OE Quality Intern (Summer 2026) at Clairo

Plymouth, Michigan, United States

Clairo Logo
Not SpecifiedCompensation
InternshipExperience Level
InternshipJob Type
NoVisa
Automotive, ManufacturingIndustries

Requirements

  • Currently enrolled as a full-time student at an accredited U.S. college or university
  • Pursuing an undergraduate degree in Computer Engineering, Chemical Engineering, Electrical Engineering, Mechanical Engineering, Quality or related field
  • Authorized to work for any employer in the US without the need for sponsorship, now or in the future
  • Based out of Plymouth, MI office location, with ability to travel to sites with regional leadership
  • Hybrid working arrangement – must have a quiet workspace away from interruptions if working remotely and be able to maintain regular contact with supervisor/team via virtual methods

Responsibilities

  • Support in consolidating the customer specific requirements set by the OEM customer with the IATF requirements
  • Create a system to organize the elements of the customer specific requirements from each of the OEM
  • Refine the organization of the customer specific requirements by elements
  • Create a system to manage updates in the customer specific requirements
  • Collaborate with Plant Quality Engineers
  • Work with the Customer Quality Engineers

Skills

IATF Requirements
OEM Requirements
Quality Engineering
Requirements Management
Data Organization
Collaboration

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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