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Medical Device Risk Management Jobs in Florida (NOW HIRING)

Tekhawks LLC

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Validation Engineer - (Medical Device, Pharma)

Jacksonville, FL · On-site

$35 - $40/hr

Skills: * 3-5+ years of validation experience in a medical device, pharmaceutical, or regulated ... Experience with risk assessments, FMEA, and deviation/CAPA management * Proficient in authoring and ...

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VITAS Healthcare

Risk Management Analyst

Miramar, FL · On-site

Claims handling experience in an insurance workers' compensation claim operation and risk management department, with knowledge of workers' compensation statutes and medical management of claims

Medical Device Manufacturing Co

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Manufacturing Engineer II - Medical Device

Pompano Beach, FL · On-site

$80K - $85K/yr

Engineers at this level must have prior relevant experience in the medical device industry and are ... management. • Provide technical and manufacturing engineering support to sustain current ...

HIRE-IQ

Sales Manager - Medical Device

Orlando, FL · On-site

$75K - $100K/yr

HIRE-IQ is recruiting a full-time Sales Manager for a well-established medical device company. The ... Maintain accurate and current records within the company's CRM system * Participate in national and ...

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Medical Device Risk Management information

See Florida salary details

$38.5K

$83.4K

$127K

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

As of Jul 5, 2026, the average yearly pay for medical device risk management in Florida is $83,365.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,300.00 and $96,400.00 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.
What are popular job titles related to Medical Device Risk Management jobs in Florida? For Medical Device Risk Management jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Medical Device Risk Management jobs in Florida look for? The top searched job categories for Medical Device Risk Management jobs in Florida are:
What cities in Florida are hiring for Medical Device Risk Management jobs? Cities in Florida with the most Medical Device Risk Management job openings:
Medical Device Risk Management jobs near you

Validation Engineer - (Medical Device, Pharma)

Tekhawks LLC

Jacksonville, FL • On-site

$35 - $40/hr

Contractor

Posted 3 days ago

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Job description

Position: Validation Engineer

Location: Jackson, FL 

Duration: 1.5-year contract

Hours per week: 40+

Job Description:

We are seeking two mid-level Validation Engineers to support a large capital expansion at a leading medical device manufacturing facility. In this role, you will be responsible for the validation of new manufacturing lines and a high volume of equipment from introduction through final packaging. This is a hands-on, execution-focused role ideal for someone who thrives in a fast-paced, regulated manufacturing environment with a strong attention to detail and documentation rigor.

Skills:

  • 3–5+ years of validation experience in a medical device, pharmaceutical, or regulated manufacturing environment
  • Experience with full validation lifecycle including IQ, OQ, and PQ protocol authoring, execution, and reporting
  • Hands-on experience validating manufacturing equipment such as assembly machines, filling equipment, inspection systems, labeling equipment, and packaging lines
  • Experience with cold storage validation including temperature-controlled units such as freezers and refrigerators (temperature mapping, calibration, qualification)
  • Familiarity with manufacturing line introduction and capital equipment qualification from installation through process validation
  • Strong understanding of FDA regulations, 21 CFR Part 820, and GDP/GMP documentation requirements
  • Experience with risk assessments, FMEA, and deviation/CAPA management
  • Proficient in authoring and managing validation documentation in compliance with quality systems
  • Strong communication skills with ability to work cross-functionally with Engineering, Quality, Operations, and Regulatory teams
  • Experience with eQMS or document management systems a plus