Johnson & Johnson Posted September 3, 2026

Quality Assurance Operations 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).

Le attività previste dal ruolo comprendono:

Revisione dei dati prodotti nelle fasi del processo di produzione farmaceutica (Batch Record Review) al fine di verificare la conformità del prodotto ai requisiti normativi e regolamentari in vigore per consentire il rilascio dei lotti sul mercato;

Gestione delle criticità qualitative (Quality Issues) sui lotti farmaceutici prodotti in rispetto delle specifiche e delle procedure vigenti;

Gestire le indagini relative ai problemi di qualità e loro risoluzione con un intervento sul campo volto a proporre azioni correttive e preventive a breve/medio e lungo termine, in collaborazione con gli altri dipartimenti aziendali;

Interazione e collaborazione con i vari dipartimenti aziendali per supportare un processo di revisione impeccabile, con i gruppi internazionali e le affiliate a supporto della gestione delle indagini.

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

Esecuzione e definizione delle necessarie attività di controllo e delle relative procedure operative;

In quest'area valutiamo candidati in possesso dei seguenti requisiti:

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

Esperienza pregressa di almeno 6 mesi in settore farmaceutico o simile (Esperienza pregressa in Quality Assurance è preferita);

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 266 comparable Associate Quality roles across 71 biopharma companies.

266Comparable roles tracked
249Currently active
71Companies hiring similar roles
28Countries represented

Salary context

47 of 266 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 Associate Scientist · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Highest disclosed · Senior Manager, Quality Assurance · Gilead Sciences, Inc. $157,590/yr – $203,940/yr
Peer group range $66,560 – $180,765 (median $153,000)

Where these roles are based

Top locations among the 266 comparable roles

United States90
Germany26
China20
France14
India14
Ireland13

+ 22 more countries

Seniority mix

266 of 266 peers have a known seniority level

Manager164
Intern/Fellow/Postdoc60
Associate42

Therapeutic area mix

0 of 266 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

50%similar
Chiesi Farmaceutici Milano, Italy Manager
Same function Adjacent seniority Same country
50%similar
Boehringer Ingelheim Noventa Padovana, Italy Intern/Fellow/Postdoc
Same function Adjacent seniority Same country
45%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same seniority
45%similar
Novartis Barcelona Gran Vía, Spain Associate
Same function Same seniority
45%similar
RayzeBio, Inc Indianapolis, United States Associate
Same function Same seniority
45%similar
Amgen Technology Pvt Ltd. Hyderabad, India 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.

50%
QA Sterility Assurance Manager, Nerviano Site (Milano, IT)
Chiesi Farmaceutici · Milano, Italy · Manager
Function Therapeutic area Adjacent seniority Country
45%
Advisor, Physicochemical Properties and Compound Quality
Lilly · Indianapolis, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
45%
Associate Scientist I, Quality Control, Isotope Production
RayzeBio, Inc · Indianapolis, United States · Associate
Function Therapeutic area Seniority Country
45%
Associate-QA Compliance
Lilly · Suzhou, Shanghai, China · 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.