(Fixed-Term) Manufacturing Associate II - Shift Position

Adhering to Moderna’s safety procedures and maintaining housekeeping.,Executing operations activities according to cGMP, SOPs, and manufacturing documentation.,Collaborating with QA peers for timely closure of batch disposition documentation.,Participating in investigations (RCA) and CAPA tasks.,Utilizing performance tools to meet operational KPI objectives.,Responding to and troubleshooting routine equipment, process, and digital issues.,Proactively identifying and reporting compliance or health and safety issues.,Keeping training records and documentation up to date.,Performing routine maintenance tasks (e.g., lubrication, mechanical checks, filter changes) using hand tools.,Flexibility to work off-hours and overtime when necessary.,Contributing to multiple projects and continuous improvement initiatives.,Collaborating effectively in a dynamic, cross-functional matrix environment.

3+ years of experience in a GMP manufacturing environment.,A university degree with a specialization in Pharmaceutical production technology or equivalent.,Experience with filtration and chromatography, and cold chain management (a plus).,Experience in audit/inspection preparation, understanding Health authority and regulatory guidelines.,Ability to collaborate fluidly with peers, leadership, and cross-functional support groups.,Excellent written, oral communication, and organizational skills.,Ability to maintain attention to detail while executing multiple tasks with minimal supervision.,Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless.

University Degree (specialization in Pharmaceutical production technology or equivalent)

Must be willing to work off-hours and overtime when necessary, Position is site-based, requiring full-time presence at Moderna's site.