System One
Upstream Manufacturing Scientist
System One, Piscataway, New Jersey, United States,
Job Title : Upstream Manufacturing ScientistLocation : Greater Piscataway, NJ areaShift : 1st shift 8am-5pmSalary : $85KType : Direct
Responsibilities:As an Upstream Manufacturing Scientist, you would be responsible for executing mammalian cell culture processes and producing recombinant proteins for a wide range of mammalian-based biosimilars.The upstream scientist is responsible for executing cell culture batches from 50 L to 1000 L volumes, engineering and clinical batches in a cGMP environment.Execute batches in a team environment and work independently with minimum supervision as appropriate to the task at hand.Requirements:Technical expertise in bioreactor operations and cell biology.Knowledge of initiating batch records, protocols, investigations, and other technical documents.Bachelor's or Master’s degree in chemical, biological, or biochemical sciences.Seeking 3+ years of related experience in the biopharmaceutical industry.Experience with independently conducting and directing the design, execution, analysis, and documentation of all stages of process development.Previous experience working in GMP and aseptic manufacturing environments.Experience working with single-use manufacturing consumables such as bags, tube sets, columns, and process manifolds.Strong fundamental knowledge and subject matter expertise to execute engineering and clinical batches.
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Responsibilities:As an Upstream Manufacturing Scientist, you would be responsible for executing mammalian cell culture processes and producing recombinant proteins for a wide range of mammalian-based biosimilars.The upstream scientist is responsible for executing cell culture batches from 50 L to 1000 L volumes, engineering and clinical batches in a cGMP environment.Execute batches in a team environment and work independently with minimum supervision as appropriate to the task at hand.Requirements:Technical expertise in bioreactor operations and cell biology.Knowledge of initiating batch records, protocols, investigations, and other technical documents.Bachelor's or Master’s degree in chemical, biological, or biochemical sciences.Seeking 3+ years of related experience in the biopharmaceutical industry.Experience with independently conducting and directing the design, execution, analysis, and documentation of all stages of process development.Previous experience working in GMP and aseptic manufacturing environments.Experience working with single-use manufacturing consumables such as bags, tube sets, columns, and process manifolds.Strong fundamental knowledge and subject matter expertise to execute engineering and clinical batches.
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