31 English-speaking jobs in Siena

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.

Biochemical Quality Control Supervisor will oversee laboratory functions, ensure compliance with GMP regulations, and support analytical method development. Requires a strong scientific background, GMP knowledge, and expertise in chromatographic and biological testing techniques.

IT Specialist to support IT infrastructure management, projects, and help desk support. Requires 1-3 years of experience in enterprise IT asset management and AI/ML project deployment. Proficiency in Windows, macOS, Active Directory, M365, and SQL.

Bioanalytical Scientist to perform bioanalytical testing, method development, and data analysis in a preclinical and clinical setting. Requires a Master's Degree in a relevant field and hands-on experience with mass spectrometry.

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 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.

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.

The Quality Control Release & Stability Testing Director is responsible for end-to-end oversight of QC release and stability testing activities for clinical products. This leader will define strategy, build and lead teams, drive technical and regulatory excellence, and partner across functions to ensure timely, compliant product release and a robust stability program.

Leads strategic initiatives to advance process and product understanding through analytical techniques like mass spectrometry, NMR, and microscopy. Oversees development and implementation of extended characterization platforms to support drug discovery, development, and manufacturing. Builds, mentors, and leads a team of scientists, fostering collaboration and innovation. Partners with cross-functional teams to align characterization efforts with organizational goals.

As a Specialist, you will manage a product category, facilitate communication, support managers, and monitor team KPIs. You will coordinate activities, manage stock, implement procedures, and train new hires.

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. Experience with larger vehicles is preferred. Travel and extended assignments are required.

Experienced teacher of IBDP (SL/HL) and MYP Chemistry needed for an International school in Italy. Must have experience teaching both IB MYP and DP, and be able to plan and deliver curriculum for IBDP Chemistry HL/SL and BMYP G10 & 11 Chemistry.

Experienced teacher of IBDP (SL/HL) and MYP Chemistry sought for International school in Italy. Must have experience teaching both IB MYP and DP, with ability to teach MYP maths desired.

Leads and coordinates clinical and evidence generation studies from planning through close-out. Works with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant. Monitors study conduct and progress, identifies and resolves risks/issues, and drafts and reviews key clinical documents. Provides country-level oversight, manages study communications, and oversees clinical supply and investigational product delivery. Ensures eTMF inspection readiness and manages study budget and expenses. Contributes to Study Leadership and Central Study Teams.

Store Manager will lead a team in achieving financial targets, coordinating store activities, managing inventory, and implementing company policies.

Provides Quality Leadership for network strategy projects that strengthen the supply network. Works with cross-functional partners to define and deliver network programs. Ensures on-time delivery of strategy assessments and implementation requirements. Designs and implements quality standards, quality agreements, and oversight models for third-party suppliers. Coordinates risk assessments, remediation plans, and CAPA oversight. Drives data-led decision making using quality metrics and trends. Leads cross-functional working groups and provides updates to senior governance forums. Develops capability through coaching, training, and sharing best practice.

Manages serialization and packaging processes for pharmaceutical products, ensuring compliance with international regulations.

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.

The GMP Quality Assurance Specialist will contribute to quality policies in support of Philogen's Quality System. Responsibilities include writing, reviewing, and approving documents; revising batch records; managing GMP QA operations; identifying improvements; implementing action plans; developing quality strategies; and conducting risk assessments.

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