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Medical Device Risk Management Jobs in Greenwich, CT

Cesna Group

Risk Management Analyst

Ridgefield Park, NJ · On-site

$50K - $100K/yr

Job Summary * - Provide support to risk managers for ongoing monitoring and reporting risk ... English and Korean(bi-lingual) What's On Offer * - Full Benefits - Medical, Dental, Vision with ...

American Express

Dir-Risk Management

New York, NY

Comprehensive medical, dental, vision, life insurance, and disability benefits * Flexible working ... Partner with Control Management and other stakeholders to support broader risk, governance, and ...

New

American Express

Dir-Risk Management

New York, NY

Comprehensive medical, dental, vision, life insurance, and disability benefits * Flexible working ... Knowledge of risk management frameworks, regulatory landscape, and methodologies. Preferred ...

New

Jefferies

AVP, Liquidity Risk Management

Manhattan, NY

$150K - $175K/yr

Team The Global Risk Management team is based across the New York, London, Frankfurt, and Asia ... medical condition, physical or mental disability, marital status, domestic partner status, sex ...

Jefferies

AVP, Liquidity Risk Management

Manhattan, NY · On-site

$150K - $175K/yr

Team The Global Risk Management team is based across the New York, London, Frankfurt, and Asia ... medical condition, physical or mental disability, marital status, domestic partner status, sex ...

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Showing results 1-20

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Greenwich, CT

Medical Device Risk Management information

See Greenwich, CT salary details

$57.8K

$125.3K

$190.9K

How much do medical device risk management jobs pay per year?

As of Aug 2, 2026, the average yearly pay for medical device risk management in Greenwich, CT is $125,280.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,100.00 and $144,900.00 per year, depending on experience, location, and employer.

Is risk management a good career?

Risk management in the medical device industry involves identifying and mitigating potential safety and compliance issues, which is essential for product development and regulatory approval. It requires strong analytical skills, knowledge of standards like ISO 14971, and often involves collaboration with engineering and quality teams. The field offers opportunities for growth, specialization, and a stable career path due to the importance of safety in healthcare products.

What is the highest paying risk management job?

In the field of medical device risk management, senior roles such as Risk Management Directors or Chief Risk Officers typically have the highest salaries, often exceeding six figures. These positions require extensive experience, certifications like ISO 14971, and leadership skills, reflecting their strategic importance and responsibility within organizations.

How much does a risk manager get paid?

A medical device risk management professional's salary typically ranges from $70,000 to $130,000 annually, depending on experience, certifications, and location. Senior risk managers or those with specialized skills can earn higher salaries, especially in regulated environments requiring knowledge of ISO 14971 and risk assessment tools.

What are the key skills and qualifications needed to thrive in Medical Device Risk Management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What is risk management in the medical device industry?

Risk management in medical device risk management involves identifying, assessing, and controlling potential hazards associated with medical devices to ensure patient safety and regulatory compliance. Professionals in this field use tools like risk analysis and failure mode effects analysis (FMEA) and often require knowledge of standards such as ISO 14971. Effective risk management is essential throughout the device lifecycle, from design to post-market surveillance.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a Medical Device Risk Management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.
Medical Device Risk Management jobs near you
Infographic showing various Medical Device Risk Management job openings in Greenwich, CT as of July 2026, with employment types broken down into 77% Full Time, 16% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $125,280 per year, or $60.2 per hour.

Medical Device Cybersecurity Analyst

Inficare Technologies

Manhattan, NY • On-site

Full-time

Re-posted 27 days ago

Job description

Position Title: 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 Summary
Looking for someone who watches client's cybersecurity platform for alerts on connected medical devices across hospital clients, triages those findings, and coordinates patches, firmware updates, and mitigations through their work-order system. It's less "penetration tester" and more "asset and risk analyst sitting at the intersection of biomed engineering and infosec.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Monitors and responds to Intelas's comprehensive medical device asset and cybersecurity management platform findings and mitigating steps.
  • Strong knowledge of computers, operating systems, security, and networking
  • Ability to interpret technical documentation and manuals
  • Generate and build bi-weekly, monthly, and quarterly client reports
  • Correlate and perform GAP analysis on discovered medical devices with Intelas's CMMS
  • Create security work orders in Intelas's CMMS and assign to the field as applicable
  • Triage, respond and assign work orders generated from Intelas's CMMS cybersecurity module as appropriate
  • Ensure work orders are completed within defined KPI's and assist on site Intelas resources if needed for successful completion
  • Research and engage OEM's for available approved patches and firmware upgrades
  • Proactively collect most current MDS2 forms
  • Maintain database of approved patches, firmware upgrades and MDS2 forms
  • Collaborate and work with Clients to respond and coordinate mitigating steps and compensating controls on contracted medical devices that may arise from Clients passive asset discovery and risk assessment technology
  • Participate and contribute to Intelas's CEIT Council
  • Maintains operational security metrics to measure the effectiveness of security controls and identify opportunities for improvement
  • Assist in threat intelligence gathering, monitoring of zero-day and correlate to clients CMMS inventory
  • Assist in development and implementation of continued best practices and risk management of inventoried connected medical devices
  • Assures compliance with all regulatory standards including patient safety and all relative criteria governing the safe and appropriate use, testing and management of medical devices.

MINIMUM QUALIFICATIONS:
  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
  • Knowledge of the operation and prior hands-on experience in the maintenance and repair of wide variety of medical equipment and systems
  • High attention to detail and exceptional work quality
  • Experience with process improvement
  • Proven ability to work effectively in an unstructured, fast-paced environment
  • Excellent written and verbal communication skills
  • Overnight travel may be required for Client visits or industry conferences or workshop.

PREFERRED QUALIFICATIONS:
  • Healthcare experience; General knowledge of Biomedical and Diagnostic Imaging
  • Knowledge of healthcare cybersecurity is considered a plus
  • Experience with Computerized Maintenance Management Systems (CMMS)
  • Knowledge of connected medical device asset discovery and risk analysist platforms

EDUCATION:
  • Associates degree in Information Technology or Biomedical Engineering required
  • Security+ within 3 years to 5 years employment (Medical Device)
  • BMET preferred

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