Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Whippany, NJ 07981 The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling ...
Medical Device Cybersecurity Analyst (On Site) Location: York, Pennsylvania Client: Healthcare domain Note: Need someone with a strong healthcare background who can work onsite 3days a week. Job ...
Medical Device Cybersecurity Analyst (On Site) Location: York, Pennsylvania Client: Healthcare domain Note: Need someone with a strong healthcare background who can work onsite 3days a week. Job ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Job Title: Sr. Engineer, Combination Products & Medical Device Location: Columbus, OH Job Type ... Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for ...
Medical Device Engineer or Materials Scientist (Implantable Device Degradation)
Washington, DC · On-site
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
New
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Medical Device Engineer or Materials Scientist (Implantable Device Degradation)
Washington, DC · On-site
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
New
Medical Device Engineer or Materials Scientist (Implantable Device Degradation)
Bethesda, MD · On-site
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
Medical Device Engineer or Materials Scientist (Implantable Device Degradation)
Bethesda, MD · On-site
Medical Device Engineer or Materials Scientist (Implantable Device Degradation) SME Position ... These include, but are not limited to analysis of aspects such as device design and modeling ...
Develop and update Preliminary Hazard Analysis (PHA) in line with risk management procedures ... Experience in medical device development environments, particularly with Design History File (DHF ...
Develop and update Preliminary Hazard Analysis (PHA) in line with risk management procedures ... Experience in medical device development environments, particularly with Design History File (DHF ...
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$18.50 - $24.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$18.50 - $24.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$18.50 - $24.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$18.50 - $24.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Carmel, IN · On-site
$17.75 - $23.75/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Medical Device Coder
Indianapolis, IN · On-site
$18 - $24/hr
Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.
Seasonal Medical Device Analyst information
See salary details
$39K - $44.3K
2% of jobs
$44.3K - $49.6K
1% of jobs
$49.6K - $55K
6% of jobs
$55K - $60.3K
11% of jobs
$60.3K - $65.6K
4% of jobs
$65.7K is the 25th percentile. Wages below this are outliers.
$65.6K - $70.9K
71% of jobs
$70.9K - $76.2K
2% of jobs
$76.2K - $81.5K
2% of jobs
$81.5K - $86.9K
0% of jobs
$86.9K - $92.2K
0% of jobs
$92.2K - $97.5K
1% of jobs
$39K
$68.7K
$97.5K
How much do seasonal medical device analyst jobs pay per year?
As of Aug 15, 2026, the average yearly pay for seasonal medical device analyst in the United States is $68,656.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $69,000.00 per year, depending on experience, location, and employer.
What is the difference between Seasonal Medical Device Analyst vs Medical Device Quality Assurance Specialist?
| Aspect | Seasonal Medical Device Analyst | Medical Device Quality Assurance Specialist |
|---|---|---|
| Credentials | Typically requires a degree in healthcare, engineering, or related field; certifications like CQE are a plus | Requires a degree in life sciences or engineering; often holds certifications like CQE or ISO auditor |
| Work Environment | Primarily in manufacturing plants, labs, or quality control departments, often seasonal or temporary | In quality assurance departments, conducting audits, inspections, and compliance checks |
| Employer & Industry Usage | Used by medical device manufacturers during peak production seasons | Employed across medical device companies to ensure product quality and regulatory compliance |
While both roles involve quality and compliance in the medical device industry, the Seasonal Medical Device Analyst focuses on temporary, seasonal analysis tasks, often during peak production times. The Medical Device Quality Assurance Specialist has a broader, ongoing role in maintaining quality standards and regulatory compliance throughout the product lifecycle.
More about Seasonal Medical Device Analyst jobs
What cities are hiring for Seasonal Medical Device Analyst jobs?
Cities with the most Seasonal Medical Device Analyst job openings:
What are the most commonly searched types of Medical Device Analyst jobs?
The most popular types of Medical Device Analyst jobs are:
What states have the most Seasonal Medical Device Analyst jobs?
States with the most job openings for Seasonal Medical Device Analyst jobs include:
What job categories do people searching Seasonal Medical Device Analyst jobs look for?
The top searched job categories for Seasonal Medical Device Analyst jobs are:
- Business Analyst Training Placement
- Business Analyst Robotic Process Automation
- Remote Food Cost Analyst
- Systems Analyst Hospital
- Remote Life Science Business Analyst
- Hl7 Analyst
- Entry Level Uipath Business Analyst
- Remote Clinical Trials Data Analyst
- Operations Quality Analyst
- Quality Improvement Data Analyst
Contractor
Re-posted 19 days ago
Job description
Company Description
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website http://www.ustechsolutions.com/.We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you
Job Description
Title: Senior Manager Medical Device Safety, Pharmacovigilance
Duration: 12 Months
Location: Whippany, NJ 07981
Job Description:
The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling, regulatory reporting and clinical development for Company medical devices and combination products. The Senior Manager MDS is an expert who provides safety oversight and content contributions to design control, clinical evaluations, vigilance reporting to authorities, trending and post-marketing surveillance for Company Pharmaceutical and Consumer Health medical devices and combination products worldwide.
