We are looking for a purification development expert in the development of pharmaceutical and biotechnology processes to meet we acquire, assess, or rapidly and economically develop process technology or production capabilities needed. The expert would able to guide work for the development of purification processes used for the clinical and commercial manufacture of therapeutic proteins. This expert will plan, provide protocols and advices in support of the development of protein purification, including chromatography, filtration, membrane separations, centrifugation, and validation of viral and contaminant clearance. In addition, the expert experience in the scale-up and technology transfer of purification processes to the manufacturing organization and process validation. This expert will also be expected to direct the technical activities of junior scientists. A hands-on, laboratory-based effort will be desirable.+21 Other Responses
Drug Discovery Laboratory Automation
We are a rd department in a pharmaceutical company. We run different assays not for screening purposes (means that the scale is relative small, maybe from 6-20 plates). Some of them are cell based assays and a sterile environment is required. At this point, we are trying to identify the areas that can be automated and looking for an outside consultant to help. Please contact me at via zintro. We are located at san francisco.Geographic focus of northern california thanks.+27 Other Responses
Protein Analytics And Characterization
This is a 12 month contract opportunity in california: post-doctoral fellow/scientist ii analytical development - protein analytics and characterization
as a member of the analytical development team, this position will support early to late stage
development focused on protein analytics and characterization. The successful candidate may
develop, transfer, and validate protein analytical methods for drug substance and drug product
release, stability and characterization.
conduct bench activities for protein analytical characterization of new drug candidates.
Optimize, and qualify test methods for assigned projects.
May assist with review technical documents including analytical method development reports,
method validation protocols and reports, standard operating procedures in compliance with
Actively support testing of new drug candidates at various stages of development.
Participate in technical transfer of assays to qc and process development and contract
laboratories in a cgmp or glp environment, if appropriate.
phd in relevant field with minimum of 0 to 2 years’ related academic experience in analytical
development for the post doc i; the sr post doc will have 2 to 4 years’ of post-doctoral
Experience with analytical techniques including but not limited to hplc, ce, spectrophotometric
assays, sds-page, elisa and light scattering is desirable.
Knowledge of statistical data analysis preferred.
Some experience with analytical, technical writing, communication and data management skills
Knowledge and/or understanding of working in a glp/gmp highly desirable.
Contact us here on zintro for further details.+9 Other Responses