d) at Clairo

Zwickau, Saxony, Germany

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Automotive, ManufacturingIndustries

Requirements

Bachelor/Ingenieur oder Staatl. Geprüfter Techniker oder Facharbeiter mit langjähriger Berufserfahrung im Qualitätsmanagement/-wesen
Kenntnisse IATF 16949, FMEA, Produktionslenkungsplan, APQP, PPAP
IT-Affinität (u.a. SQL, Power-BI, Power-Automate)
Kenntnisse Statistikverfahren und -software (z.B. Q-DAS, InfinityQS)
Kenntnisse im Bereich Messmittelkalibrierung
Gute Sprachkenntnisse Deutsch und Englisch

Responsibilities

Qualitätsvorausplanung, z.B. APQP, FMEA, CSR usw
Optimierung der betrieblichen Datenerfassung im Bereich Qualität
Koordination betriebliches Dokumentenmanagement (gelenkte Dokumente)
Dokumentenpflege (Produktionslenkungsplan, Prüfpläne usw.)
Erstellung, Bewertung und Koordination von MSA’s
Durchführung und Bewertung von Prozessfähigkeitsuntersuchungen
Trendverfolgung
Durchführung und Optimierung von Qualitätsauswertungen
Vorbereitung und Koordination von Audits (interne Prozessaudits)
Koordinierung der Messmittelüberwachung

Skills

APQP

FMEA

IATF 16949

SQL

Power BI

Power Automate

Q-DAS

InfinityQS

PPAP

MSA

Produktionslenkungsplan

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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