Descripción de la oferta
LNP Manufacturing Manager 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. Initiate and optimize GMP LNP manufacturing activities.
