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Post Market Surveillance Manager Jobs (NOW HIRING)

VERO BIOTECH INC

The Senior Manager, Post-market Surveillance is responsible for the strategic leadership, governance, and continuous improvement of the Post-market Surveillance system for Vero Biotech's combination ...

Integer

Post Market Surveillance Engineer II

Plymouth, MN · On-site

$76K - $98K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food ...

Integer

Post Market Surveillance Engineer II

Chaska, MN

$77K - $99K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food ...

Abbott

Supervisor, Post Market Surveillance

Burlington, MA · On-site

  • Medical

  • Retirement

Manages assigned projects; work cross functionally to identify changes and necessary resources. • ... Preferred Qualifications * 2+ years supervisor role * 2+ years Post-Marker Surveillance experience

Abbott

Supervisor, Post Market Surveillance

Burlington, MA · On-site

  • Medical

  • Retirement

Manages assigned projects; work cross functionally to identify changes and necessary resources ... Preferred Qualifications * 2+ years supervisor role * 2+ years Post-Marker Surveillance experience

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Post Market Surveillance Manager information

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$33.5K

$75.3K

$132.5K

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

As of Aug 16, 2026, the average yearly pay for post market surveillance manager 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 is a post market surveillance manager?

Post Market Surveillance Managers are professionals responsible for monitoring the safety and performance of medical devices or products after they have been released to the market. They collect and analyze data on product usage, adverse events, and customer feedback to ensure ongoing compliance with regulatory requirements. Their role helps identify potential risks, improve product quality, and implement corrective actions if necessary to protect public health.

How does a post market surveillance manager typically collaborate with cross-functional teams to address product safety issues?

As a Post Market Surveillance Manager, you will work closely with teams such as Regulatory Affairs, Quality Assurance, R&D, and Customer Service to monitor product performance and address safety concerns. When an issue is identified, you may lead investigations, coordinate data collection, and facilitate communication between departments to ensure swift resolution and regulatory compliance. This collaborative environment requires strong interpersonal skills and the ability to interpret technical data, ensuring that corrective actions are effectively implemented and documented.

What is the difference between Post Market Surveillance Manager vs Quality Assurance Specialist?

AspectPost Market Surveillance ManagerQuality Assurance Specialist
Required credentialsRegulatory knowledge, certifications like RAPS or ISO auditorQuality management certifications, ISO 9001
Work environmentRegulatory agencies, medical device companiesManufacturing, product development, compliance teams
Employer & industry usageMedical device, pharmaceutical industriesManufacturing, healthcare, biotech sectors
Common search intentRegulatory compliance, post-market monitoringProduct quality, process improvement

The Post Market Surveillance Manager focuses on monitoring and ensuring the safety and compliance of medical devices after they are on the market, often working closely with regulatory bodies. In contrast, the Quality Assurance Specialist concentrates on maintaining product quality during manufacturing and development. While both roles require knowledge of industry standards and certifications, their primary responsibilities and work environments differ, making this comparison useful for professionals exploring career paths or job opportunities in the medical device industry.

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

To thrive as a Post Market Surveillance Manager, you need expertise in regulatory compliance, data analysis, and risk management, typically supported by a degree in life sciences, engineering, or a related field. Familiarity with quality management systems (such as ISO 13485), complaint handling software, and regulatory reporting tools like FDA MedWatch is crucial. Strong attention to detail, problem-solving, and effective communication skills help navigate cross-functional teams and regulatory interactions. These skills ensure the timely identification and resolution of product issues, safeguarding patient safety and maintaining regulatory compliance.
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Post Market Surveillance Manager jobs near you
Infographic showing various Post Market Surveillance Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $75,349 per year, or $36.2 per hour.

Senior Post Market Surveillance Engineer

Imricor Medical Systems Inc

Burnsville, MN • On-site

$110K - $132K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Description:

Supervisor’s Title: Quality Systems Manager
Exempt or Non-Exempt: Exempt

Location: Must be available to work at our location in Burnsville, MN.

Compensation: The expected annual base salary range for this Minnesota-based position is $110,000-132,000. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s knowledge, skills, and or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, and Retirement Benefits).

Basic Function

This Senior Post-Market Quality Engineer position is responsible for ensuring the safety, effectiveness, and regulatory compliance of marketed medical devices throughout their lifecycle. This role supports post-market data analysis and trending, complaint handling, post-market surveillance plans/reports, corrective and preventive action (CAPA), risk management, and other activities. This position collaborates cross-functionally with Regulatory, Clinical, Operations, and R&D to identify trends, investigate product issues, and implement quality improvements that enhance patient safety and product performance.

Essential Functions:

· Collect, analyze, trend, and present post-market data

· Evaluate post-market data to identify emerging issues and drive continuous improvement efforts

· Initiate and support Corrective and Preventive Actions (CAPA) resulting from complaints, audits, trending, and other post-market information

· Authors post market surveillance plans/reports and periodic safety update reports (PSUR).

· Support evaluation of complaints for reportability under applicable FDA, EU MDR, and other global reporting requirements

· Conduct and support complaint investigations to determine root cause and product impact

· Support Health Hazard Evaluations (HHE) and assessment of product issues that may require field actions

· Participate in internal/external audits and support responses related to post-market activities

· Review and update risk management files based on post-market data in accordance with ISO 14971

Performs other related duties and responsibilities, as assigned.

Requirements:

Qualifications:

· Bachelor’s degree in engineering or related field.

· 5+ years’ experience in Post Market Quality or related field

· Experience working in an EU MDR/FDA/ISO 13485 regulated environment.

· Experience in complaint investigations, reporting, risk management (ISO 14971), CAPA, and statistical analysis/trending.

· Strong communication skills, both verbal and written.


Working Conditions

  • Light work, exerting up to 20 lbs. of force or less.
  • Requires clarity of vision at 20 inches or less (near vision) and ability to identify/distinguish colors.
  • Requires typing, talking and hearing.

The statements above reflect the principal function and most significant duties of the job as necessary for its evaluation in relation to other jobs in the organization and shall not be construed as a detailed description of all the work requirements that may be inherent in the job. Any functions that are non-Essential will be identified as such above. A request for Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

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About Imricor

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

51 - 200 Employees

Headquarters location

Burnsville, MN, US

Year founded

2006

Social media

Twitter

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