... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
... Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall ... Post Market Surveillance processes for products and ensure effective execution into the Quality ...
Post Market Surveillance Specialist
Waltham, MA · Hybrid
$46.57 - $57.10/hr
Experience submitting Medical Device Reports (MDRs) and/or adverse event reports to regulatory agencies. * Experience with post-market surveillance activities in accordance with IVDR regulations ...
Post Market Surveillance Specialist
Waltham, MA · Hybrid
$46.57 - $57.10/hr
Experience submitting Medical Device Reports (MDRs) and/or adverse event reports to regulatory agencies. * Experience with post-market surveillance activities in accordance with IVDR regulations ...
Assists with the preparing and submitting post market surveillance reporting including but not limited to Medical Device Reports and Adverse Events to the FDA within regulatory timeframes. * Assists ...
Assists with the preparing and submitting post market surveillance reporting including but not limited to Medical Device Reports and Adverse Events to the FDA within regulatory timeframes. * Assists ...
Quality Assurance Post Market Specialist
Redmond, WA · On-site
$83K - $139K/yr
Preferred * 1 year of post-market surveillance, quality, regulatory affairs, clinical, or related experience within a regulated industry. * Experience within the medical device industry. * Prior ...
Quality Assurance Post Market Specialist
Redmond, WA · On-site
$83K - $139K/yr
Preferred * 1 year of post-market surveillance, quality, regulatory affairs, clinical, or related experience within a regulated industry. * Experience within the medical device industry. * Prior ...
Analyst, Product Surveillance
Plymouth, 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 ...
New
Analyst, Product Surveillance
Plymouth, 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 ...
New
Medical Device Complaint Specialist
Moundsview, MN · On-site
$25 - $27/hr
Support medical device surveillance and post-market vigilance activities. * Maintain knowledge of new products, regulations, and reporting requirements. * Support continuous improvement of complaint ...
Quick apply
Medical Device Complaint Specialist
Moundsview, MN · On-site
$25 - $27/hr
Support medical device surveillance and post-market vigilance activities. * Maintain knowledge of new products, regulations, and reporting requirements. * Support continuous improvement of complaint ...
Medical Device Complaint Specialist
Moundsview, MN · On-site
$24 - $27/hr
... Entry-level medical device safety and complaint investigation role responsible for intake ... Vigilance & Post-Market Surveillance * Complaint Investigation * Adverse Event Reporting (ADE)
Quick apply
Medical Device Complaint Specialist
Moundsview, MN · On-site
$24 - $27/hr
... Entry-level medical device safety and complaint investigation role responsible for intake ... Vigilance & Post-Market Surveillance * Complaint Investigation * Adverse Event Reporting (ADE)
Data Engineer Lead- PMS & QA
Trumbull, CT · On-site +1
$160K/yr
The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA ...
Data Engineer Lead- PMS & QA
Trumbull, CT · On-site +1
$160K/yr
The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical Device performance and Post Market Surveillance activities within the PMS team as well as the broader QA ...
Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...
Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...
Post Market Surveillance Engineer II
$76K - $98K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
Post Market Surveillance Engineer II
$76K - $98K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
Post Market Associate
Waltham, MA · Hybrid
$37.87 - $47.48/hr
This role also supports Post-Market Surveillance (PMS) activities and works closely with cross ... Make reportability determinations and submit Medical Device Reports (MDRs) as required. * Conduct ...
Post Market Associate
Waltham, MA · Hybrid
$37.87 - $47.48/hr
This role also supports Post-Market Surveillance (PMS) activities and works closely with cross ... Make reportability determinations and submit Medical Device Reports (MDRs) as required. * Conduct ...
Regulatory Post Market Surveillance Specialist (Onsite: Sunnyvale, CA) W2 Only
Sunnyvale, CA · On-site
$30 - $38/hr
The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an ... Knowledge and understanding with Medical Device Complaint files and quality record documentation ...
Regulatory Post Market Surveillance Specialist (Onsite: Sunnyvale, CA) W2 Only
Sunnyvale, CA · On-site
$30 - $38/hr
The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an ... Knowledge and understanding with Medical Device Complaint files and quality record documentation ...
Clinical Complaint Specialist
$80K - $100K/yr
Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...
Clinical Complaint Specialist
$80K - $100K/yr
Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...
Clinical Complaint Specialist
Irvine, CA · On-site
$80K - $100K/yr
Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...
Clinical Complaint Specialist
Irvine, CA · On-site
$80K - $100K/yr
Experience with complaint handling, adverse event reporting, post-market surveillance, or quality systems. * Knowledge of FDA Medical Device Reporting requirements (21 CFR Part 803), complaint ...
Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...
Supervises Post-Market Surveillance Specialists by interviewing, training, evaluating job ... Knowledge of medical product/device use. COMPETENCIES * Interpersonal skills * Written and verbal ...
