Quality Manager at Clairo

Yuma, Arizona, 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

ManufacturingIndustries

Requirements

Bachelor of Science degree in Engineering Technology or related field
Minimum 5 years’ experience in a manufacturing environment
Excellent verbal and written communication skills; ability to present clear and concise information to varied levels within the organization
Must complete Six Sigma training and certification (if not already certified) – company-provided
Certified Black Belt preferred

Responsibilities

Assures QS and ISO requirements are met. Acts as the Plant representative during audits
Manages and directs the activities of the Plant Quality Technicians
Manages Quality Assurance Systems, to include the maintenance of warranty data, in-plant scrap data, compliance data, SNRs, customer concerns, etc. Assures accurate records are maintained for internal and external quality costs. Assure customer expectations are met
Administers and signs off on existing/new process specifications (SCO/DCO system, Control Plan)
Provides technical support to customers and suppliers regarding the resolution of quality of product liability issues
Ensure that the quality management system is maintained and its effectiveness/efficiency is continuously improved, and that the system always complies with the requirements of the current version of the ISO 9001/IATF 16949 specifications

Skills

ISO 9001

IATF 16949

Six Sigma

Quality Assurance

Quality Management Systems

Audits

Process Specifications

Control Plans

Warranty Data

Scrap Data

Customer Concerns

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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