Johnson & Johnson Posted September 3, 2026

Quality Assurance Associate

Latina, Italy Full time
Quality Associate
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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 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 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 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 Assurance, che ha la responsabilità di assicurare, attraverso la verifica del rispetto di procedure operative standard e mediante opportuni strumenti, che la qualità del prodotto sia conforme alle specifiche e normative vigenti (GMP).

La persona ricercata sarà responsabile delle seguenti attività:

Gestione di reclami e delle criticità qualitative (Non Conformance) sui lotti farmaceutici prodotti, il rispetto delle specifiche e delle procedure vigenti;

Gestire reclami e indagini relative a problemi di qualità e volte ad identificare adeguate azioni correttive e preventive a breve/medio e lungo termine, in collaborazione con gli altri dipartimenti aziendali;

Collaborazione diretta con la farmacovigilanza, con i gruppi internazionali e con le affiliate a supporto della gestione dei reclami e delle indagini;

Identificare opportunità di miglioramento e verificare la correttezza delle operazioni di produzione più critiche, attraverso una presenza costante in produzione.

Qualifiche / Requisiti:

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

Esperienza pregressa di almeno 24 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.

Job details

Seniority
Associate
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 216 comparable Associate Quality roles across 76 biopharma companies.

216Comparable roles tracked
204Currently active
76Companies hiring similar roles
33Countries represented

Salary context

35 of 216 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Associate Scientist- Overnight Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Highest disclosed · Senior Manager, Quality Assurance · Gilead Sciences, Inc. $157,590/yr – $203,940/yr
Peer group range $75,920 – $180,765 (median $163,000)

Where these roles are based

Top locations among the 216 comparable roles

United States64
China22
Ireland16
India15
Japan12
Belgium8

+ 27 more countries

Seniority mix

216 of 216 peers have a known seniority level

Manager182
Associate22
Intern/Fellow/Postdoc12

Therapeutic area mix

1 of 216 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

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.

60%similar
Lilly SESTO FIORENTINO, Firenze, Italy Associate
Same function Same seniority Same country
50%similar
AbbVie Campoverde, Lazio Manager
Same function Adjacent seniority Same country
50%similar
Chiesi Farmaceutici Parma, Italy Manager
Same function Adjacent seniority Same country
50%similar
Chiesi Farmaceutici Milano, Italy Manager
Same function Adjacent seniority Same country
50%similar
Johnson & Johnson Latina, Italy Manager
Same function Adjacent seniority Same country
45%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority

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.

60%
Quality Assurance Associate - Fixed Term Contract (12 months)
Lilly · SESTO FIORENTINO, Firenze, Italy · Associate
Function Therapeutic area Seniority Country
50%
QA Sterility Assurance Manager, Nerviano Site (Milano, IT)
Chiesi Farmaceutici · Milano, Italy · Manager
Function Therapeutic area Adjacent seniority Country
45%
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis · Barcelona Gran Vía, Spain · Associate
Function Therapeutic area Seniority Country
45%
Associate Product Quality - Data Verification
Amgen Technology Pvt Ltd. · Hyderabad, India · Associate
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.