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Temporary Post Market Surveillance Jobs (NOW HIRING)

Apex Systems

Post Market Analyst

Burlingame, CA · On-site

$35 - $40/hr

This role will focus on post-market surveillance (PMS), complaint investigations, and customer quality activities supporting regulated products. The ideal candidate will have experience handling ...

Hologic Inc.

Post Market Quality Specialist 2

Newark, DE · On-site

$92K - $144K/yr

The Specialist owns and leads the Post Market Surveillance Review Boards (PMS RBs), presenting product performance metrics, trend summaries, and identified signals requiring follow up. Working in ...

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 ...

Fortive

Manager, Customer Quality

Irvine, CA

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

BioTalent

Director Clinical Affairs

Santa Rosa, CA · On-site

$164K - $216K/yr

Own the full device/SaMD clinical lifecycle -- from early-stage study design through trial execution, final study report, and post-market surveillance * Develop study design from scratch in close ...

BioTalent

Director Clinical Affairs

Mundelein, IL · On-site

$153K - $202K/yr

Own the full device/SaMD clinical lifecycle -- from early-stage study design through trial execution, final study report, and post-market surveillance * Develop study design from scratch in close ...

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Temporary Post Market Surveillance information

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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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Cities with the most Temporary Post Market Surveillance job openings:

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

The most popular types of Post Market Surveillance jobs are:

What states have the most Temporary Post Market Surveillance jobs?

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

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

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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 Quality Engineer- Essential Wound Care

Medline

Chicago, IL • On-site

$79K - $119K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 12 days ago

Medline Industries rating

7.6

Company rating: 7.6 out of 10

Based on 252 frontline employees who took The Breakroom Quiz

229th of 545 rated manufacturers

Job description

Job Summary
Job Description
The Post-Market Quality Engineer is responsible for monitoring product performance in the field, overseeing complaint trends, and assisting with escalated investigations when necessary. This role ensures compliance with global regulatory requirements and drives continuous improvement through data analysis, risk-based testing, and collaboration with cross-functional teams to maintain product safety and effectiveness.
Key Responsibilities
  • Lead post-market surveillance and trending by analyzing complaint data, defective products, and field performance metrics to identify trends, generate quarterly and annual reports, and implement corrective actions using statistical methods.

  • Conduct root cause analysis for escalated complaints, develop and execute test plans, and coordinate risk-based product testing with internal and external laboratories, including competitor product analysis as needed.

  • Maintain compliance with FDA 21 CFR 820, ISO 13485, EU MDR, and other global regulations for post-market activities, including health hazard evaluations, recalls, adverse event reporting, and change controls, while supporting audit readiness and regulatory inspections.

  • Lead investigations of non-conformances, implement effective corrective and preventive actions (CAPA), and collaborate with suppliers on SCARs, qualification requirements, and quality improvement initiatives.

  • Contribute to the maintenance of the Quality Management System (QMS) through internal audits and management reviews, and track and report post-market KPIs to ensure proactive risk management and continuous improvement.

Education & Experience
  • Bachelor's degree in Engineering, Science, or related technical field.

  • 2+ years of experience in Quality or Engineering; medical device industry experience preferred.

Skills & Qualifications
  • Strong knowledge of post-market surveillance, complaint handling, and risk management (ISO 14971).

  • Working knowledge of government and industry quality assurance codes and standards (e.g. 21 CFR 820, ISO13485).

  • Proficiency in statistical analysis tools and MS Office Suite.

  • Experience with QMS software and complaint handling systems

  • Excellent problem-solving, communication, and cross-functional collaboration skills.

  • Ability to manage multiple projects and meet deadlines with minimal supervision.

  • Up to 15% travel required.

Preferred Qualifications
  • 2+ years of industry experience in Medical Devices, Drugs, and/or fields directly related to the role.

  • Hands-on experience with post-market surveillance activities, including complaint trending, root cause investigations, and risk-based decision making for corrective actions.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$79,000.00 - $119,000.00 Annual
The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966

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