25 security manager italy English-speaking jobs in Siena

Italy is seeking a Construction Manager to support a high-profile hospitality project in Tuscany. ... About The Role Job title : Construction Manager | Freelance Location : Siena, Tuscany Currie & Brown

The international manufacturing group has production facilities in Italy, Czech Republic, China and the ... United States, additional sales offices and warehouses in Brazil, Canada, Italy, Saudi Arabia and France ... AI Governance: Support the security and compliance team in enforcing AI governance — EU AI Act, GDPR, ... Responsible AI Awareness of EU AI Act, GDPR, ISO 27001 and NIS2 Model bias and fairness considerations AI security

to the Data Manager Coordinator. ... Philogen S.p.A. would like to hire a highly motivated and qualified Clinical Data Manager who will report

Leads regional regulatory strategy and execution for assigned assets, aligning with global goals and regional regulations. Serves as the regional single point of contact for regulatory matters, ensuring alignment with global and local teams.

Provide medical oversight and strategic leadership for clinical development across the company's portfolio. Shape study designs, regulatory submissions, and safety oversight while coordinating with regulatory bodies and clinical partners.

Lead a global oncology labeling team, shaping compliant product labels for patient care and product success. Drive regulatory-aligned labeling from development to early lifecycle management, collaborating with R&D, Safety, Regulatory, and Commercial teams.

Leads regional regulatory strategy development and execution for assigned assets, aligning with global plans and local requirements. Collaborates with global and local teams to optimize timing and labeling for multiple markets.

looking for a " GMP Sterility Assurance Specialist/Expert " who will report to the GMP Quality Assurance Manager

and basic upkeep Research and identify safe local parking locations to ensure vehicle and equipment security

Sales Manager for the Fitness Industry will generate leads, manage sales procedures, and onboard new members. Reports to the Director of Sales and Marketing. Requires 3 years of sales experience.

motivated and qualified "GMP Quality Assurance Specialist” who will report to the GMP Quality Assurance Manager

Overview The Computational and Translational Genomics Laboratory (CTGLab) at IIT-CNR, Pisa-Siena, Italy ... Duration : 1 year (renewable) Project : TRANSCAN-3 SeqPerGlio Location : CTGLab, IIT-CNR, Pisa-Siena, Italy

developed at Philochem are subsequently manufactured at Philogen’s authorized GMP facilities in Siena (Italy

Job location Sovicille, Siena, Italy On-site position.

Process & Computer System Validation Specialist (GCP) will validate and maintain computerized systems ensuring compliance with GMP/GCP regulations. The role requires 2+ years of pharmaceutical experience, knowledge of computerized systems lifecycle, and regulatory frameworks (FDA 21 CFR Part 11, EU Annex 11, ISPE GAMP).

Freelance Data Engineer to join a small team focused on internal process optimization using AI. Responsibilities include data lifecycle management, building AI-driven workflows, and collaborating on dashboard development. Requires experience with AWS (S3, Redshift), dbt, ETL/ELT, and strong analytical skills.

Human Resources Assistant to support daily HR operations and administrative tasks, including recruitment, personnel documentation, and reporting.

Develop on-premise business in central-southern Tuscany, showcasing the Red Bull brand in cafes, bars, clubs, and events. Build relationships with customers and influencers, and execute sales and marketing strategies.

Qualification & Validation Specialist will prepare and verify qualification and validation documents, draft validation study protocols and reports, and execute qualification protocols and tests. Requires a degree in a relevant field, 3-4 years of pharmaceutical industry experience, and knowledge of GMP, risk-based methodologies, and validation procedures.

Philogen S.p.A. seeks a Medical Advisor to support the management and development of clinical trials in oncology and rheumatology. Responsibilities include contributing to trial design, execution, and analysis, providing expert guidance, and interacting with investigators and regulatory authorities.