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Temporary Post Market Surveillance Jobs (NOW HIRING)

Merit

Senior Manager, Post Market Surveillance

Post Market Surveillance (PMS) documentation processes such as Periodic Safety Update Reports (PSUR) and Post Market Surveillance Reports (PMSR) * Health Hazard Evaluation (HHE) Processes * Field ...

Integer

Post Market Surveillance Engineer II

Plymouth, MN · On-site

$76K - $98K/yr

The primary purpose of this job is to execute and support the Complaint Handling, Regulatory Reporting, and Post Market Surveillance processes for Integer under the direction, instruction and ...

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$107.5K

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

As of Sep 2, 2026, the average yearly pay for temporary post market surveillance 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 temporary post market surveillance role?

A Temporary Post Market Surveillance role involves monitoring the safety and performance of medical devices or products after they have been released to the market. Professionals in this position collect and analyze data on product usage, adverse events, and customer feedback to ensure ongoing compliance with regulatory requirements. The role is typically short-term, supporting projects like product recalls, safety investigations, or regulatory submissions. It is crucial for maintaining product safety and quality, and for reporting findings to regulatory authorities when necessary.

What are some typical challenges faced in a temporary post market surveillance role and how can they be managed?

In a Temporary Post Market Surveillance role, professionals often encounter challenges such as rapidly learning product specifications, interpreting complex regulatory requirements, and managing large volumes of customer feedback or incident reports within tight deadlines. Adapting quickly and seeking guidance from experienced team members can help address these challenges. Staying organized and leveraging digital tracking tools are also essential for efficiently monitoring and reporting product performance and compliance issues. Collaborating closely with regulatory, quality assurance, and product development teams ensures accurate data collection and timely response to potential safety concerns.

What are the key skills and qualifications needed to thrive as a temporary post market surveillance specialist, and why are they important?

To thrive as a Temporary Post Market Surveillance Specialist, you need a background in life sciences or engineering, analytical skills, and familiarity with regulatory requirements such as FDA or EU MDR. Experience with complaint handling systems, data analysis tools, and relevant quality management software is typically required. Strong attention to detail, critical thinking, and effective communication are essential soft skills for investigating product issues and collaborating with cross-functional teams. These skills and qualities are vital to ensure regulatory compliance, safeguard patient safety, and drive continuous product improvement.

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

AspectTemporary Post Market SurveillanceMedical Device Quality Assurance Specialist
CredentialsTypically requires knowledge of regulatory requirements, certifications like ISO 13485, and industry-specific trainingRequires certifications such as ISO 13485, FDA regulations, and quality management system training
Work EnvironmentOften project-based, temporary assignments within medical device companies or consulting firmsFull-time or contract roles within manufacturing or quality departments of medical device companies
Employer & Industry UsageUsed by medical device companies to monitor products post-market and ensure complianceUsed by medical device companies to maintain quality standards and regulatory compliance

Temporary Post Market Surveillance focuses on monitoring and reporting product performance after market release, often in a temporary capacity. Medical Device Quality Assurance Specialists ensure ongoing compliance with quality standards, typically in a more permanent role. Both roles require knowledge of regulatory standards and industry practices, but their focus and employment type differ.

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Temporary Post Market Surveillance jobs near you
Infographic showing various Temporary Post Market Surveillance job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% 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 3 days ago

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)

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