Controls Specialist at Clairo

Florence, South Carolina, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

ManufacturingIndustries

Requirements

Minimum 5 years’ experience in an engineering role within a manufacturing environment
Advanced working knowledge of PLC programming and ladder logic
Preferred
Bachelor’s degree in Engineering (Electrical, Mechanical or Manufacturing)
Experience in Robotics programming, troubleshooting, and diagnostics (Fanuc / Denso)
Proficient in AutoCAD, Solidworks, Excel, PowerPoint, and other related programs

Responsibilities

Responsible for the continuous improvement of plant processes and equipment including design and PLC program changes, mechanical and electrical documentation, Six Sigma variation reduction, uptime improvements, and maintenance expense reduction
Efficiently uses problem solving techniques including Pareto analysis, cause and effect analysis, multi-variable analysis, FMEA's and DOE's to reach solutions
Provides technical support for plant operations including maintenance support, capital project implementation, and Six Sigma project rollout support
Acts as liaison between plant and Division Engineering personnel in communicating engineering needs, process changes, project reporting, etc
Monitors process, including new equipment and tools, to ensure performance to specifications. Implements capital and non-capital projects
Works with plant quality control and manufacturing personnel to ensure process and equipment is capable of producing product that meets quality and engineering standards

Skills

PLC programming

Ladder logic

AutoCAD

SolidWorks

Excel

PowerPoint

Six Sigma

FMEA

DOE

Pareto analysis

Robotics programming

Fanuc

Denso

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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