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Post Market Surveillance Rn Jobs (NOW HIRING)

DEKA

Director of Post Market Products

Manchester, NH · On-site

Develop, implement, and continuously improve the post market surveillance (PMS) strategy across DEKA's medical device portfolio, ensuring alignment with FDA regulations, ISO 13485, EU MDR, Canada ...

Integer

Post Market Surveillance Engineer II

Plymouth, MN

$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 ...

Integer

Post Market Surveillance Engineer II

Chaska, MN

$77K - $99K/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 ...

Abbott

Postmarket Surveillance Manager

Saint Paul, MN · On-site

Job Title Post-Market Surveillance Manager Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll ...

Abbott

Postmarket Surveillance Manager

Saint Paul, MN · On-site

Job Title Post-Market Surveillance Manager Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll ...

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Post Market Surveillance Rn information

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$96K

$107.5K

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

As of Jun 9, 2026, the average yearly pay for post market surveillance rn 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 are Post Market Surveillance RNs?

Post Market Surveillance Registered Nurses (RNs) are healthcare professionals who monitor the safety and effectiveness of medical devices or pharmaceuticals after they have been released to the market. They collect and analyze data on product performance, report adverse events, and ensure regulatory compliance. These RNs work closely with manufacturers, regulatory agencies, and healthcare providers to identify potential issues and improve patient safety. Their work helps ensure that products continue to meet safety standards and function as intended throughout their lifecycle.

What are the key skills and qualifications needed to thrive as a Post Market Surveillance RN, and why are they important?

To thrive as a Post Market Surveillance RN, you need a solid nursing background, strong analytical abilities, and an understanding of regulatory requirements, typically with an RN license and experience in clinical or quality roles. Familiarity with adverse event reporting systems, FDA regulations, and safety databases is essential. Exceptional attention to detail, critical thinking, and effective written and verbal communication skills help you excel in this position. These competencies ensure accurate monitoring of medical product safety, regulatory compliance, and protection of patient well-being.

What are the main challenges Post Market Surveillance RNs face when gathering and analyzing product safety data?

Post Market Surveillance RNs often encounter challenges such as managing large volumes of complex data from diverse sources, ensuring accurate and timely reporting, and staying current with evolving regulatory requirements. They must collaborate with cross-functional teams, including clinical, quality, and regulatory departments, to interpret data and develop actionable insights. Effective communication skills and attention to detail are essential to navigate these challenges and ensure patient safety while supporting product improvements.

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

AspectPost Market Surveillance RnMedical Device Quality Specialist
CredentialsRN license, possibly certifications in medical device regulationsQuality certifications (e.g., CQE, ISO auditor)
Work EnvironmentHealthcare settings, hospitals, clinics, regulatory agenciesManufacturing facilities, quality assurance departments
Industry UsageMedical device post-market monitoring, adverse event reportingDevice quality management, compliance, and process improvement

The Post Market Surveillance Rn focuses on monitoring medical devices after they are on the market, ensuring safety and reporting adverse events. The Medical Device Quality Specialist concentrates on maintaining quality standards during manufacturing and ensuring compliance. Both roles require knowledge of medical device regulations but differ in daily tasks and work environments.

Infographic showing various Post Market Surveillance Rn job openings in the United States as of May 2026, with employment types broken down into 85% Full Time, 12% Part Time, and 3% Contract. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $95,950 per year, or $46.1 per hour.
Director of Post Market Products

