29 English-speaking jobs in Siena

The Supplier Quality Engineer Intern supports supplier quality activities, including monitoring performance, assisting with supplier assessments, and contributing to supplier readiness during launch phases.

As a Beauty Advisor, you will greet customers, provide personalized consultations, and support store management in achieving objectives. Previous experience in retail sales and knowledge of key commerce KPIs are required.

Senior Biostatistician to contribute to study design, statistical analysis planning, and clinical trial execution. Requires a degree in Biostatistics, Statistics, Mathematics, or a related field, strong statistical background, and proficiency in SAS.

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.

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.

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

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.

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.

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 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.

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

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.

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.

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.