Regional Manufacturing Engineer at Clairo

St Joseph, Missouri, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Manufacturing, BatteryIndustries

Requirements

Bachelor's or higher in a related discipline or equivalent years of experience
Minimum 5 years’ experience in Manufacturing / Process Engineering with Project Management
Proficiency with AutoCAD, SolidWorks, Excel, Word, PowerPoint, and other related programs
Ability to work effectively across all US plants and internationally at times, with travel up to 50%
Preferred
Prior experience with lead-acid battery manufacturing equipment and processes, including process controls and automation
Proficient in PLC programming, ladder logic creation, and ability to read, explain, and create basic ladder logic
Understanding of the I/O of robotic systems and how PLC interacts with robotic systems, including safety interlocks

Responsibilities

Manage COS/Assembly projects supporting new and existing plant processes
Support plant operations to design/innovate battery manufacturing equipment to meet mid- and long-term safety, quality, and cost KPI targets
Provide resource management and engineering support for Manufacturing Engineering (ME) across all plants, focusing on processes, equipment, and project execution
Lead lean manufacturing initiatives including process layout optimization, equipment integration, and collaboration with maintenance for plant resource issues
Serve as the equipment SME for both new and existing machinery, guiding design, qualification, and troubleshooting efforts
Develop and standardize critical spare parts lists and Total Productive Maintenance (TPM) practices to ensure long-term sustainability
Collaborate with operations, maintenance, and quality teams to drive continuous improvement and cost reduction strategies
Manage end-to-end manufacturing engineering projects including specification development, supplier coordination, equipment installation, and qualification
Mentor and support plant Manufacturing Engineers in executing layouts, PFMEA, SSOW, machine qualifications, and cost tracking
Lead problem-solving efforts on the shop floor, ensuring issues are resolved using sound engineering principles and documented processes

Skills

AutoCAD

SolidWorks

Excel

Word

PowerPoint

Lean Manufacturing

Process Engineering

Project Management

TPM

PFMEA

Equipment Qualification

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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