QA Associate

jj· 7175-Janssen Cilag S.p.A. Legal Entity
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Full timeHybrid Work7175-Janssen Cilag S.p.A. Legal Entity

About this role

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Business Enablement/Support

All Job Posting Locations:

Latina, Italy

Job Description:

A proposito di Innovative Medicine

La nostra esperienza in Innovative Medicine è ispirata dai pazienti, la cui conoscenza alimenta i nostri progressi scientifici. I visionari come te lavorano in team che salvano vite sviluppando le cure del domani.

Unisciti a noi nello sviluppo di trattamenti, nella ricerca di cure e nel pionieristico percorso dal laboratorio alla vita, sostenendo i pazienti in ogni fase del percorso.

Per ulteriori informazioni, visitare il sito Web https://www.jnj.com/innovative-medicine

Stiamo cercando il miglior talento nel ruolo di Quality Assurance Associate, Master Data, basato a Latina.

Scopo:

Per il sito produttivo di Borgo San Michele (Latina) ricerchiamo candidati da inserire a TEMPO DETERMINATO per 12 MESI presso il Dipartimento Quality che ha la responsabilitĂ  di assicurare la conformitĂ  del prodotto alle norme e alle specifiche nazionali ed internazionali che regolano il settore farmaceutico sia dal punto di vista del controllo sul prodotto stesso sia dal punto di vista della documentazione ad esso legata.

Nello specifico, la risorsa scelta sarĂ  inserita nell'area Quality Assurance, che ha la responsabilitĂ  di assicurare, attraverso la verifica del rispetto di procedure operative standard e mediante opportuni strumenti, che la qualitĂ  del prodotto sia conforme alle specifiche e normative vigenti (GMP).

ResponsabilitĂ :

  • Approvare la documentazione di produzione (Master Batch Record e ricette) e dell’anagrafica dei materiali, degli equipment e delle risorse (Master Data), assicurando il rispetto dei tempi e la qualitĂ  dell’intero processo, monitorandone il cycle time e coordinandosi con il gruppo globale per l’approvazione dei Master Data.

  • Controllare e garantire la gestione dei dati critici relativi ai Master Data, in accordo alle GMP ed ai requisiti di qualitĂ  e compliance definiti dalle procedure aziendali assicurandone la relativa approvazione.

  • Collaborare e partecipare come riferimento Quality per il sito ai team crossfunzionali di progetto (New Product Introduction, Technology Transfer, Technical Launch, Validation Process) al fine di assicurare le date di lancio dei prodotti sul mercato.

  • Svolgere attivitĂ  di supporto nei processi di qualitĂ , inclusa la gestione delle non conformtĂ , il monitoraggio dell’implementazione di azioni correttive/preventive e richieste di cambiamento (Change Control) legate ai progetti assegnati.

  • Gestire la risoluzione delle problematiche dei diversi reparti dello stabilimento in relazione alla gestione dei prodotti, dei processi, di equipment/facilities/utilities al fine di assicurare la qualitĂ , sicurezza ed efficacia dei prodotti.

  • Agire come rappresentante QA in progetti aziendali al fine di curarne gli aspetti di qualitĂ .

  • Garantire un’efficace assistenza al Servizio di Produzione, fornendo le soluzioni necessarie al superamento di situazioni critiche.

 

Qualifiche / Requisiti:

  • Laurea magistrale in Chimica e Tecnologie Farmaceutiche, Farmacia, Chimica o Biologia; Ingegneria; Informatica

  • Esperienza di 12 mesi in settore farmaceutico o simile;

  • Ottima conoscenza della lingua inglese;

  • Buona conoscenza del pacchetto office.

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here’s what you can expect:

  • Application review: We’ll carefully review your CV to see how your skills and experience align with the role.

  • Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.

  • Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.

  • Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.

                                                                                                                                         

Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA

#LI-Hybrid

 

 

Required Skills:

 

 

Preferred Skills:

Accountability, Administrative Support, Compliance Management, Detail-Oriented, Document Management, Execution Focus, Goal Attainment, Human-Centered Design, Internal Controls, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Report Writing

  

 

The anticipated base pay range for this position is:

€29,800.00 - €48,530.00

 

 

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

 

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

 

 

Frequently Asked Questions

Is the salary disclosed for the QA Associate position at jj?
The salary for this QA Associate role at jj is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the QA Associate position at jj located?
This QA Associate role at jj is based in Latina, Italy. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the QA Associate role at jj full-time or part-time?
This is listed as a Full time position. It is posted as a QA Associate role in the 7175-Janssen Cilag S.p.A. Legal Entity department at jj.
Which team or department does the QA Associate at jj belong to?
This QA Associate position is part of the 7175-Janssen Cilag S.p.A. Legal Entity department at jj. See the full job description for more information about the team structure and responsibilities.
How do I apply for the QA Associate position at jj?
Click the "Apply Now" button on this page. You will be redirected to jj's official application portal hosted on workday where you can submit your application directly.

You'll be redirected to jj's official application page on Workday.