.Sr. Engineer I, Drug Product, MS&T page is loaded Sr. Engineer I, Drug Product, MS&T Apply locations Madrid - Spain Drug Manufacturing time type Full time posted on Posted 2 Days Ago job requisition id R15861 The RoleJoining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.Moderna is solidifying its footprint within our international centre for analytical excellence in Madrid, a city known for its rich scientific heritage. This facility, the largest such center outside the United States, exemplifies our commitment to solidifying our manufacturing network and advancing our promising mRNA product portfolio. We're looking for talents who can contribute to our innovative research and development efforts.This Sr. Engineer position is part of the Drug Product (DP) Moderna's Manufacturing Science and Technology (MST) team, tasked with technical support of GMP operations across international and US sites. Working under the guidance of the Director, you will play a crucial role in liaising with DP Contract Manufacturing Organizations (CMOs) and Moderna sites to drive forward the portfolio of projects and initiatives supporting commercial lifecycle management, technology transfer, and drug product technologies.Here's What You'll Bring to the Table:Your key responsibilities will be:Supporting continuous improvement initiatives and complex technical projects for DP and Aseptic manufacturing operations globally.Collaborating with Moderna's DP Operations to establish robust and compliant manufacturing performance at drug product CMOs.Partnering with Technical development to investigate and resolve complex manufacturing issues at CMOs.Your responsibilities will also include:Writing or revising the appropriate GMP documentations.Automating, visualizing, and analyzing QC data and metrics, identifying trends and patterns, analyzing causality, formulating improvement proposals, and converting the insights with business teams to actions and plans for measurable business improvements.Representing MST as a subject matter expert (SME) on DP manufacturing data analysis with Digital, Operations, and Technical Development teams.Contributing to our process data management and overall knowledge management strategy
