System One
Downstream Manufacturing Scientist
System One, Piscataway, New Jersey, United States,
Job Title:
Downstream Manufacturing ScientistLocation:
Greater Piscataway, NJ areaHours:
1st shift 8am-5pmType:
Direct HireSalary:
85K
Responsibilities:As a Downstream Manufacturing Scientist, you would be responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian-based biosimilars.You will be responsible for the purification of 50L to 1000L volumes engineering, clinical, and commercial batches in a cGMP environment.You need to have technical expertise in AKTA purification skids or similar and Tangential Flow Filtration (TFF).You should be knowledgeable about initiating batch records, protocols, investigations, and other technical documents.Requirements:Bachelor's or Master’s degree in chemical, biological, or biochemical sciences.4-5 years of experience in the biopharmaceutical industry.Previous experience working in a GMP and an aseptic manufacturing environment.Experience working with AKTA Process skids or similar.Familiarity with single-use manufacturing consumables such as bags, tube sets, columns, and process manifolds.Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation.Basic computer skills, including knowledge of Word, Excel, and spreadsheets.Knowledge of GMP batch manufacturing and packaging documentation; audit and review.Knowledgeable in cleaning verification/validation.
#J-18808-Ljbffr
Downstream Manufacturing ScientistLocation:
Greater Piscataway, NJ areaHours:
1st shift 8am-5pmType:
Direct HireSalary:
85K
Responsibilities:As a Downstream Manufacturing Scientist, you would be responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian-based biosimilars.You will be responsible for the purification of 50L to 1000L volumes engineering, clinical, and commercial batches in a cGMP environment.You need to have technical expertise in AKTA purification skids or similar and Tangential Flow Filtration (TFF).You should be knowledgeable about initiating batch records, protocols, investigations, and other technical documents.Requirements:Bachelor's or Master’s degree in chemical, biological, or biochemical sciences.4-5 years of experience in the biopharmaceutical industry.Previous experience working in a GMP and an aseptic manufacturing environment.Experience working with AKTA Process skids or similar.Familiarity with single-use manufacturing consumables such as bags, tube sets, columns, and process manifolds.Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation.Basic computer skills, including knowledge of Word, Excel, and spreadsheets.Knowledge of GMP batch manufacturing and packaging documentation; audit and review.Knowledgeable in cleaning verification/validation.
#J-18808-Ljbffr