28 English-speaking jobs in Siena

Archivist for Protected Categories Law 68/99 needed. Responsibilities include archiving, document management, and operational support for technical and scientific functions. Requires high school diploma, Microsoft Office proficiency, and experience in archiving, secretarial, or document management.

Storage Solutions Market Expert to define value proposition, enable sales teams, and lead technical exchanges with IT decision makers. Requires 5+ years of experience in storage solutions architecture and pre-sales, mastery of storage protocols and networking, and deep understanding of storage technologies. Proven track record with SAN and NAS deployments in large-scale enterprise environments.

HR Generalist to support personnel administration, recruitment, onboarding, attendance management, HR reporting, and employee support.

Cambrex Profarmaco Milano seeks a Computer Science/Engineering intern to develop an AI-powered HPLC recommendation engine. The intern will design a knowledge database, develop predictive models, and build a recommendation system using proprietary pharmaceutical data.

Philogen, a Swiss-Italian biotechnology company, seeks a Human Resources Intern to support daily HR operations, recruitment, and personnel administration. The intern will assist with tasks such as drafting job advertisements, managing attendance records, and analyzing personnel costs.

Recent graduates in Biology, Biotechnology, Chemistry, or related fields sought for a 6-month GMP internship. Support GMP operations in CMC Production, Quality Control, or CMC Quality Assurance.

Develop and extend the backend of an Energy Management System in a distributed edge/cloud environment. Design scalable architectures using Go, primarily for edge devices and cloud components. Develop cloud data interfaces for reliable data exchange between edge devices and cloud services. Plan, implement, and maintain database solutions, especially with PostgreSQL. Integrate hardware components into the Energy Management System.

Develop and extend the backend of an Energy Management System in a distributed edge/cloud environment. Design scalable architectures using Go, develop cloud data interfaces, and integrate hardware components.

Leads the design and delivery of complex initiatives to enhance Drug Development and Supply (DDS) performance and organizational readiness for change. Serves as an integrator across functions, ensuring programs and innovations are translated into tangible impact. Drives process standardization, optimization, and embedding, ensuring consistency and high-quality execution across DDS.

Philogen S.p.A. seeks recent graduates in Biology, Biotechnology, Chemistry, or related fields for a 6-month GMP internship in CMC Production, Quality Control, or CMC Quality Assurance. Interns will support GMP operations, participate in daily activities, and assist in monitoring processes and documentation.

Philogen S.p.A. seeks an Archivist belonging to Protected Categories (Law 68/99) to manage paper and digital documentation, ensuring traceability and compliance with company procedures.

Leads a global oncology labelling team, ensuring compliance with regulatory requirements and developing clear, compliant product labels. Manages the GSK labelling process from early development through lifecycle management. Provides strategic direction for labelling governance and advises on labelling issues to senior management.

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

Executive Assistant to support the Board of Directors and Senior Management. Responsibilities include calendar management, meeting scheduling, document preparation, and communication coordination. Requires a high school diploma or university degree, previous executive-level administrative experience, and fluency in English.

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.

Finance Intern to support accounting, consolidation, and controlling activities at a biotechnology company.

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).

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.

Philogen seeks a Deputy Chief Medical Officer to provide medical oversight and leadership for clinical trials. The role supports the development of strategic plans, designs study protocols, and supervises pharmacovigilance. Requires a medical degree and 5+ years of clinical development experience in a pharmaceutical company.

GMP Quality Assurance Specialist will write, review, and approve documents, revise batch records, and manage GMP QA operations. Requires a scientific background, at least three years of QA experience, and strong knowledge of GMP and global quality standards.