Johnson & Johnson Posted August 25, 2026

QC Data reviewer

Latina, Italy Full time

Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 Control

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 QC Data Reviewer - Laboratorio Chimico basato a Latina.

Scopo:

Per il sito produttivo di Borgo San Michele (Latina) ricerchiamo persone in possesso di laurea in discipline scientifiche da inserire a TEMPO DETERMINATO di 12 MESI presso il DIPARTIMENTO QUALITY che ha la responsabilità di assicurare la conformità 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 sarà inserita nell'area QUALITY CONTROL come QC Data Reviewer, che ha la responsabilità di certificare la conformità alle specifiche richieste delle materie prime, del prodotto intermedio/finito e dell'ambiente di produzione.

In particolare, la risorsa scelta sarà inserita all'interno del Laboratorio Chimico e si occuperà di:

Garantire l’aderenza alle norme GMP e alle buone norme di laboratorio (GLP), revisionando la documentazione prodotta, secondo le metodologie definite, al fine di verificare la rispondenza agli standard qualitativi.

Contribuire alla predisposizione di tecniche analitiche ed alla realizzazione di specifici progetti sotto la supervisione del Responsabile del Laboratorio collaborando alla risoluzione dei problemi inerenti.

Garantire l’esecuzione corretta dei test di laboratorio attraverso lo studio dei principi elementari di teoria applicata, lo sviluppo dei calcoli numerici necessari nel corso del trattamento dei dati, proponendo idee e suggerimenti frutto delle proprie osservazioni e conclusioni.

Collaborare insieme al responsabile del laboratorio nella risoluzione delle problematiche analitiche inerenti la sua area di lavoro.

Applicare il continuous improvement sui flussi che impattano il Controllo Qualità allo scopo di identificare aree di miglioramento e opportunità di ottimizzazione dei costi.

Supportare l’inserimento dei colleghi nell’addestramento al ruolo assegnato loro attraverso la funzione di trainer.

Assicurare la revisione della documentazione dei test analitici

Contattare e coordinare i rapporti con eventuali laboratori esterni, per l’effettuazione delle analisi e per la risoluzione di eventuali problematiche analitiche relative alle attività svolte.

Assicurare la corretta gestione dei risultati analitici, verificando l’accettabilità dei risultati e valutando eventuali OOS, OOT ed eventi di laboratorio e garantendo sempre l’integrità dei dati.

Qualifiche / Requisiti:

Laurea in Chimica, Farmacia o CTF;

Ottima conoscenza delle GMP, GDP, GLP e delle norme di sicurezza nei laboratori;

Esperienza in qualità di tecnico di laboratorio o ruolo analogo maggiore di 6 mesi in campo chimico e/o farmaceutico;

Buona conoscenza della lingua inglese (livello B1 o superiore)

Ottime capacità comunicative e di lavorare in team;

Ottime capacità organizzative e orientamento al risultato.

È valutata positivamente una esperienza pregressa nell’ambito di laboratorio chimico QC.

Per questa posizione si offre contratto a tempo determinato di 12 mesi.

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-Onsite

Required Skills:

Preferred Skills:

Accountability, Administrative Support, Compliance Management, Controls Compliance, Execution Focus, ISO 9001, Persistence and Tenacity, Process Oriented, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Report Writing, Teamwork, Technologically Savvy

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.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Latina, Italy
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 989 comparable Quality roles across 117 biopharma companies.

989Comparable roles tracked
898Currently active
117Companies hiring similar roles
50Countries represented

Salary context

202 of 989 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Technician-QC Laboratory · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · AVP, External Quality · Merck $282,200/yr – $444,200/yr
Peer group range $43,753 – $363,200 (median $140,000)

Where these roles are based

Top locations among the 989 comparable roles

United States344
China56
India53
Ireland50
Japan41
Belgium41

+ 44 more countries

Seniority mix

471 of 989 peers have a known seniority level

Manager171
Senior145
Associate Director43
Director38
Associate30
Principal22
Senior Director15
Intern/Fellow/Postdoc4
Executive/VP3

Therapeutic area mix

2 of 989 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Novartis Ivrea, Italy
Same function Same country
40%similar
Lilly SESTO FIORENTINO, Firenze, Italy Associate
Same function Same country
40%similar
AbbVie Campoverde, Lazio Manager
Same function Same country
40%similar
Johnson & Johnson Latina, Italy
Same function Same country
25%similar
Lilly Lebanon, Indiana, United States of America Principal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Qualified Person (QP)
Novartis · Ivrea, Italy · Seniority not listed
Function Therapeutic area Seniority Country
40%
Complaint Quality Approver
Johnson & Johnson · Latina, Italy · Seniority not listed
Function Therapeutic area Seniority Country
25%
Principal Scientist GMP Microbiology Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Principal
Function Therapeutic area Seniority Country
25%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.