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Temporary Post Market Surveillance 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 · On-site

$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 ...

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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 Aug 7, 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 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 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 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.

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.
More about Temporary Post Market Surveillance jobs
What cities are hiring for Temporary Post Market Surveillance jobs? 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? The top searched job categories for Temporary Post Market Surveillance jobs are:
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 49% Full Time, 18% Part Time, 14% Temporary, 14% Contract, and 5% Nights. Highlights an 100% In-person job distribution, with an average salary of $95,950 per year, or $46.1 per hour.

Project Manager - Post Market Products

DEKA Research & Development

Manchester, NH • On-site

Full-time

Re-posted 25 days ago

Job description

DEKA Research and Development, on behalf of Millyard Advanced Medical Products, has an immediate opening for a Project Manager, Post Market Products to support and coordinate post market surveillance and product quality activities in a dynamic medical device research and development environment. This high-visibility role carries significant direct impact on the safety, compliance, and continuous improvement of Millyard’s life-changing medical device portfolio. The Project Manager, Post Market Products will report to the Director of Post Market Products and will play a key role in executing the organization’s post market surveillance strategy and maintaining rigorous oversight of field performance across the product portfolio.
How you will make a difference as Project Manager, Post Market Products:
  • Manage the planning, scheduling, and execution of post market surveillance (PMS) activities across Millyard's medical device portfolio, ensuring alignment with FDA regulations, ISO 13485, EU MDR, Canada’s SOR-98-282 (CMDR), and other applicable standards.
  • Develop and maintain detailed project plans, timelines, and dashboards to track the status of complaint investigations, CAPA closure, MDR submissions, and other post market deliverables, providing regular status updates to the Director of Post Market Products.
  • Coordinate 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.
  • Identify, document, and actively manage project risks and issues, escalating blockers and proposing mitigation strategies to keep post market activities on schedule and in compliance.
  • Facilitate cross-functional meetings and drive accountability across engineering, quality, manufacturing, and regulatory teams to ensure failure analysis investigations and CAPAs progress to closure on time.
  • Coordinate the preparation 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.
  • Contribute to the signal detection process by monitoring complaints, MDRs, service data, and literature against established thresholds and trending methodologies to identify emerging safety signals.
  • 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.
  • Support interactions 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.
  • Collaborate with regulatory affairs to ensure post market reporting obligations are met across all markets in which Millyard products are commercialized.
  • Develop and maintain post market performance dashboards and metric reports, providing clear and data-driven insights into product quality and patient safety for review by senior leadership.
  • Support internal and external audits, including FDA inspections and Notified Body audits, as a subject matter contributor for post market surveillance activities.
  • Author and maintain procedures and work instructions governing 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.
  • Minimum of 5 years of experience in the medical device or life sciences industry, with demonstrated experience in post market surveillance, complaint handling, quality, or regulatory affairs.
  • Demonstrated project management experience, including the ability to develop and maintain project plans, manage competing priorities across multiple workstreams, track deliverables against regulatory deadlines, and communicate status effectively to stakeholders; PMP certification or equivalent is a plus.
  • Proven ability to facilitate cross-functional teams, drive accountability without direct authority, and manage competing stakeholder priorities in a fast-paced environment.
  • Proficiency with project management and collaboration tools such as Microsoft Project, Jira, Smartsheet, or equivalent; experience with complaint handling software (e.g., Salesforce, MasterControl, TrackWise) is a plus.
  • Working 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.
  • Familiarity with EU MDR (Regulation (EU) 2017/745) post market obligations, including PMS plans, PSURs, and PMCF requirements.
  • Working knowledge of risk management principles and practices in accordance with ISO 14971, including post-production risk management and benefit-risk analysis.
  • Experience working within a Quality Management System compliant with ISO 13485 and/or MDSAP.
  • Strong data analysis and reporting skills, with the ability to synthesize post market data into clear metrics, trend reports, and executive summaries.
  • Exceptional written and verbal communication skills, with the ability to convey technical and regulatory content clearly and accurately to diverse audiences.
  • Excellent problem-solving capabilities and sound judgment in a dynamic R&D environment.

About Millyard Advanced Medical Products:
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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