1576 English-speaking jobs in Tuscany

  • Borgo Santo Pietro Lifestyle Group
  • Florence
  • March 6
The Baker/Pastry Chef de Partie will manage a section of pastry and bakery operations, ensuring high-quality production, assisting with recipe execution and innovation, and guiding junior staff.
  • Borgo Santo Pietro Lifestyle Group
  • Siena
  • March 6
The Baker/Pastry Chef de Partie will prepare, bake, and present pastries, breads, desserts, and other baked goods. They will manage inventory, collaborate with the Executive Pastry Chef, and contribute to menu development. Minimum 2 years of experience in pastry or bakery roles is required.
  • Conti di San Bonifacio Wine Resort
  • Florence
  • March 6
Sous Chef to support daily kitchen operations, lead staff, and ensure consistent food quality and presentation. Collaborate on menu execution with a focus on wine pairings and seasonal products. Minimum 4 years of professional culinary experience required.
  • Planckian
  • Florence
  • March 6
Quantum Measurement Engineer will design, implement, and optimize qubit readout and control chains for superconducting quantum processors. Responsibilities include developing measurement protocols, optimizing signal-to-noise ratio, and collaborating with cross-functional teams.
  • Garmin Italy Technologies
  • Florence
  • March 6
Lead Engineer will design, develop, and implement complex cloud-based applications using Java and related technologies. Responsibilities include leading architecture, mentoring team members, and collaborating with other Garmin associates. Requires a Bachelor's Degree in a technical discipline or equivalent experience and a minimum of 8 years of experience developing with Java and related frameworks.
  • Garmin Italy Technologies
  • Florence
  • March 6
Develop and maintain mobile applications using Java/Kotlin/JNI (Android) and Objective-C/Swift (iOS). Design and develop complex C++ software for Garmin's marine mobile solutions. Collaborate with team members on code reviews and problem-solving.
  • Philogen S.p.A.
  • Florence
  • March 6
Senior Director, Regulatory Affairs will develop and execute regulatory strategies for clinical development programs and product lifecycle management. The role involves leading submissions to global regulatory authorities, ensuring regulatory compliance, and collaborating with cross-functional teams.
  • GrantSpider
  • Siena
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Florence
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Prato
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Lucca
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Arezzo
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Pisa
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Livorno
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • GrantSpider
  • Pistoia
  • March 6
Freelance Grant Consultant needed to support EU funding proposals (Horizon Europe, ERC, EIC). Experience with proposal writing, structuring, and coordinating partner contributions required.
  • Pivotal
  • Pisa
  • March 6
Experienced Clinical Research Associate (CRA/SCRA) needed for multi-national projects. Responsibilities include site monitoring, regulatory approvals, quality evaluations, and study progress management. Requires a life science degree, 2+ years of on-site monitoring experience, and knowledge of GCP and ICH guidelines. Must be fluent in English and have strong communication and problem-solving skills.
  • Pivotal
  • Siena
  • March 6
Experienced Clinical Research Associate (CRA/SCRA) needed for multi-national projects. Responsibilities include site monitoring, regulatory approvals, quality evaluations, and study progress management. Requires a life science degree, 2+ years of on-site monitoring experience, and knowledge of GCP and ICH guidelines. Must be fluent in English and have strong communication and problem-solving skills.
  • Pivotal
  • Livorno
  • March 6
Experienced Clinical Research Associate (CRA/SCRA) needed for multi-national projects. Responsibilities include site monitoring, regulatory approvals, quality evaluations, and study progress management. Requires a life science degree, 2+ years of on-site monitoring experience, and knowledge of GCP and ICH guidelines. Must be fluent in English and have strong communication and problem-solving skills.
  • Pivotal
  • Prato
  • March 6
Experienced Clinical Research Associate (CRA/SCRA) needed for multi-national projects. Responsibilities include site monitoring, regulatory approvals, quality evaluations, and study progress management. Requires a life science degree, 2+ years of on-site monitoring experience, and knowledge of GCP and ICH guidelines. Must be fluent in English and have strong communication and problem-solving skills.
  • Pivotal
  • Lucca
  • March 6
Experienced Clinical Research Associate (CRA/SCRA) needed for multi-national projects. Responsibilities include site monitoring, regulatory approvals, quality evaluations, and study progress management. Requires a life science degree, 2+ years of on-site monitoring experience, and knowledge of GCP and ICH guidelines. Must be fluent in English and have strong communication and problem-solving skills.
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