Sterility Assurance Specialist
Pubblicato il 10-10-2026 - Aenova Group in Latina
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
Support and oversee Sterility Assurance and aseptic processing activities within sterile manufacturing areas, including APS.
Collaborate with Production, Engineering & Maintenance, MS&T;, Validation and Quality Assurance to identify, assess and mitigate microbiological contamination risks.
Support the definition and implementation of contamination control requirements for sterile operations, qualification and validation activities.
Support deviation investigations, root cause analysis and CAPA definition related to sterility assurance and microbiological events.
Support the implementation, maintenance and periodic review of the Contamination Control Strategy (CCS).
Provide Sterility Assurance expertise during regulatory inspections, customer audits and corporate assessments.
Support technology transfer,
qualification/validation and continuous improvement projects within sterile manufacturing.
Your profile
University degree in a scientific discipline (Biology, Biotechnology, Pharmaceutical Chemistry and Technology, Pharmacy, Chemistry or related fields); Master's degree preferred.
At least 3 years of relevant experience in Sterility Assurance, Microbiology, Quality or Manufacturing within a sterile pharmaceutical environment.
Good knowledge of GMP and EU GMP Annex 1; knowledge of FDA requirements is considered an advantage.
Experience or solid knowledge of aseptic processing, APS and contamination control principles.
Knowledge of Contamination Control Strategy principles.
Good written and spoken English.
Strong analytical, communication and cross-functional collaboration skills.
Experience with cleanroom qualification, technology transfer, environmental monitoring and electronic quality systems is considered a plus.
Annual salary range: EUR ***************
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!
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