31 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.

Senior Business Analyst with 10+ years of banking experience and 5+ years of Hogan CAMSII (Issuing) expertise. Leads project teams through the software development lifecycle, from requirements gathering to client acceptance testing.

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.

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.

Provides expert guidance on clinical trial design and execution in oncology and rheumatology. Monitors efficacy and safety, reviews regulatory documents, and collaborates with cross-functional teams.

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.

Currie & Brown Italy seeks a freelance Construction Manager for a high-profile hospitality project in Tuscany. Requires a degree in a relevant field, 5+ years managing construction projects, and experience with permitting processes.

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.

Drive sales of digital dental equipment, including imaging systems and CAD/CAM technology. Develop sales strategies, engage with dental professionals, and customize solutions to meet customer needs. Manage the sales process and provide product training.

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.

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.

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.

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.

As a Store Manager, you will lead the Siena team to achieve financial targets, coordinate store activities, manage the P&L statement, and analyze customer behavior. You will also oversee stock management, implement company procedures, and manage a team of Sephora Specialists.

Manages floor operations for one or more product categories (makeup, skincare, fragrance, Sephora Collection). Supports Store Manager and Beauty Advisor team, analyzes KPIs, and coordinates commercial activities. Implements company procedures and trains new hires. Requires 3-4 years of experience in similar retail roles.