About this opportunity
Stanford University lists this Senior Bioprocess Development Scientist - Protein Production opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
BUSINESS TITLE
Senior Bioprocess Development Scientist - Protein Production
WORK SCHEDULE:
Onsite
BUDGETED SALARY:
$120,000 - $140,000
NOTES:
This is initially an 18-month fixed term role with the possibility of extension based on performance and budgetary considerations.
Visa sponsorship is not available for this position. All candidates must be eligible to work and live in the U.S.
SCHOOL/UNIT DESCRIPTION:
Sarafan ChEM-H is an interdisciplinary institute focused on connecting Chemistry, Engineering, and Medicine for Human Health. The institute was founded as a joint venture of the Schools of Medicine, Engineering, and Humanities and Sciences. The proximity of world-class biologists, chemists, engineers, and clinicians at Stanford presents a unique opportunity to study human biology at a molecular level, to translate this knowledge into groundbreaking products and services that promote healthy living, and to educate a new cadre of “physician-scientist-engineers” who will lead a rapidly evolving industry. The institute’s Nucleus serves as shared laboratories where trainees from diverse disciplines in science, engineering and medicine pursue projects under the mentorship of the center’s Directors, thereby gaining hands-on skills in high-throughput screening, medicinal chemistry, metabolomics, protein chemistry, and structural biology.
POSITION SUMMARY:
The Microbiome Therapies Initiative (MITI) at Sarafan ChEM-H is seeking a highly motivated protein scientist for a role in our ambitious new effort to develop and produce commensal vaccines in-house at Stanford for clinical use. At MITI, we aim to take advantage of the tremendous promise of the microbiome to treat human disease. In this position, you will be MITI’s primary expert on protein expression and purification, reporting to the Associate Director/GMP Supervisor. You will lead the development, execution, and troubleshooting of an array of protein production strategies needed to support the success of the commensal vaccine platform. You will adapt these strategies for the GMP production of MITI’s clinical products, participating in the redesign of our GMP suite for vaccine production and in the in-house manufacturing, formulation, and release process itself. Your colleagues will be MITI’s GMP manufacturing, quality, and regulatory team members. You will collaborate with members of the Fischbach lab at Stanford who have created this novel vaccination strategy. Ideal candidates are self-starters, comfortable with autonomy, yet embrace opportunities to tackle new problems and challenges as part of a dynamic team in a start-up-like environment within the University. Key responsibilities will include:
Design, coordinate, execute, and troubleshoot protein expression and production processes across multiple projects
Work with the Associate Director to scale/adapt existing production processes for in-house GMP production
Perform GMP pilot and production runs as part of MITI’s manufacturing team
Author relevant SOPs, work instructions, and batch records, and participate in GMP trainings, document control, and CAPA processes
Contribute to CMC sections of Investigational New Drug (IND) applications
PREFERRED/DESIRED QUALIFICATIONS:
PhD in Biochemistry, Cell Biology, Molecular Biology, or a related field with 2+ years of relevant industry experience
Expertise in recombinant protein expression using bacterial and mammalian expression systems
Experience troubleshooting yield and stability problems using construct design and expression protocol adjustment
Expertise in recombinant protein purification, process workflow design, and downstream equipment operation
Proficient in comprehensive protein characterization, including purity and identity (SDS-PAGE), biophysical stability, and contaminant analysis (endotoxin)
Experience with in-process testing methods such as flow cytometry and ELISA
Experience working in a cGMP environment
Excellent communication and organizational skills
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.