Regulatory Affairs Lead — Biocides

Pharma Point S.r.l. è alla ricerca di una figura di Regulatory Affairs Manager da inserire nel team italiano di Milano.Riporta al Global Regulatory Affairs Manager a Parigi e guiderà le attività regolatorie per garantire la conformità dei prodotti ai requisiti italiani ed europei. La risorsa gestirà documentazione regolatoria per registrazioni, rinnovi...

Pharma Point S.r.l. è alla ricerca di una figura di Regulatory Affairs Manager da inserire nel team italiano di Milano. Riporta al Global Regulatory Affairs Manager a Parigi e guiderà le attività regolatorie per garantire la conformità dei prodotti ai requisiti italiani ed europei. La risorsa gestirà documentazione regolatoria per registrazioni, rinnovi...

Regulatory Affairs Manager | Biocides & Pest Control | Milan Our Client is an international company headquartered in Milan, a leader in the development and commercialization of biocides, insecticides for both professional and consumer use, and pest control solutions, with a strong focus on naturally derived and sustainable formulations. To strengthen its...

Pharma Point Srl, realtà farmaceutica operante in Italia, cercaRegulatory Affairs Manager per gestire documentazione regolatoria, rinnovi e variazioni per i medicinali in Italia, collaborando con il team Global.La figura coordinerà RCP, fogli illustrativi ed etichette, assicurando la conformità normativa nazionale ed europea. L’offerta prevede smart...

Pharma Point Srl, realtà farmaceutica operante in Italia, cercaRegulatory Affairs Manager per gestire documentazione regolatoria, rinnovi e variazioni per i medicinali in Italia, collaborando con il team Global.La figura coordinerà RCP, fogli illustrativi ed etichette, assicurando la conformità normativa nazionale ed europea. L'offerta prevede smart...

Regulatory Pharma Net - RPN seeks a Regulatory Affairs Manager to lead regulatory strategy and submissions for global markets. You will oversee CTD documentation, coordinate cross-functional teams, and advise clients on regulatory requirements across EU and international frameworks. The role emphasizes collaboration with clinical development and CMC...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

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

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build a world 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...