registered Nurses (RNs) are healthcare professionals who monitor the safety and effectiveness of medical devices or pharmaceuticals after they have been released to the market. They collect and analyze data on product performance, report adverse events, and ensure regulatory compliance. These RNs work closely with manufacturers, regulatory agencies, and healthcare providers to identify potential issues and improve patient safety. Their work helps ensure that products continue to meet safety standards and function as intended throughout their lifecycle.

What are the key skills and qualifications needed to thrive as a Post Market Surveillance RN, and why are they important?

To thrive as a Post Market Surveillance RN, you need a solid nursing background, strong analytical abilities, and an understanding of regulatory requirements, typically with an RN license and experience in clinical or quality roles. Familiarity with adverse event reporting systems, FDA regulations, and safety databases is essential. Exceptional attention to detail, critical thinking, and effective written and verbal communication skills help you excel in this position. These competencies ensure accurate monitoring of medical product safety, regulatory compliance, and protection of patient well-being.

What are the main challenges Post Market Surveillance RNs face when gathering and analyzing product safety data?

Post Market Surveillance RNs often encounter challenges such as managing large volumes of complex data from diverse sources, ensuring accurate and timely reporting, and staying current with evolving regulatory requirements. They must collaborate with cross-functional teams, including clinical, quality, and regulatory departments, to interpret data and develop actionable insights. Effective communication skills and attention to detail are essential to navigate these challenges and ensure patient safety while supporting product improvements.

What is the difference between Post Market Surveillance Rn vs Medical Device Quality Specialist?

AspectPost Market Surveillance RnMedical Device Quality Specialist
CredentialsRN license, possibly certifications in medical device regulationsQuality certifications (e.g., CQE, ISO auditor)
Work EnvironmentHealthcare settings, hospitals, clinics, regulatory agenciesManufacturing facilities, quality assurance departments
Industry UsageMedical device post-market monitoring, adverse event reportingDevice quality management, compliance, and process improvement

The Post Market Surveillance Rn focuses on monitoring medical devices after they are on the market, ensuring safety and reporting adverse events. The Medical Device Quality Specialist concentrates on maintaining quality standards during manufacturing and ensuring compliance. Both roles require knowledge of medical device regulations but differ in daily tasks and work environments.

Infographic showing various Post Market Surveillance Rn job openings in the United States as of May 2026, with employment types broken down into 85% Full Time, 12% Part Time, and 3% Contract. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $95,950 per year, or $46.1 per hour.
Post Market Surveillance Specialist

Post Market Surveillance Specialist

IPG Photonics

Marlborough, MA • On-site

Full-time

Posted 14 days ago


IPG Photonics rating

8.2

Company rating: 8.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

94th of 417 rated machine equipment manufacturers


Job description

Job Summary
The Post Market Surveillance Specialist is responsible for monitoring the performance and safety of IPG Medical devices in post-market settings to ensure compliance with global regulatory requirements and to maintain high standards of quality and patient safety. This role works directly with customers to gather accurate complaint information and supports failure analysis, adverse event investigations, and regulatory reporting. The specialist collaborates cross-functionally to identify trends, drive corrective and preventive actions, and promote continuous improvement throughout the product lifecycle.
Key Responsibilities
  • Monitor and evaluate the performance of medical devices in post-market settings to ensure compliance with applicable regulatory requirements and to maintain high levels of safety and quality.
  • Work directly with customers to obtain complete and accurate complaint information and to support failure analysis activities.
  • Conduct thorough and timely investigations of adverse events and complaints related to medical devices.
  • Collaborate with cross-functional teams to gather and analyze data, identify trends, and support the implementation of corrective and preventive actions (CAPA).
  • Develop, maintain, and continuously improve post-market surveillance procedures and processes to ensure compliance with regulatory standards.
  • Maintain accurate, detailed, and audit-ready records of post-market surveillance activities, analyses, and findings.
  • Communicate with regulatory agencies and respond to inquiries or requests related to post-market surveillance activities.
  • Participate in internal and external audits and inspections to demonstrate compliance with regulatory requirements.
  • Stay current on industry regulations, standards, and best practices related to post-market surveillance and communicate relevant updates to internal teams.
  • Provide guidance and support to internal stakeholders on post-market surveillance requirements, processes, and regulatory expectations.
  • Identify opportunities for improvement and drive continuous improvement initiatives to enhance the safety, quality, and performance of IPG Medical devices.
  • Act as a subject matter expert on post-market surveillance and regulatory compliance for IPG Medical products.

Promote a culture of patient safety, quality, and continuous improvement across the organization.
Qualifications
  • Bachelor's degree or equivalent relevant work experience required.
  • At least 3- 5 years of experience in post-market surveillance within the medical device industry.
  • Strong knowledge of medical device regulations and post-market surveillance requirements.
  • Demonstrated attention to detail and ability to manage complex documentation in a regulated environment.
  • Strong analytical, communication, and cross-functional collaboration skills.

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