Position summary:
The incumbent provides counsel as PV medical device subject matter expert to ensure that an effective vigilance, post-marketing surveillance (PMS) and trending systems are implemented and maintained which conforms with global requirements/laws. The Senior Manager MDS works cross-functionally to generate solutions and implement process standards consistent with device industry best practices. The incumbent is a strong problem solver and communicator with a solid understanding of global regulations and standards.
The incumbent will be responsible for the production and accuracy of medical device analysis, interpretation of results and content contributions to PMS and Vigilance activities.
Position duties & responsibilities:
• Provide content input to Project teams for designing, planning and conducting analyses of safety data for the assessment of medical device safety and performance.
• Provide content input to the post-marketing surveillance (PMS) program activities including, PMS system documentation, PMS planning and report management.
• Provide content input, develop and execute PMS trending methodologies, analysis, written contributions and trend report preparations.
• Responsible for monitoring, analyzing and applying trending methodologies to the vigilance data submitted to Health Authorities (e.g MDRs).
• Responsible for the production and accuracy of medical device analysis and interpretation of results.
• Independently review large data sets and prepare reports for submission the Health Authorities under strict timelines and resolved respective queries regarding product safety.
Qualifications
Requirements/Preferences
Education Requirement(s):
• Bachelor's Degree in Engineering, Mathematics or Life-science Discipline with 4 years of professional experience in medical devices or similar sector
Skill & Competency Requirements:
• Strong scientific application of statistical methods used for evaluating complaint trends and establishing thresholds for routine trend reviews (e.g. human factor, malfunction, user interface and user safety)
• Background in medical device trending/signal detection and heavy statistical analysis experience.
• Able to develop and administer management information systems for track and trending.
• Strong analytical and technical skills that include data collection, analysis and required report generation
• Strong communication skills and ability to work both, independently and cross-functionally with Quality, Regulatory, Marketing and other applicable functions within the business
• Working understanding of medical device regulations and industry standards globally specifically 21 CFR 820, 803, ISO 13485, and euMDR 2017/745
Preferences:
The individual should be comfortable working in both office/virtual settings and independently.
Additional Information
All your information will be kept confidential according to EEO guidelines.
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website http://www.ustechsolutions.com/.We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you
Job Description
Title: Senior Manager Medical Device Safety, Pharmacovigilance
Duration: 12 Months
Location: Whippany, NJ 07981
Job Description:
The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling, regulatory reporting and clinical development for Company medical devices and combination products. The Senior Manager MDS is an expert who provides safety oversight and content contributions to design control, clinical evaluations, vigilance reporting to authorities, trending and post-marketing surveillance for Company Pharmaceutical and Consumer Health medical devices and combination products worldwide.
Position summary:
The incumbent provides counsel as PV medical device subject matter expert to ensure that an effective vigilance, post-marketing surveillance (PMS) and trending systems are implemented and maintained which conforms with global requirements/laws. The Senior Manager MDS works cross-functionally to generate solutions and implement process standards consistent with device industry best practices. The incumbent is a strong problem solver and communicator with a solid understanding of global regulations and standards.
The incumbent will be responsible for the production and accuracy of medical device analysis, interpretation of results and content contributions to PMS and Vigilance activities.
Position duties & responsibilities:
• Provide content input to Project teams for designing, planning and conducting analyses of safety data for the assessment of medical device safety and performance.
• Provide content input to the post-marketing surveillance (PMS) program activities including, PMS system documentation, PMS planning and report management.
• Provide content input, develop and execute PMS trending methodologies, analysis, written contributions and trend report preparations.
• Responsible for monitoring, analyzing and applying trending methodologies to the vigilance data submitted to Health Authorities (e.g MDRs).
• Responsible for the production and accuracy of medical device analysis and interpretation of results.
• Independently review large data sets and prepare reports for submission the Health Authorities under strict timelines and resolved respective queries regarding product safety.
Qualifications
Requirements/Preferences
Education Requirement(s):
• Bachelor's Degree in Engineering, Mathematics or Life-science Discipline with 4 years of professional experience in medical devices or similar sector
Skill & Competency Requirements:
• Strong scientific application of statistical methods used for evaluating complaint trends and establishing thresholds for routine trend reviews (e.g. human factor, malfunction, user interface and user safety)
• Background in medical device trending/signal detection and heavy statistical analysis experience.
• Able to develop and administer management information systems for track and trending.
• Strong analytical and technical skills that include data collection, analysis and required report generation
• Strong communication skills and ability to work both, independently and cross-functionally with Quality, Regulatory, Marketing and other applicable functions within the business
• Working understanding of medical device regulations and industry standards globally specifically 21 CFR 820, 803, ISO 13485, and euMDR 2017/745
Preferences:
The individual should be comfortable working in both office/virtual settings and independently.
Additional Information
All your information will be kept confidential according to EEO guidelines.
About US Tech Solutions
Sourced by ZipRecruiter
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.
Industry
It services
Company size
1,001 - 5,000 Employees
Headquarters location
Jersey City, NJ, US
Year founded
2000