What are the responsibilities and job description for the Manufacturing Associate position at Garuda Therapeutics?
Garuda Therapeutics is seeking a motivated Manufacturing Associate or Senior 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 :
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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
- Associates degree is required (in a science-related discipline preferred) BA/BS degree preferred
- 0- 2 years of professional work experience in a cell based therapeutic product is preferred
- 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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