ZipRecruiter

Log In

1

Medical Device Risk Management Jobs in Missouri (NOW HIRING)

Jobgether

Partner closely with technical, quality, product management, supply chain, marketing, and customer ... to medical device and pharmaceutical packaging. * Experience working with major OEMs, Tier 1 ...

Labor Solutions, LLC

Be Seen First

Procurement / Sourcing Manager (MedTech)

Saint Louis, MO · On-site

$120K - $140K/yr

... risk, and support product lifecycle needs while maintaining compliance with medical device ... Experience supporting NPI and product lifecycle management. Skills & Attributes * Strong analytical ...

Coxhealth

Clinical Risk Manager

Springfield, MO

... Management and is responsible for identifying, investigating, analyzing, and mitigating clinical risk across the healthcare system. This role conducts comprehensive investigations of adverse medical ...

CoxHealth

Clinical Risk Manager

Springfield, MO

... Management and is responsible for identifying, investigating, analyzing, and mitigating clinical risk across the healthcare system. This role conducts comprehensive investigations of adverse medical ...

CoxHealth

Clinical Risk Manager

Springfield, MO · On-site

... Management and is responsible for identifying, investigating, analyzing, and mitigating clinical risk across the healthcare system. This role conducts comprehensive investigations of adverse medical ...

CoxHealth

Liability Risk Manager

Springfield, MO

Experience in medical risk management, claims management, or litigation * Skills: * Strong understanding of medical malpractice and general liability claims processes. * Familiarity with healthcare ...

Coxhealth

Liability Risk Manager

Springfield, MO

Experience in medical risk management, claims management, or litigation * Skills: * Strong understanding of medical malpractice and general liability claims processes. * Familiarity with healthcare ...

CoxHealth

Liability Risk Manager

Springfield, MO · On-site

Experience in medical risk management, claims management, or litigation * Skills: * Strong understanding of medical malpractice and general liability claims processes. * Familiarity with healthcare ...

next page

Showing results 1-20

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Missouri

Medical Device Risk Management information

See Missouri salary details

$48.3K

$104.6K

$159.5K

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 Missouri is $104,640.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,400.00 and $121,000.00 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 Missouri? For Medical Device Risk Management jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Medical Device Risk Management jobs in Missouri look for? The top searched job categories for Medical Device Risk Management jobs in Missouri are:
What cities in Missouri are hiring for Medical Device Risk Management jobs? Cities in Missouri with the most Medical Device Risk Management job openings:
Medical Device Risk Management jobs near you
Manager of Engineering - Electrical

Manager of Engineering - Electrical

Bausch + Lomb

Saint Louis, MO • On-site

$119K - $153K/yr

Full-time

Posted 16 days ago

Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

35th of 527 rated manufacturers

Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Objective:
We are seeking a highly experienced and technically proficient Senior Manager to lead our Electronics Design Group within a surgical equipment R&D organization. This role is responsible for overseeing the design, development, and verification of electronic systems for Class II and III medical devices, responsible for the quality and manufacturability of the PCB and cable designs, regulatory compliance and high-quality execution across multiple programs. The ideal candidate has a strong background in electronics design, electronics systems engineering, and team leadership, along with a thorough understanding of IEC 60601 standards, FDA and EU design control regulations, and risk management practices.
Responsibilities:
  • Lead and mentor a multidisciplinary team of electrical engineers, designers and technicians
  • Maintain existing portfolio of 50+ mixed-signal PCBs, including cable interconnections
  • Drive the architecture, design, and implementation of electronics hardware for complex electromechanical and embedded medical device in emerging designs
  • Provide estimates of design project resource and time requirements and design path risks to NPD project managers
  • Oversee all phases of the product development lifecycle (from concept through commercialization) ensuring timely delivery and compliance with regulatory standards.
  • Collaborate cross-functionally with software, mechanical, systems, quality, and internal and external manufacturing teams.
  • Ensure compliance with relevant standards (e.g., IEC 60601, ISO 13485, ISO 14971, IEC 62304).
  • Define and maintain electronics development best practices, tools, design reviews, and documentation.
  • Provide technical leadership in areas including analog/digital design, power management, sensors, wireless communication, and embedded systems.
  • Coordinate with external partners, suppliers, and contract manufacturers when needed.
  • Support regulatory submissions (e.g., FDA 510(k), PMA) and audits as the technical electronics subject matter expert.
  • Participate in long-term strategy and resource planning for the electronics function.
  • Establish and track key performance metrics for engineering deliverables and team development.

Qualifications / Training:
Required:
  • B.S. or M.S. in Electrical Engineering or related discipline.
  • 7-10+ years of experience in electrical systems design in the medical device industry.
  • Technical competence in digital, analog and mixed signal areas.
  • Understanding of both rapid prototyping and production PCB processes
  • Strong understanding of medical device basic safety (IEC 60601-1), medical device design control (ISO 13485), risk management for medical devices (ISO 14971), and regulatory requirements for Class II electronic medical devices.
  • Successful experience with design documentation, DHF/DMR structure, and post-market or acquisition integration work.
  • Familiarity with tools such as Altium and OrCADor equivalent ECAD and Aras PLM document control systems.
  • Experience in assessing mechanical and software design packages.
  • Excellent organizational skills and attention to detail.
  • Strong communication and collaboration skills, especially in cross-functional or cross-company environments, with the ability to clearly and quickly communicate relevant technical issues to non-technical management peers.
  • Self-starting with a demonstrated capacity for both direct contribution and leadership

Preferred:
  • Experience with standards compliance testing and verification.
  • Background in post-merger technical integration or design transfer projects.
  • Experience with legacy systems and reverse engineering documentation gaps

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Our Benefit Programs: Employee Benefits: Bausch + Lomb
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

What Bausch & Lomb employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Bausch & Lomb logo

About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853

View All Bausch & Lomb Jobs

Apply