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
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
We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension
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
Quality Control Composite Manufacturing Scopo della posizione Verifica e si assicura che la qualità richiesta durante il ciclo produttivo e del prodotto finito rispetti gli standard aziendali definiti, mettendo in atto tutte le azioni necessarie al loro
Overview In this role you will carry out pharmacovigilance (PV) operations for interventional clinical trials, ensuring compliant, high-quality safety data and up-to-date processes. You’ll work with global teams and CROs to support PV requirements across R&D assets.
This is what you will do Carry out pharmacovigilance (PV) operations (OPS) activities in interventional clinical trials sponsored either by GCD or GRD functions by maintaining up-to-date processes for safety-related aspects of interventional clinical trials, to
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you
Deadline for Applications: 24 August 2026, 23:59, Italy time zone Are you an experienced leader with a strong track record of managing scientific functions, shaping strategic priorities and guiding multidisciplinary teams in a complex and evolving
Are you curious and ready to accept a new challenge in your career? Are you eager to join a dynamic company and bring innovation through your work and skills? Prometeia offers you opportunities for growth and
Cellularline Group è, con i marchi Cellularline, Interphone, Nova, Skross, Audio Quality Lab, Music Sound e Coverlab, l’azienda leader nel settore degli accessori per smartphone e tablet. Il Gruppo, fondato a Reggio Emilia nel 1990 e, quotato
Experis è la società IT & Technology del Gruppo Manpower. Le persone e le loro competenze sono il nostro successo e insieme ci poniamo come partner tecnologici dei nostri clienti attraverso servizi e soluzioni. Vogliamo essere
Apply for Medical Assistant - Parma Office at Apex Skin in Parma, EMI, IT. This Full time on site position offers great opportunities for career growth. About Apex Skin We are Apex Skin, and our mission
The Pomology Program at U of I, based at the Parma Research and Extension Center, conducts research and extension to support fruit production systems across Idaho. This position offers hands‑on experience with apples, cherries, almonds, and
The opportunity This role is designed for a strategic builder, integrator, and intrapreneur—someone who will shape market positioning, drive portfolio competitiveness, and influence long‑term business success. As a member of the GPQSS Management Team, you will
This role is designed for a strategic builder, integrator, and intrapreneur—someone who will shape market positioning, drive portfolio competitiveness, and influence long‑term business success. As a member of the GPQSS Management Team, you will own the
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you
Teckal S.p.A., società del Gruppo Rekeep, opera nei servizi energetici con focus sullefficientamento degli edifici Pubblici e Privati. Gestisce lintero ciclo energetico degli immobili: forniture energetiche, conduzione, manutenzione e riqualificazione degli impianti, intervenendo direttamente nelle fasi