Now is an amazing time to join Nozomi Networks as we build the future of OT and IoT cybersecurity. We defend some of the world’s largest organizations and critical infrastructure in more than 68 countries and
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
In the role of F&B Coordinator at Grand Hotel Timeo you will provide support to the Food & Beverage Manager and the F&B department in daily administrative and operational activities. This role will contribute to maintaining
Get to know us Ideals is a global B2B SaaS product company recognized as the most highly rated and customer-centric brand in the secure business collaboration market. Trusted by over 2,000,000 users from 300,000 companies globally,
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
NEXTCHEM, a company of the MAIRE Group dedicated to Sustainable Technology Solutions, is seeking a dynamic and innovative Expediter to join our team. The successful candidate will play a crucial role in the development and optimization
Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Principal Regulatory Writer, Global Rare Diseases Chiesi is an international research-focused biopharmaceutical group with 90 years’
Experteer OverviewIn this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and regulatory
OverviewTechnical WriterWe are seeking a highly qualified and motivated Technical Writer to join our team. The ideal candidate will have excellent writing skills and a strong understanding of complex technical topics. The Technical Writer will be responsible for
In this role you will: Plan and create new product-focused technical content for administrators, end-users, and internal employees by collaborating with Nozomi’s cross-functional group of subject-matter experts, including Engineering, Product, Support, and Solution Engineering teams. Help
Chiesi Farmaceutici S.p.A. is seeking a Principal Regulatory Writer for their Global Rare Diseases department in Parma, Italy. This role involves managing regulatory documents for global health authorities, ensuring compliance and quality throughout the drug development lifecycle.The ideal
Experteer Italy seeks a candidate to author and manage regulatory documents that translate data into compliant submissions. This role involves overseeing document development for marketing applications and guiding both external writers and internal experts.The ideal candidate will have a
Chiesi Farmaceutici S.p.A. is looking for a Global Pharmacovigilance Medical Safety Writer in Parma. This temporary position involves developing pharmacovigilance documents, supporting global planning for molecules, and ensuring compliance with safety reporting standards. Ideal candidates should have at
Now is an amazing time to join Nozomi Networks as we build the future of OT and IoT cybersecurity.We defend some of the world’s largest organizations and critical infrastructure in more than 68 countries and we’re
Now is an amazing time to join Nozomi Networks as we build the future of OT and IoT cybersecurity. We defend some of the world’s largest organizations and critical infrastructure in more than 68 countries and
Mission We are looking for a Technical Writer who will be in charge of creating, updating and publishing technical documentation and manuals = shipping with Schneider Electric’s cooling products. The candidate will be part of the Engineering
Global Pharmacovigilance Medical Safety Writer - Temporary Date: 28 Apr 2026 Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Temporary Location: Italy (Parma) with possibility
Overview Technical Writer We are seeking a highly qualified and motivated Technical Writer to join our team. The ideal candidate will have excellent writing skills and a strong understanding of complex technical topics. The Technical Writer will be responsible
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description FSP Senior Regulatory Medical Writer At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission