×
Register Here to Apply for Jobs or Post Jobs. X

QA Equipment Validation Specialist

Job in 04100, Latina, Lazio, Italy
Listing for: Altro
Full Time position
Listed on 2026-06-28
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Engineering
  • Pharmaceutical
    Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 40000 - 60000 EUR Yearly EUR 40000.00 60000.00 YEAR
Job Description & How to Apply Below
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.

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.

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).

Note

Please note:

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

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

#J-18808-Ljbffr
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary