Century Therapeutics, Inc
Sr. Engineering Associate/Associate Engineer, Drug Product Development
Century Therapeutics, Inc, Branchburg Township, New Jersey, United States
Sr. Engineering Associate/Associate Engineer, Drug Product Development
Century Therapeutics, Inc
Location: Branchburg, NJ
Responsibilities
Develop and implement manufacturing processes capable of supplying clinical trials with material complying to product quality targets, current Good Manufacturing Practices (cGMP), and regulatory requirements
Support the delivery of engineered immune cells to internal and external groups
Identify novel solutions to address key technical challenges required for manufacturing platform success, such as cryo‑preservation and cell culture media optimization
Contribute to experimental strategy toward at‑scale cell differentiation, expansion, formulation, and in‑process testing
Collaborate with internal partners (Process Development, Analytical Development) to integrate stem cell process technology and optimize Century’s next‑generation manufacturing process
Maintain laboratory procedures, systems and electronic notebooks to ensure documentation of experimental activities
Travel up to 10%
Requirements
Experience with mammalian cell culture and media optimization
Experience with Rotea, LOVO, Xuri, and other cell culture unit operations is preferred
Understanding of cell biology/physiology and/or engineering fundamentals; experience with induced pluripotent stem cells (iPSC) is desirable
Understanding of bioprocess characterization and validation concepts, cGMP, and GLP
Dynamic and culturally astute team‑player, scientifically rigorous with excellent communication skills
Qualifications
BS/MS degree in cell biology, biochemistry, biochemical engineering, or related field, ideally with 2–6 years of relevant industry experience
Functional experience in mammalian cell culture process development, including molecular biology, aseptic techniques, and cryo‑preservation
Job Type: Full‑time
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Location: Branchburg, NJ
Responsibilities
Develop and implement manufacturing processes capable of supplying clinical trials with material complying to product quality targets, current Good Manufacturing Practices (cGMP), and regulatory requirements
Support the delivery of engineered immune cells to internal and external groups
Identify novel solutions to address key technical challenges required for manufacturing platform success, such as cryo‑preservation and cell culture media optimization
Contribute to experimental strategy toward at‑scale cell differentiation, expansion, formulation, and in‑process testing
Collaborate with internal partners (Process Development, Analytical Development) to integrate stem cell process technology and optimize Century’s next‑generation manufacturing process
Maintain laboratory procedures, systems and electronic notebooks to ensure documentation of experimental activities
Travel up to 10%
Requirements
Experience with mammalian cell culture and media optimization
Experience with Rotea, LOVO, Xuri, and other cell culture unit operations is preferred
Understanding of cell biology/physiology and/or engineering fundamentals; experience with induced pluripotent stem cells (iPSC) is desirable
Understanding of bioprocess characterization and validation concepts, cGMP, and GLP
Dynamic and culturally astute team‑player, scientifically rigorous with excellent communication skills
Qualifications
BS/MS degree in cell biology, biochemistry, biochemical engineering, or related field, ideally with 2–6 years of relevant industry experience
Functional experience in mammalian cell culture process development, including molecular biology, aseptic techniques, and cryo‑preservation
Job Type: Full‑time
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