Analista di laboratorio - Tempo determinato 12 mesi

Benefits

Parental leave

12 weeks From the posting source

Non-birth-parent leave

12 weeks From the posting source

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Source-linked checked May 7, 2026

Salary

Not verified

401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Role

Seniority

Mid From the posting source

Schedule

Shift type

Not verified

Weekend work

Not verified

Company

Equity

Offered Verified - SEC 10-K source

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Analista di laboratorio - Tempo determinato 12 mesi Campoverde, Lazio, Italy Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description: Intraprendere una carriera in AbbVie significa affinare le proprie capacità, creare connessioni profonde e acquisire esperienza facendo la differenza. Attualmente AbbVie ricerca, per la sede di Campoverde di Aprilia (LT), una figura di QC Analyst da inserire con un contratto a tempo determinato di 12 mesi, con le seguenti responsabilità: Job Responsibilities: Documentare secondo le procedure, negli opportuni registri e/o nei sistemi informatici la ricezione dei campioni in laboratorio; Eseguire l'analisi secondo la Specifica e seguendo attentamente ed esattamente la metodica descritta nei metodi analitici in vigore garantendo la compliance rispetto al Data Integrity attraverso la corretta applicazione delle GMP, policies e procedure Verificare al termine dell'analisi la conformità del System Suitability, segnalando immediatamente ogni failure al lab shift supervisor/lab program coordinator del laboratorio in cui opera garantendo inoltre un adeguato passaggio di consegne . Registrare tutte le informazioni e i dati analitici sui Notebook di laboratorio e nei sistemi informatici previsti da procedura (LIMS, Empower...), avendo verificato la correttezza

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