Regulatory Affairs Specialist – Global Submissions

KEY RESPONSIBILITIESRedigere, aggiornare e gestire la documentazione regolatoria necessaria per lo sviluppo e la registrazione di medicinali ad uso umano in diverse aree geografiche, collaborando con altre funzioni aziendali e partner esterni; Supportare la redazione e la sottomissione della documentazione richiesta per variazioni e procedure...

Cosmo sta cercando un/una Regulatory Affairs Specialist per la sede di Lainate. La risorsa farà parte del dipartimento Regulatory Affairs, collaborando con un team di specialisti e riferendo al Head of Global Regulatory Affairs. Responsabile di redigere, aggiornare e gestire documentazione regolatoria per medicinali in diverse aree geografiche, supportando...

Overview Within the Global Regulatory Affairs Operations department, whose mission is to provide timely and high-quality regulatory submission-ready packages to facilitate faster time to market, while driving business solutions that support the company’s cross-functional processes and advancing company’s digital capabilities, the resource, reporting to...

Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Tests, in order to expand the RA Team, is looking for a: Senior Regulatory Affairs Specialist FDA & International Registrations Key Responsibilities: * Define and implement regulatory strategies to...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

OverviewQuality Assurance Regulatory Affairs (QARA) Specialist – Dedalus. Remote in Italy. Part of the Global Quality and Assurance Team to drive quality and regulatory excellence in healthcare technology.What you’ll achieveAs a QARA Specialist you will ensure compliance with Quality and Regulatory standards across the company, contributing to better...

Select how often (in days) to receive an alert: Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. Over three years ago, we embarked on a transformative journey...

Cosmo è un’azienda innovativa focalizzata in tecnologie mediche (MedTech) attiva nello sviluppo di soluzioni basate su intelligenza artificiale, dermatologia, malattie gastrointestinali e CDMO. Collaboriamo con partner globali per migliorare la qualità delle cure e la vita dei pazienti. La nostra missione: costruire fiducia nella salute attraverso...

A multinational pharmaceutical company is seeking a CMC Senior Specialist in Bresso, Italy. The role involves managing regulatory submissions and ensuring compliance with cGMP and FDA standards. Candidates should have a degree in Life Sciences and over 5 years of Regulatory Affairs experience. Excellent English communication skills are essential. This...