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Post Market Surveillance Medical Device Jobs (NOW HIRING)

Hologic, Inc.

NY · On-site

$170.70 - $303.60/hr

This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain ...

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 ...

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 ...

Abbott

MN · On-site

$30 - $32/hr

The Product Surveillance Analyst supports post-market surveillance activities through the ... Experience in the medical device, pharmaceutical, biotechnology, or regulated manufacturing ...

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

As of Aug 23, 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.

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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.

Director Post Market Compliance

Hologic, Inc.

NY • On-site

$170.70 - $303.60/hr

Other

Posted 18 days ago

Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

180th of 494 rated machine equipment manufacturers

Job description

Hologic is a global leader in medical devices and diagnostics dedicated to improving lives through innovative healthcare solutions. The Director of Post Market Compliance, Corporate plays a critical role in ensuring that the company’s systems for managing product and customer concerns are effective, compliant, and continuously improving. This role leads corporate oversight of complaint handling, post market surveillance, medical device reporting, vigilance, and field actions while collaborating with global teams to maintain regulatory compliance and enhance product quality.

Knowledge
  • Deep understanding of medical device regulatory requirements and compliance standards across domestic and international markets.
  • Knowledge of complaint handling, post market surveillance, medical device reporting, vigilance, and field action processes.
  • Familiarity with FDA-regulated cGMP environments and audit requirements.
  • Understanding of quality management systems and electronic complaint/quality record systems.
  • Awareness of emerging regulatory changes and their impact on post market processes.
Skills
  • Strong leadership and stakeholder management skills with the ability to influence cross-functional and international teams.
  • Strategic and analytical thinking to translate corporate goals into actionable plans.
  • Project and program management capabilities to drive process improvements.
  • Data analysis skills using quality data management tools to identify trends and improvement opportunities.
  • Effective communication and reporting skills for presenting performance metrics and quality insights to senior leadership.
Behavior
  • Demonstrating strong accountability for regulatory compliance and product quality.
  • Collaborative and proactive in working with multiple departments including service, IS, and international teams.
  • Results-driven mindset focused on continuous improvement and operational efficiency.
  • Strong problem-solving approach when identifying compliance gaps and implementing corrective actions.
  • Commitment to fostering a culture of quality and transparency across the organization.
Experience
  • Bachelor’s Degree in business, engineering, science, or a related discipline, or equivalent experience.
  • Minimum of 10 years of progressive experience in quality assurance within the medical device industry.
  • Proven experience managing post market processes such as complaints, vigilance, and field actions.
  • Demonstrated success in managing audits in FDA-regulated cGMP facilities.
  • Experience leading teams, managing projects, and building a strong culture of quality.
Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

The annualized base salary range for this role is $170,700 - $303,600 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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