27 English-speaking jobs in Siena

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.

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.

The Global Study Manager drives clinical operations of assigned studies from Commit to Study Initiation through archiving. Responsibilities include leading the Operational Working Group, crafting delivery plans, ensuring timelines and quality standards are met, and collaborating with the Global Study Lead. The role requires a Bachelor's degree in life sciences, in-depth clinical research experience, strong project management skills, and knowledge of GCPs and ICH guidelines.

Archivist for biotech-pharmaceutical company. Responsible for archiving, classifying, and managing paper and digital documentation. Requires high school diploma and proficiency in Microsoft Office Suite. Previous experience in archiving or document management preferred.

Leads clinical study operations, ensuring delivery to time, quality, and budget standards. Accountable for study deliverables, vendor oversight, and compliance with ICH/GCP guidelines. Requires in-depth clinical research experience, strong project management skills, and excellent stakeholder communication.

Leads the development and execution of regional regulatory strategy for assigned assets, ensuring compliance with global and local requirements. Collaborates with Global Regulatory Lead, Local Operating Company Regulatory Affairs, and regional stakeholders to achieve optimal labeling and regulatory approvals. Provides regulatory expertise and insights to support regional business objectives and contribute to the development of Global Regulatory Strategy.

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. offers internship opportunities in Finance and HR for recent graduates or students seeking professional development. The Finance internship provides hands-on experience in accounting, treasury, consolidation, and controlling. The HR internship offers practical training in personnel administration, recruitment, labor law, and HR operations.

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.

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.

Senior Automation Engineer to lead the resolution of technical challenges and drive the implementation of innovative solutions within a production environment.

Senior System Engineer to manage complex IT/OT infrastructures, resolve advanced technical challenges, and design high-availability solutions.

Drivers will operate client-provided vehicles equipped with mapping equipment to collect street-level data. Requires 5+ years of driving experience, at least 2 years professional driving, and good English. Must be comfortable driving in high-traffic conditions and have familiarity with GPS devices and local roads. Travel and extended assignments are required.

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 seeks a Medical Doctor to serve as Deputy Chief Medical Officer. This role provides medical oversight and leadership for clinical trials, supporting R&D in product development. Responsibilities include developing strategic plans, designing study protocols, supervising pharmacovigilance, and interacting with regulatory and project management teams.

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.

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.

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.

Mechanical Engineer needed for Head Quarter Engineering Team. Manages project development, creates construction drawings, and ensures product compliance with standards. Requires a Mechanical Engineering degree, 2+ years of experience, and proficiency in design programs and Microsoft Office.