13 ott - Latina
Aenova Group
for the site Borgo San Michele LT, Italy
Si candidi ora: legga i dettagli del lavoro scorrendo verso il basso. Verifichi di possedere le competenze necessarie prima di inviare la candidatura.
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 environ
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