Post Market Surveillance Engineer II
Chaska, MN · On-site
$77K - $99K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
Post Market Surveillance Engineer II
Chaska, MN · On-site
$77K - $99K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
Post Market Surveillance Engineer II
Plymouth, MN · On-site
$76K - $98K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
Post Market Surveillance Engineer II
Plymouth, MN · On-site
$76K - $98K/yr
... Post Market Surveillance processes for Integer under the direction, instruction and guidance from ... medical device or other regulated industry experience preferred). Specialized Knowledge: * While ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs ... COMPETENCIES • Global medical device adverse event reporting, such as MDR, MPR, TGA, and ...
... Post Market Surveillance activities and other governmental inspections as directed. 9. Performs ... COMPETENCIES • Global medical device adverse event reporting, such as MDR, MPR, TGA, and ...
Entry Level Post Market Surveillance Medical Device information
See salary details
$30.5K - $33.3K
1% of jobs
$33.3K - $36K
4% of jobs
$36K - $38.8K
4% of jobs
$38.8K - $41.6K
10% of jobs
$43K is the 25th percentile. Wages below this are outliers.
$41.6K - $44.4K
12% of jobs
$44.4K - $47.1K
17% of jobs
The median wage is $47.6K / yr.
$47.1K - $49.9K
14% of jobs
$52.1K is the 75th percentile. Wages above this are outliers.
$49.9K - $52.7K
17% of jobs
$52.7K - $55.5K
9% of jobs
$55.5K - $58.2K
7% of jobs
$58.2K - $61K
5% of jobs
$30.5K
$47.7K
$61K
How much do entry level post market surveillance medical device jobs pay per year?
As of Aug 15, 2026, the average yearly pay for entry level post market surveillance medical device in the United States is $47,730.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $52,500.00 per year, depending on experience, location, and employer.
What is the difference between Entry Level Post Market Surveillance Medical Device vs Entry Level Quality Assurance Medical Device?
| Aspect | Entry Level Post Market Surveillance Medical Device | Entry Level Quality Assurance Medical Device |
|---|---|---|
| Certifications | Typically requires knowledge of FDA regulations, ISO standards, and basic surveillance tools | Requires understanding of quality standards, audit procedures, and compliance regulations |
| Work Environment | Monitoring device performance, analyzing post-market data, collaborating with regulatory teams | Conducting audits, reviewing manufacturing processes, ensuring product quality |
| Industry Usage | Used in medical device companies focusing on post-market activities and regulatory compliance | Used in quality departments to maintain product standards and compliance |
While both roles involve regulatory knowledge and work within the medical device industry, the Post Market Surveillance role focuses on monitoring device performance after market release, whereas Quality Assurance emphasizes preventing issues through process audits and quality checks.
What cities are hiring for Entry Level Post Market Surveillance Medical Device jobs?
Cities with the most Entry Level 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:
What states have the most Entry Level Post Market Surveillance Medical Device jobs?
States with the most job openings for Entry Level Post Market Surveillance Medical Device jobs include:
Job description
Fulltime opportunity for a Post-Market Surveillance Manager.
This person will lead the development, governance, and integration of Customer Complaints, Medical Device Reporting, Adverse Event Reporting, Corrections and Removals (Recall), and Proactive Post Market Surveillance processes for products and ensure effective execution into the Quality Management System (QMS).
This position is responsible for initiating and supporting quality systems activities in all aspects of the business, including the identification and implementation of continuous process improvement activities.
Maintain oversight, tracking, and escalation for Post Market Processes and take action to ensure processes are maintained per company policies and industry standards.
Qualifications
- Bachelor’s Degree (BA) from a four-year College or University in a technical, engineering, and/or scientific discipline; Master or terminal science degree preferred.
- Professional designations are not required but training and certificates in quality or regulatory affairs would be a plus (e.g., CQM, ASQ, CQE, CQA, RAC, CLIA, Six Sigma, Lean Principles).
- 6+ years experience in a regulated Medical Device or Life Sciences industry with applied experience/knowledge in Investigations, Root Cause Analysis, Complaint Handling, Statistical Analysis, Risk Management, Design Control, Process Validation, FMEA/Risk Assessment, and ISO/QSR;
- At least 1-2 years of Supervisory or Management experience.
About LaBine and Associates
Sourced by ZipRecruiter
LaBine and Associates is a full service talent acquisition firm specializing in executive search for a myriad of industries. Through our partnerships with experienced associates, we can also provide staffing support, expert consultants, and interim executives for your company’s needs. We have deep industry knowledge with understanding in multiple industries. Our specialists include experts in banking/finance, HR/Legal, Technology, Health Care, Life Sciences, Engineering, Energy, Supply Chain, Mining, Agribusiness and manufacturing.
Industry
Professional, scientific, and technical services
Company size
11 - 50 Employees
Headquarters location
San Mateo, CA, US
Year founded
2013