Garuda Therapeutics is seeking a motivated Manufacturing Associate/Sr. Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Garuda’s GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required.
ROLE AND RESPONSIBILITIES
• Perform, verify, and support GMP Cell Culture manufacturing activities in a cleanroom environment
• Complete applicable GMP Manufacturing Batch Records, Forms, and associated documentation
• Support GMP materials release and labeling
• Transfer materials into the GMP cleanroom suites following proper wipe down procedures.
• Follow Personnel, Material, and Waste flow procedures related to GMP manufacturing of Cell Therapy products
• Restock cleanroom manufacturing areas as needed.
• Perform environmental monitoring sampling when needed.
• Support deviation investigations and CAPA activities
• Other related duties as needed
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• Associates degree is required (in a science-related discipline preferred) BA/BS degree preferred
• Minimum of 1 year of professional experience working on a cell-based therapeutic product is required
• Strong interpersonal skills & attention to detail
• Strong commitment to teamwork, collaboration, and professionalism
• Proficiency in working with MS Office Suite
• Able to handle a dynamic workload, multi-task, and perform effectively under tight deadlines
• Must be able to lift 30 lbs.
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