Downstream Process Development Scientist

Framingham, MA

Currently I have an opening for a Downstream Process Development Scientist located in Framingham, MA. Details for the position are as follows:
 
Pay Range: $70-$90/hour

Job Description:
  • 12-month contract with the possibility of extending or converting to permanent based on performance and budget.
  • FULLY ONSITE
  • The Scientist, Downstream Process Development in MSAT will work in a matrix team management environment with global engineers and scientists to achieve robust and scalable purification processes to support 2nd generation processes, late-stage programs, and life-cycle management. This position will support the development of purification processes for a wide variety of molecules and modalities.
  • This role will play a key role in developing robust and scalable protein purification processes to deliver to the manufacturing group. As part of the MSAT group, this position will also support the manufacturing team to ensure the successful technology transfers to produce pharmaceutical drugs for life-saving therapies.
  • The drug substance function within global Manufacturing Science & Technology (MSAT) is the owner of Life Cycle Management (LCM) of DS Processes within the biologics manufacturing network. We deliver innovative, robust, and cost-effective next-generation processes and provide commercial manufacturing support. The function is responsible for tech transfer activities including process fit-gap assessment, process validation, preparing dossier sections, & PAI support to enable the launch of new and LCM products.
  • Work with a global group of engineers and scientists to develop robust and scalable downstream processes for monoclonal antibodies, bispecific antibodies, Fc-, Fab-, fusion proteins, enzymes, and other recombinant proteins to support GMP manufacture.
  • Work on MSAT development and pilot-scale projects, including regular team meetings and updates for, data management, investigations, technical report writing, and regulatory filings.
  • Ability to overcome challenges, with creative and innovative solutions.
  • Support the Develop and implement new cutting-edge technologies, for DSP sciences for life cycle management projects.
  • Support technology transfer including projects for internal and external partners.
  • Support DOE studies to establish proven and acceptable ranges (PAR) for process characterization.
BASIC REQUIREMENTS/QUALIFICATIONS:
  • M.S./M.A. in Biotechnology, or related field, with a minimum of 3+ years of relevant experience; OR
    B.S./B.A. in Biotechnology, or related field, with a minimum of 5+ years of relevant experience.
Preferred experience with
  • Commercial Downstream Manufacturing Support.
  • Downstream processes at the small to an intermediate scale of cGMP biologics production.
  • Chromatography, TFF including, UD/DF, micro filtration, nano filtration, and filtration
  • Process scaling and/or technology transfer.
  • Virus clearance studies
  • Automated chromatography platforms (e.g., Client Healthcare AKTA).
  • Authoring and executing protocols, interpretation of data, and report generation.
  • Operating and troubleshooting process equipment.
 

 

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