QA Equipment Validation Specialist
QA Equipment Validation Specialist
QA Equipment Validation Specialist
QA Equipment Validation Specialist
Aenova Holding GmbH
Pharmazeutische Produkte, Arzneimittel
Latina
- Art der Beschäftigung: Vollzeit
- Vor Ort
- Zu den Ersten gehören
QA Equipment Validation Specialist
Über diesen Job
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
Haupt Pharma Latina S.r.l. • Member of the Aenova Group • Strada Statale 156 dei Monti Lepini • 04100 Borgo San Michele LT, Italy