Associate Engineer, Process Engineering

Philadelphia, PA, United States
Jul 20, 2021
Pharm Country
Required Education
Bachelors Degree
Position Type
Full time
Company Background:

Century Therapeutics is developing novel allogeneic living cell products for oncology that overcome the limitations of current cell therapies. Century's genetically-engineered, universal iPSC-derived immune effector cell products are designed to specifically target hematologic and solid tumor cancers. Our commitment to developing off-the-shelf cell therapies will expand patient access and provide an unparalleled opportunity to advance the course of cancer care.

Century's foundational technology is built on induced pluripotent stem cells (iPSCs) that have unlimited self-renewing capacity. This enables complex cellular engineering to produce controlled cell banks of modified cells that can be expanded and differentiated into desired immune effector cells, which can supply vast amounts of allogeneic, homogeneous therapeutic products. This platform differentiates Century from other approaches that utilize non-renewable donor-derived cells.


The Associate Engineer, Process Engineering will be responsible for developing manufacturing processes for Century's cellular therapy programs. This role will be responsible for process scale-up activities, characterization, and/or technical transfer activities of cell therapy programs. Candidates are expected to have experience designing, executing, and documenting scientific experiments. This role requires extensive collaboration with internal and external teams. The successful candidate will need strong scientific background, interpersonal skills, and ability to work collaboratively with other groups across organizations.

This role is based in Philadelphia (University City), PA.

  • Design, execute, and document process development experiments
  • Operate and maintain lab equipment
  • Author and review technical documents (batch records, SOPs, reports, etc)
  • Support tech transfer activities of processes to internal and external sites
  • Support preparation of CMC documents for regulatory filings
  • Foster a collaborative and scientifically rigorous team culture

  • Typically, a BS or MS degree in a relevant biological, technical, or engineering field and 4-6 years for BS, or 2-4 years for MS, of relevant professional experience.

  • Experience with cell culture and aseptic technique
  • Excellent oral and written communication skills
  • Knowledge of manufacturing and/or cGMP a plus

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