Descripción de la oferta
LNP Manufacturing ManagerOur client, an American CDMO, is setting up their first site in Europe. It is a new state-of-the-art, full ATMP CDMO, located inBilbao, 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.
