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Manager Post Market Surveillance Medical Device Jobs

Hologic, Inc.

NY · On-site

$170.70 - $303.60/hr

... surveillance, medical device reporting, vigilance, and field action processes. * Familiarity with FDA-regulated cGMP environments and audit requirements. * Understanding of quality management systems ...

Hologic Inc.

Director Post Market Compliance

Marlborough, MA · On-site

$170K - $303K/yr

... surveillance, medical device reporting, vigilance, and field action processes. * Familiarity with FDA-regulated cGMP environments and audit requirements. * Understanding of quality management systems ...

Fortive

Manager, Customer Quality

... medical device reporting, field action coordination, post-market surveillance, customer defect ... Manage complaint handling execution, including intake, evaluation, investigation, documentation ...

Fortive

Manager, Customer Quality

Irvine, CA

... medical device reporting, field action coordination, post-market surveillance, customer defect ... Manage complaint handling execution, including intake, evaluation, investigation, documentation ...

Abbott

MN · On-site

$30 - $32/hr

Experience in the medical device, pharmaceutical, biotechnology, or regulated manufacturing ... and post-market surveillance processes. Experience working with electronic quality management ...

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Manager Post Market Surveillance Medical Device information

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$33.5K

$75.3K

$132.5K

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

As of Aug 27, 2026, the average yearly pay for manager post market surveillance medical device in the United States is $75,349.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,500.00 and $86,000.00 per year, depending on experience, location, and employer.

What does a manager post market surveillance medical device do?

A Manager of Post Market Surveillance in Medical Devices oversees the monitoring and evaluation of medical devices after they have been released to the market. Their responsibilities include collecting and analyzing data on device performance, investigating complaints or adverse events, and ensuring regulatory compliance with post-market requirements. They also develop strategies to mitigate risks, coordinate with regulatory agencies, and implement corrective or preventive actions to enhance product safety and effectiveness.

What are the key skills and qualifications needed to thrive as a manager post market surveillance medical device?

To thrive as a Manager of Post Market Surveillance in Medical Devices, you need expertise in regulatory compliance, data analysis, and risk management, often supported by a degree in a scientific field and experience with FDA and EU MDR requirements. Familiarity with complaint handling systems, quality management software, and relevant certifications like RAC or Six Sigma are typically required. Strong leadership, problem-solving abilities, and effective communication skills set standout professionals apart. These skills ensure continuous product safety, regulatory adherence, and effective cross-functional collaboration to protect patients and the company's reputation.

What are the main challenges faced by a manager post market surveillance medical device?

One of the main challenges in this role is staying updated with evolving global regulations and ensuring that the company’s post-market surveillance processes comply with all relevant standards. Managers must analyze and interpret large volumes of data from field reports, customer feedback, and adverse event notifications, which requires strong analytical and decision-making skills. Additionally, effective cross-functional collaboration is essential, as you will regularly interact with regulatory affairs, quality assurance, engineering, and customer service teams. Successfully managing these aspects helps ensure product safety, regulatory compliance, and continuous product improvement.

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

AspectManager Post Market Surveillance Medical DevicePost Market Surveillance Specialist Medical Device
CredentialsTypically requires a bachelor's degree, with some roles preferring advanced certifications like RAC or ISO auditorUsually holds a bachelor's degree in life sciences or engineering, with relevant certifications preferred
Work EnvironmentManages teams, oversees surveillance programs, and interacts with cross-functional departmentsConducts surveillance activities, data analysis, and reports under supervision or team guidance
Employer & Industry UsageCommonly employed by medical device companies, regulatory agencies, and consulting firmsFound within medical device companies, regulatory bodies, and quality assurance teams

The main difference is that the Manager Post Market Surveillance Medical Device oversees the entire surveillance program and team, while the Post Market Surveillance Specialist Medical Device focuses on executing surveillance activities and data analysis. The manager has broader responsibilities, strategic planning, and leadership duties, whereas the specialist handles day-to-day surveillance tasks.

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

Cities with the most Manager 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:

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

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

Manager Post Market Surveillance Medical Device jobs near you
Infographic showing various Manager Post Market Surveillance Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $75,349 per year, or $36.2 per hour.

Director Post Market Compliance

NY • On-site

Hologic, Inc.
5 - 10K employees

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

181st of 495 rated machine equipment manufacturers

Good employer

Recommended by parents

Respectful managers

Learn more about Hologic, Inc.external

$170.70 - $303.60/hr

Other

This job post has expired 2 days ago. Applications are no longer accepted.

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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