Supplier Quality Lineas Adyacentes at Clairo

San Pedro Garza García, Nuevo Leon, Mexico

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Automotive, ManufacturingIndustries

Requirements

Bachelor’s degree in engineering or related field
Minimum 2 years of experience in quality systems
Experience with ISO 9001/IATF 16949 or VDA
Familiarity with AIAG tools and methodologies
Strong self-motivation and communication skills
Ability to work across all organizational levels
Fluent in English and Spanish

Responsibilities

Develop technical data sheets for purchased products and materials
Support and lead the creation of test methods for Clarios labs
Identify and manage third-party labs for component certification
Participate in supplier selection based on quality criteria
Conduct audits of supplier quality systems, processes, and facilities
Review and approve Supplier PPAPs and related documentation (Control Plans, Capability Studies, FMEAs, Gage R&R, etc.)
Resolve supplier quality issues using structured problem-solving (8D, containment actions)
Facilitate Management Quality Reviews with underperforming suppliers
Monitor corrective actions and track supplier PPMs
Support supplier development and certification renewals (API, Dexson, Nize, etc.)
Perform onsite inspections and sorting of purchased products
Validate packaging for purchased parts and materials
Develop homologation processes for OE customer requirements
Lead continuous improvement and cost-saving projects with suppliers

Skills

ISO 9001

IATF 16949

VDA

APQP

FMEA

PPAP

SPC

PPM

Supplier Audits

Control Plans

Capability Studies

Gage R&R

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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