Descripción de la oferta
LNP Manufacturing Manager¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.Our client, an American CDMO, is setting up their first site in Europe. It is a new state-of-the-art, full ATMP CDMO, located in Bilbao, Spain. We are looking for an experienced LNP Manufacturing Manager, able to produce the drug products for the mRNA already produced on the site. Key duties /Responsibilities:Manage the GMP, LNP manufacturing facility, to meet established delivery schedules and the company's stringent quality standards.QC expertise highly appreciated.Team leadership with hands-on experimental work, requiring a candidate who is comfortable with both guiding projects strategically and participating directly in experimental tasks.Support a culture of operational excellence where teamwork and active problem- solving lead to continuous improvement throughout the organization.Ensure that team activities, equipment, facilities, and personnel are operated and maintained in a state of compliance with appropriate requirements.Defend his/her area of responsibility in regulatory or customer audits.Minimum Qualifications:Degree in biopharma or related field.Must have a minimum of 10 years of experience in pharmaceutical/biotech industry with increasing responsibilities, including 4+ years in LNP manufacturing.Experience in overseeing GMP manufacturing activities at CDMOs or biopharma companies.Strong management and interpersonal/communication skills. Prior success in working effectively with senior scientific, medical and operations staff.Fluency in English. Spanish is also preferred.We offer:Join a new CDMO with unique, disruptive technology in a high-growth market.Help build a high-performance organization. xcskxlj Initiate and optimize GMP LNP manufacturing activities.
