Systems Engineer at Clairo

Milwaukee, Wisconsin, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

AutomotiveIndustries

Requirements

Strong background in battery technology, automotive systems engineering, and compliance with industry standards (ASPICE, ISO 26262, ISO 15288, INCOSE SE Handbook)
Experience with Li-Ion and/or ultra-capacitor battery systems for low-voltage (12V-48V) automotive applications
Proficiency in requirements management tools for traceability between system requirements, architecture, and validation plans

Responsibilities

Capture, analyze, and refine system-level requirements from OEMs, product management, and internal teams
Allocate performance and other limiting requirements to all functional levels
Define system architectures, including cell selection, thermal, electrical, and mechanical interfaces
Develop detailed block diagrams, interface definitions, and system-level schematics
Allocate functional and non-functional requirements to subsystems and components
Manage trade-offs between safety, performance, cost, and scalability
Integrate design work from engineering disciplines
Implement according to the Clarios Functional Safety Process (consistent with ISO 26262) throughout the development lifecycle
Conduct safety analyses such as HARA, FTA, FMEA, and Common-Mode Analysis
Own the system-level DFMEA and coordinate connections with other sub-systems and component FMEAs
Define safety goals, technical safety concepts, and validation strategies
Define and manage thermal, electrical, and mechanical interfaces between the battery pack, BMS, and vehicle powertrain
Work closely with software, mechanical, and electrical teams to optimize system-level interactions
Support Hardware-in-the-Loop (HiL) and Model-in-the-Loop (MiL) testing to validate system integration
Lead the development of Design Verification Plans (DVPs), ensuring comprehensive validation coverage for system performance, durability, and compliance
Document verification coverage of all requirements with traceability in the requirements management tool
Participate in system-level validation, durability testing, and failure mode analysis
Assist in aging studies, thermal modeling, and electrical load analysis for predictive performance assessments
Ensure system and component designs are optimized for manufacturing, assembly, and scalability (DFM)
Work closely with manufacturing, quality, and supply chain teams to refine designs for production feasibility
Support Advanced Product Quality Planning (APQP), contributing to control plan development and DFMEA execution
Release the battery system design to production, ensuring alignment with assembly plant and supplier requirements
Own system-level DFMEA, ensuring proper alignment with subsystem and component-level DFMEAs
Ensure alignment with ASPICE 3.1, ISO 15288, and INCOSE Systems Engineering best practices
Act as a technical liaison between systems, mechanical, and other cross-functional teams

Skills

Li-Ion Batteries

Ultra-capacitors

ISO 26262

ASPICE

ISO 15288

FMEA

HARA

FTA

DFMEA

Requirements Engineering

System Architecture

Functional Safety

System Integration

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters

1972Year Founded

$29.9MTotal Funding

GROWTH_EQUITY_VCCompany Stage

Biotechnology, HealthcareIndustries

5,001-10,000Employees

Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.

The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.

AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.

The company has nearly 50 years of experience in clinical trial technology solutions.

Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.

The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.

Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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