Director of Post Market Products

DEKA Research and Development

Manchester, NH

Other

Posted 27 days ago

Job description

DEKA Research and Development, on behalf of Millyard Advanced Technologies, located in Manchester, NH, is a dynamic, growing company, focused on the development of new technologies that span a diverse set of applications. At Millyard we are dedicated to using innovative design solutions and state-of-the-art technology to improve lives. We are filled with people who are driven to be among the very best in their respective fields. Consequently, the atmosphere is rewarding and intense. Millyard employees have the opportunity to work on projects that have a positive, enduring impact on millions of people worldwide.
Millyard has an immediate opening for a Director of Post Market Products to lead and oversee all post market surveillance activities in a dynamic medical device research and development environment. This high-visibility leadership role carries significant direct impact on the safety, compliance, and continuous improvement of DEKA's life-changing medical device portfolio. The Director of Post Market Products will report to senior leadership and will be instrumental in driving a culture of proactive risk management and rigorous post market oversight across the organization.
How you will make a difference as Director of Post Market Products:
  • Develop, implement, and continuously improve the post market surveillance (PMS) strategy across DEKA's medical device portfolio, ensuring alignment with FDA regulations, ISO 13485, EU MDR, Canada's SOR-98-282 (CMDR), and other applicable standards.
  • Oversee and direct complaint handling operations, including intake, investigation, trend analysis, and resolution in compliance with 21 CFR Part 803 and 820, EU MDR, and other applicable regulations, ensuring timely and accurate Medical Device Reporting (MDR) submissions.
  • Coordinate cross-organizational failure analysis programs, working with contract development and manufacturing organizations to identify root causes of field failures and drive corrective and preventive actions (CAPAs) to closure.
  • Direct the development and maintenance of Post Market Surveillance Plans, Post Market Clinical Follow-Up (PMCF) plans, and Periodic Safety Update Reports (PSURs) in accordance with EU regulatory requirements.
  • Own and drive the signal detection process, establishing thresholds and trending methodologies to identify emerging safety signals from complaints, MDRs, service data, and literature.
  • Oversee the investigation, documentation, and reporting of product complaints and regulatory reportable events, including failure mode analysis and post market surveillance trend reporting per applicable procedures.
  • Develop and maintain risk-based policies and processes for complaint handling operations to consistently achieve complaint quality objectives.
  • Interface directly with FDA, Notified Bodies, Competent Authorities, and other regulatory agencies on post market matters, including MDR submissions, Adverse Event Reporting, field safety corrective actions (FSCAs), and recall activities.
  • Provide leadership and mentorship to a multidisciplinary team of complaint engineers, failure analysis engineers, and post market specialists.
  • Collaborate with regulatory affairs to ensure post market reporting obligations are met across all markets in which Millyard products are commercialized.
  • Develop and report post market performance metrics to senior leadership, providing clear and data-driven insights into product quality and patient safety.
  • Support internal and external audits, including FDA inspections and Notified Body audits, as the subject matter expert for post market surveillance activities.
  • Establish and maintain procedures and work instructions governing all post market quality activities, ensuring alignment with the MILLYARD Quality Management System (QMS).
  • Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors.
  • Perform other related duties as assigned under management supervision.

Skills needed to be successful:
  • Bachelor's degree in a technical field (engineering, science, or related discipline) required; advanced degree preferred.
  • Minimum of 10 years of experience in the medical device or life sciences industry, with at least 5 years in a post market surveillance, quality, or regulatory role with demonstrated success in a leadership capacity.
  • Deep knowledge of FDA post market requirements, including Medical Device Reporting (MDR) regulations (21 CFR Part 803), Quality System Regulation (21 CFR Part 820) / QMSR, Canada's Medical Devices Regulations SOR-98-282 (CMDR), and Field Safety Corrective Actions.
  • Hands-on experience with EU MDR (Regulation (EU) 2017/745) post market obligations, including PMS plans, PSURs, and PMCF requirements.
  • Demonstrated expertise in failure analysis methodologies (e.g., fault tree analysis, fishbone/Ishikawa, 8D) and the ability to lead cross-functional investigations through to effective CAPA.
  • Strong working knowledge of risk management principles and practices in accordance with ISO 14971, including post-production risk management and benefit-risk analysis.
  • Experience managing and operating within a Quality Management System compliant with ISO 13485 and/or MDSAP.
  • Proven ability to interface with regulatory agencies, including direct experience supporting FDA inspections, and Notified Body audits related to post market activities.
  • Exceptional written and verbal communication skills, with the ability to translate complex technical and regulatory content for diverse audiences.
  • Strong leadership and team management skills, with a track record of building and developing high-performing quality teams.
  • Excellent problem-solving capabilities and sound judgment in a fast-paced, dynamic R&D environment.
  • RAC (Regulatory Affairs Certification) or CQE (Certified Quality Engineer) credential is a plus.
  • Experience with complaint handling software (e.g., Salesforce, MasterControl, TrackWise) is a plus.

About Millyard Advanced Technologies:
https://millyardadvanced.com/
Located in the heart of the Regen Valley in Manchester, NH, our company aims to positively influence the healthcare landscape.

Established 2019Selected Partners
  • Contract Designer:DEKA Research & Development
  • Contract Manufacturer:Merrimack Manufacturing

About DEKA:

One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.

Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

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