ZipRecruiter

Log In

1

Post Market Surveillance Medical Device Jobs (NOW HIRING)

Merit

Senior Manager, Post Market Surveillance

Post Market Surveillance (PMS) documentation processes such as Periodic Safety Update Reports (PSUR ... At least twelve (12) years of work-related experience in the medical device industry, of which ...

Fortive

Manager, Customer Quality

The role ensures compliant, timely, and effective execution of complaint handling, medical device reporting, field action coordination, post-market surveillance, customer defect tracking and ...

Tektronix

Manager, Customer Quality

The role ensures compliant, timely, and effective execution of complaint handling, medical device reporting, field action coordination, post-market surveillance, customer defect tracking and ...

New

Fortive

Manager, Customer Quality

Irvine, CA · On-site

The role ensures compliant, timely, and effective execution of complaint handling, medical device reporting, field action coordination, post-market surveillance, customer defect tracking and ...

next page

Showing results 1-20

All JobsPost Market Surveillance Medical Device Jobs

Post Market Surveillance Medical Device information

See salary details

$82K

$96K

$107.5K

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

As of Aug 30, 2026, the average yearly pay for post market surveillance medical device 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 is a post market surveillance medical device?

A Post Market Surveillance (PMS) Medical Device job involves monitoring the safety and performance of medical devices after they have been released to the market. Professionals in this role collect and analyze data from sources like customer feedback, adverse event reports, and clinical studies to ensure compliance with regulatory requirements. They help identify potential risks, implement corrective actions, and contribute to continuous product improvement. Their work ensures patient safety and regulatory adherence while supporting product enhancements and risk mitigation strategies.

What are typical daily responsibilities for a post market surveillance medical device professional?

In this role, you are responsible for monitoring and analyzing data related to medical device performance after the product has been released to the market. This involves reviewing and investigating customer complaints, reporting adverse events to regulatory authorities, and preparing detailed trend analyses to identify any recurring issues. You may also collaborate closely with cross-functional teams such as regulatory affairs, quality assurance, R&D, and clinical teams to address safety concerns and implement corrective actions. Daily tasks often require using specialized databases and documentation systems to track findings and ensure compliance with industry regulations. Working in this role offers a dynamic environment with opportunities to contribute directly to patient safety and ongoing product improvement.

What are the key skills and qualifications needed to thrive in the post market surveillance medical device position, and why are they important?

To thrive as a Post Market Surveillance Medical Device professional, you need expertise in regulatory guidelines (such as FDA, MDR), data analysis, and a background in biomedical or life sciences. Experience with databases, Quality Management Systems (QMS), adverse event reporting tools, and relevant certifications like RAC or Six Sigma are often required. Strong attention to detail, effective communication, and problem-solving skills are essential soft skills for success in this position. These abilities are critical to ensure patient safety, regulatory compliance, and continuous product improvement in a highly regulated medical device industry.

More about Post Market Surveillance Medical Device jobs

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

Cities with the most 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 Post Market Surveillance Medical Device jobs?

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

What job categories do people searching Post Market Surveillance Medical Device jobs look for?

The top searched job categories for Post Market Surveillance Medical Device jobs are:

Post Market Surveillance Medical Device jobs near you
Infographic showing various Post Market Surveillance Medical Device job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $95,950 per year, or $46.1 per hour.

Post Market Surveillance - Quality Engineer

IPG Photonics

Marlborough, MA • On-site

$74K - $96K/yr

Full-time

Re-posted yesterday

IPG Photonics rating

8.2

Company rating: 8.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

131st of 495 rated machine equipment manufacturers

Job description

IPG Photonics is revolutionizing the laser industry as the pioneering developer and leading producer of fiber lasers and amplifiers. Headquartered in Marlborough, MA, IPG has over 4,800 employees in more than 30 locations around the world. We aspire to work together with our employees and customers to apply light in ways that improve life.
Our mission is to develop innovative laser solutions to make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged and thriving workforce that drives a sustainable future for our company and society.
Working at IPG Photonics you can expect challenging projects, a motivating and friendly environment, and competitive benefits.
Job Summary
The Post Market Surveillance Quality Engineer is responsible for monitoring the performance, safety, and quality of IPG Medical devices throughout the post-market lifecycle to ensure compliance with global regulatory requirements and internal quality standards. This role leads or facilitates complaint investigations, failure analysis, adverse event evaluations, and post-market trending activities while collaborating with cross-functional teams to identify product and process improvements. This role works directly with customers to gather accurate complaint information and supports failure analysis, adverse event investigations, and regulatory reporting. The engineer applies quality engineering principles, risk management, and statistical analysis to drive corrective and preventive actions (CAPA), and enhance product reliability, patient safety, and continuous improvement.
Key Responsibilities
  • Lead technical investigations of customer complaints, product failures, and adverse events to determine root cause.
  • Perform trend analysis using complaint and service data to identify emerging quality issues.
  • Apply statistical methods and quality engineering tools to evaluate product performance and support decision-making.
  • 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.
  • Support risk management activities, including updates to risk assessments (ISO 14971) based on post-market surveillance data.
  • 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.
  • Develop metrics, dashboards, and quality reports for management review.
  • 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 regulatory compliance for IPG Medical products.
  • Promote a culture of patient safety, quality, and continuous improvement across the organization.

  • Bachelor's degree in engineering or related field 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
  • Excellent technical writing, communication, and cross-functional collaboration skills
  • Experience with medical device complaint handling systems (preferred)

What IPG Photonics employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply