Engineer II

11 days ago

Job Description

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.
Apply 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:

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.

Location

Irvine, CA

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