21 English-speaking jobs in Siena

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).

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.

The AI Developer will support Sediver's AI initiatives across business and operations. The role focuses on developing, implementing, and deploying AI-powered solutions, particularly leveraging Large Language Models (LLMs) and agent-based systems. The AI Developer will collaborate with IT, business stakeholders, and R&D teams to drive innovation and enhance process efficiency.

Legal Specialist to draft, review, negotiate, and finalize commercial agreements for a retail business. Requires a Law degree, experience in international law firms, and fluency in English.

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

Select by Roast Jobs connects skilled culinary professionals with top-tier hospitality venues across Europe. We are recruiting Sous Chefs for luxury hotels, fine dining restaurants, and Michelin-starred kitchens. As Sous Chef, you will support the Head Chef in managing kitchen operations, ensuring high standards, team coordination, and menu excellence.

MAASI Enterprises seeks final-year students or recent graduates for a paid internship in CSV, QA, Regulatory Affairs, and related fields. Interns will draft technical documentation, execute computerised systems testing, and support clients.

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.

Clinical Data Manager will perform data cleaning, design CRFs, collaborate on database implementation, and prepare data management documentation. Requires a Master's degree in healthcare, 2 years of clinical trial data management experience, and strong organizational and communication skills.

The GMP Sterility Assurance Specialist will contribute to the definition and implementation of Contamination Control strategies, ensuring compliance with GMP regulations. The role involves supporting microbiological risk assessments, environmental monitoring, and the qualification of cleanrooms and critical utilities. The Specialist will also write and review GMP documentation, participate in investigations, and collaborate with various departments to ensure the control of sterile processes.

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.

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.

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.

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.

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

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.

The Computational and Translational Genomics Laboratory (CTGLab) seeks a Postdoctoral Researcher to develop computational methodologies for real-time genomic and epigenomic profiling using Oxford Nanopore Technologies. The successful candidate will design and implement pipelines for long-read sequencing data analysis, integrate multi-omics data, and contribute to personalized treatment strategies for glioblastoma patients.

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.