Sr. Manufacturing Engineer at Clairo

Holland, Michigan, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Manufacturing, BatteryIndustries

Requirements

Bachelor’s degree in mechanical, electrical, or manufacturing engineering
2–3 years of experience in a manufacturing engineering role
Strong analytical and problem-solving skills with data analysis capabilities
Familiarity with manufacturing process improvement methodologies
Preferred
Proficiency in PLC programming and ladder logic
Experience with robotics programming, troubleshooting, and diagnostics
Working knowledge of AutoCAD, SolidWorks, Excel, and Minitab

Responsibilities

Design, install, and integrate automation solutions for plant machinery and equipment
Lead equipment modifications and enhancements to improve performance and compatibility
Develop business case documentation to support automation initiatives
Coordinate maintenance and repair services, ensuring compliance with manufacturer guidelines
Implement process improvements focused on safety, ergonomics, quality, and productivity
Apply structured problem-solving tools such as A3, KT, and DMAIC (Six Sigma)
Collaborate with plant operations to monitor project progress and identify future opportunities
Analyze trends and present reports to support data-driven decision-making

Skills

PLC programming

Ladder Logic

Robotics programming

AutoCAD

SolidWorks

Excel

Minitab

Six Sigma

DMAIC

Data Analysis

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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