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Internship Risk Management Safety Jobs (NOW HIRING)

Actively participates in facilities committees related to risk management, safety, and quality improvement Job Requirements: * Registered Nurse with a bachelor's degree or related clinical or allied ...

Actively participates in facilities committees related to risk management, safety, and quality improvement Job Requirements: * Registered Nurse with a bachelor's degree or related clinical or allied ...

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Internship Risk Management Safety information

What is the difference between Internship Risk Management Safety vs Risk Management Coordinator?

AspectInternship Risk Management SafetyRisk Management Coordinator
CredentialsTypically pursuing or recent graduate, relevant safety certificationsProfessional certifications like CRM or ARM often required
Work EnvironmentEntry-level, supervised, often in construction, manufacturing, or industrial sitesOffice and site visits, overseeing risk policies and safety procedures
Employer & IndustryInternships in construction, manufacturing, or industrial sectorsCompanies across various industries managing organizational risks

Internship Risk Management Safety roles focus on learning safety protocols and assisting in risk assessments under supervision, while Risk Management Coordinators handle comprehensive risk strategies, policy implementation, and compliance. The internship provides foundational experience, whereas the coordinator role involves more responsibility and expertise.

What cities are hiring for Internship Risk Management Safety jobs? Cities with the most Internship Risk Management Safety job openings:
What are the most commonly searched types of Risk Management Safety jobs? The most popular types of Risk Management Safety jobs are:
What states have the most Internship Risk Management Safety jobs? States with the most job openings for Internship Risk Management Safety jobs include:
Manager, Product Safety Risk Management

Manager, Product Safety Risk Management

JenaValve

Irvine, CA • On-site

$138K/yr

Full-time

Posted 3 days ago


Job description

Job Title: Manager, Product Safety Risk Management
Role Level: Individual Contributor
Supervisor/Manager Title: Vice President Quality and Compliance
Job Location & Environment: Irvine, CA- Corporate Office
Job Description Summary: Manager, Product Safety Risk Management is responsible for leading and advancing product safety risk management across JenaValve's product portfolio, ensuring a consistent, compliant, and risk-based approach from concept through post-market surveillance. This role supports the product safety risk management framework and governance model, helping to drive clear, timely, and well-supported decisions across programs in alignment with ISO 14971, applicable regulatory requirements, design controls, usability engineering, and process risk management.
The Manager serves as a subject matter expert for complex product safety decisions, partners closely with cross-functional stakeholders, and contributes to audits, inspections, and regulatory interactions related to product safety. This is a manager-level individual contributor role with the opportunity to build team leadership responsibilities over time. Success in this role is reflected in effective detection and response to emerging post-market safety signals, strong quality of risk-based decisions, robust risk assessments during product development, and sustained inspection readiness.
Job Responsibilities:
  • Leads execution of the product safety risk management framework and governance model, ensuring consistent application of ISO 14971-aligned practices across the portfolio and throughout the product lifecycle.
  • Develops, implements, and continuously improves policies, procedures, templates, tools, and quality system controls that enable effective and scalable product safety risk management.
  • Provides product safety risk management leadership for complex programs, supporting cross-functional teams with timely, risk-based decision making, escalation, and resolution.
  • Ensures product safety risk management is integrated with design controls, software development lifecycles, usability engineering, process risk management, verification and validation, and post-market surveillance.
  • Oversees the quality and completeness of risk management files and related documentation, including hazard analyses, FMEAs, fault tree analyses, benefit-risk analyses, residual risk evaluations, and Health Hazard Evaluations.
  • Leads post-market safety activities, including safety signal assessment, Health Hazard Evaluations, CAPAs, and cross-functional response planning, to support effective monitoring of product risk performance.
  • Contributes product safety risk management content for regulatory submissions, design changes, and product lifecycle assessments.
  • Partners in audits, inspections, and regulatory interactions related to product safety, helping ensure sustained inspection readiness and effective response to findings and inquiries.
  • Establishes and monitors meaningful metrics to assess the effectiveness of product safety risk management processes and product performance.
  • Promotes a culture of patient safety, accountability, and continuous improvement.

Required Education and Experience:
  • 8-10 years of progressive experience in medical device or healthcare technology, including significant responsibility for product safety risk management in regulated environments.
  • Demonstrated expertise applying ISO 14971 across pre-market and post-market phases, including experience with risk management processes and governance.
  • Strong understanding of design controls and their integration with usability engineering, and post-market surveillance.
  • Proven ability to influence senior stakeholders, lead cross-functional decision making, and communicate complex risk issues with clarity and judgment.
  • Experience leading initiatives or mentoring others in product safety risk management or closely related quality and regulatory functions is preferred.

Skills and Abilities Required for This Job:
  • Advanced knowledge of applicable standards and regulations, including ISO 13485, 21 CFR Part 820, and EU MDR 2017/745.
  • Strong working knowledge of risk management methods and deliverables, including hazard analysis, FMEA, fault tree analysis, benefit-risk analysis, and residual risk evaluation.
  • Experience with quality systems, product development processes, and enabling technologies or work management platforms that support product lifecycle and risk management activities.

Leadership Competencies
  • Exercises sound judgment and operate effectively with a high degree of independence in a complex environment.
  • Drives accountability, collaboration, and continuous improvement across functions while maintaining a strong focus on patient safety and product quality.
  • Demonstrates leadership through influence, partnership, and effective communication across levels of the organization.

Physical Requirements:
  • Travel domestic and international up to10% time.