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Engineer II

Irvine, CA, US • Posted 1 day ago • Updated 12 hours ago

Full Time

On-site

Fitment

Dice Job Match Score™

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Job Details

Skills

Research and Development
SAFE
Product Design
Regulatory Compliance
Use Cases
System Requirements
Requirements Traceability
Systems Architecture
System Integration
Reporting
Verification And Validation
Collaboration
Systems Design
Pharmaceutics
Documentation
IT Management
Analytical Skill
Problem Solving
Conflict Resolution
Decision-making
ISO 9000
ISO 13485
Design Controls
Medical Devices
Systems Engineering
Traceability Matrix
Risk Management
FMEA
Risk Assessment
Communication
Product Development

Research and Development
SAFE
Product Design
Regulatory Compliance
Use Cases
System Requirements
Requirements Traceability
Systems Architecture
System Integration
Reporting
Verification And Validation
Collaboration
Systems Design
Pharmaceutics
Documentation
IT Management
Analytical Skill
Problem Solving
Conflict Resolution
Decision-making
ISO 9000
ISO 13485
Design Controls
Medical Devices
Systems Engineering
Traceability Matrix
Risk Management
FMEA
Risk Assessment
Communication
Product Development

Summary

Job Description:

We are seeking a Systems Engineer II to join a Device and Combination Product Development - R&D team. The engineer will contribute to the development and launch of innovative drug-device combination products.
The role will integrate multiple engineering disciplines to support robust, safe, compliant, and patient-focused product design and performance.

Responsibilities:

Develop and maintain Design History Files (DHF) and Design Control documentation in compliance with applicable regulations.
Define User and Stakeholder Needs and perform Use Case Analysis.
Develop and maintain Design Inputs, System/Sub-System Requirements, and requirements traceability.
Perform Standards Coverage Analysis.
Support System Architecture and System Integration activities.
Integrate third-party development activities into the overall product development process.
Develop and support Risk Management Plans, risk assessments, and risk reporting.
Conduct or support FMEA and Use Error Risk Assessments.
Support integration of drug product development activities.
Support design verification and validation activities.
Collaborate across engineering and cross-functional teams to meet project objectives.
Provide technical leadership and influence stakeholders within a matrixed organization.
Support implementation and improvement of Systems Engineering principles.
Ensure system design and documentation meet applicable safety, quality, and regulatory requirements.
Identify project risks and develop appropriate mitigation strategies.
Support project schedules, priorities, and competing deliverables.
pply strong analytical and decision-making skills to resolve technical challenges.

Qualifications:

Bachelor's degree: Typically, 5-10 years of relevant experience.
Master's degree: Typically, 3-7 years of relevant experience.
PhD: Typically, 1-4 years of relevant experience.
Strong theoretical and practical understanding of the relevant scientific/engineering discipline.
Experience developing products within a regulated industry, particularly Medical Device, Pharmaceutical, Biotech, or Combination Product environments.
Experience with Design Controls, DHF, requirements definition, traceability, risk management, and product architecture.
Strong written and verbal communication skills.
Experience preparing technical, scientific, or regulatory documentation.
Demonstrated technical leadership and ability to influence and negotiate internally and externally.
Strong analytical, problem-solving, organizational, and decision-making skills.
Self-driven, proactive, and comfortable working in a cross-functional/matrixed environment.
Regulatory & Industry Standards

Experience with relevant standards and regulations, including:

IEC 60601.
ISO 14971.
IEC 62304.
ISO 11608.
ISO 11040.
ISO 13485.
21 CFR 820.
MDR.
FDA/regulatory requirements for medical devices and combination products.

Top Skills Required:

Design Controls experience in Medical Device or Combination Product development.
Systems Engineering experience, including Design Inputs and Traceability Matrix.
Risk Management experience, including Risk Management Plans, FMEA, and risk assessments.
Strong written and verbal communication skills.
Experience working in a regulated product-development environment.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: ac9d600692fdb6318626c800864f98e5
Posted 1 day ago

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