2 annunci per il ruolo di qa equipment validation specialist - latina, laz (recruiting in corso)

QA Equipment Validation Specialist
Aenova Holding —Latina, Lazio
- Tempo pieno
- Ingegneria
- Sistemi ERP
- Inglese
Qualification / Validation Specialist
Aenova Holding —Latina, Lazio
- Tempo pieno
- Gestionale
- Ingegneria
- Inglese

More jobs to discover

Find similar jobs that you might be interested in.

Qualification / Validation Specialist
Aenova Holding —Latina, Lazio
The purpose of these roles is to ensure the qualification status of the production equipment, QC instrument & equipment and Warehouse through the definition of…
QA Equipment Validation Specialist
Aenova Holding —Latina, Lazio
2–3 years of experience in qualification/validation within pharmaceutical companies. Prepare and maintain validation-related SOPs and policies; assess change…

Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di qa equipment validation specialist nella seguente località: latina, laz

Accedendo al tuo account, accetti i Termini di Servizio di SimplyHired e acconsenti alle nostre Norme sui Cookie e sulla Privacy.

QA Equipment Validation Specialist

Aenova Holding -
Latina, Lazio

Candidati adesso

Dettagli della posizione

Tempo pieno

Qualifiche

Ingegneria
Sistemi ERP
Inglese
Microsoft Office
IT
Produzione
Italiano

Descrizione completa della posizione

for the site Borgo San Michele LT, Italy

Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.

Your key responsibilities

Provide expertise in validation, ensuring compliance with industry regulations, guidelines, and trends.
Review and approve qualification and validation protocols, reports, and related documentation, including premises, equipment, and utilities.
Prepare and maintain validation-related SOPs and policies; assess change controls for validation impact.
Troubleshoot validation deviations, participate in revalidation programs, and support cross-functional projects as QA validation representative.
Maintain organization and archival of all validation and qualification documentation.
Act as point of contact for customers during audits, inspections, and validation-related discussions, ensuring professional and solution-oriented communication.

Your profile

Degree in a scientific or engineering discipline (e.g., Chemistry, Biotechnology, Engineering, Pharmaceutical Chemistry).
Previous experience in the pharmaceutical industry is highly valued and essential for this role.
2–3 years of experience in qualification/validation within pharmaceutical companies.
Experience in sterile manufacturing (Fill & Finish) is a strong advantage.
In-depth knowledge of GMP, GAMP, and major international standards (FDA, EMA).
Strong technical documentation skills, attention to detail, and ability to work independently.
Excellent interpersonal and communication skills, with confidence in direct customer interactions.
Team-oriented mindset and strong IT skills (MS Office, ERP, document management systems).

Please note: Applications must be submitted in English. Applications in Italian or any other language will not be considered.

Your motivation

Are you looking for new challenges in a highly competitive environment? And you want to tackle them creatively and on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions rather than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!

If you have any questions, I - Lukas Rödder / Human Resources - will be happy to help you: +49 151 16260074

Online seit: 08.02.2026

Beschäftigungsverhältnis
Vollzeit
Unternehmen
Haupt Pharma Latina S.r.l.
Bereich
Qualität

Kontakt

Haupt Pharma Latina S.r.l. • Member of the Aenova Group • Strada Statale 156 dei Monti Lepini • 04100 Borgo San Michele LT‚ Italy

Candidati adesso

Perfeziona la tua ricerca

qa equipment validation specialist offerte - latina, laz

QA Equipment Validation Specialist

Qualification / Validation Specialist

More jobs to discover

Voglio ricevere gli ultimi avvisi Job Alert per il ruolo di qa equipment validation specialist nella seguente località: latina, laz

Your key responsibilities

Your profile

Please note: Applications must be submitted in English. Applications in Italian or any other language will not be considered.

Your motivation

Strumenti per chi cerca lavoro

Strumenti Aziende

Visualizza

Resta in contatto