$80K — $100K *
About the Position
As the Upstream Process Development Scientist III, you will be a member of a team with experienced scientists. This team is responsible for development, scale-up, and technology transfer of cell culture processes for the clinical manufacturing of ARC and GADLEN pharmaceuticals expressed in mammalian expression systems. Responsibilities will include leading process development activities from the lab, experimental design, generation of protocols and data analysis, authoring and reviewing technical reports, support technology transfer into the pilot plant, generate documents for internal and external manufacturing of clinical stage programs, and CMC sections of regulatory filings. Primary responsibilities will include clone screening in microscale bioreactors with primary focus on host cell protein manipulation, expression levels and product quality assessments, technology development towards building a platform upstream process not limited to development of cell culture media and feed development but also include implementation of scalable cell culture methodologies. Integrating strategies to reduce impurities including HCP into process development workflows will be critical for success. Routine interactions with the downstream process development, analytical, research, quality, and regulatory groups at Shattuck is a must.
The Upstream Process Development Scientist III will be actively involved in working with the Technology operations leadership to develop strategic planning for development of a platform process for the ARC and GADLEN programs.
We are looking for professionals with these required skills to achieve our goals:
If you have the following characteristics, it would be a plus:
Valid through: 10/27/2021
$140K — $160K *
5 days ago