What are the responsibilities and job description for the Principal Technical Scientist BioAssay Development position at NWRPros?
Client is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases including principles of translational medicine.
The Opportunity
Client is seeking a talented and motivated Principal Scientist with a strong background in characterizing protein therapeutics using mass spectrometry-based tools to provide technical oversight and execution of protein characterization activities in large molecule CMC analytical development group.
Key Responsibilities
Lead internal large molecule CMC-focused mass spectrometry and extended characterization activities including primary sequence determination, PTM analysis, and higher order structure characterization for large molecule CMC portfolio.
Develop phase-appropriate product extended characterization strategies for large molecule CMC portfolio including elucidation of structure for early vs. late phase programs as well as characterization strategy for product variants and forced degraded samples.
Hands-on, technical execution of LC-MS based characterization activities to support comparability evaluations, inform CQA assessments, determine structure-function-activity relationships, and further product understanding.
Author and review technical development documents and relevant sections of health authority filings.
Maintain timely and accurate lab records consistent with good documentation practices.
Ensure rapid and timely analytical support for cell-line, bioprocess, and formulation development activities.
Support late phase analytical development and product characterization activities for one or more large molecule programs in CMC development.
Contribute to the development & implementation of overall analytical control strategy to enable commercialization of complex biotherapeutics.
Oversee product characterization strategy and execution including elucidation of structure as well as characterization of forced degraded panel and minor variants.
Perform critical quality attributes (CQAs) assessments to support phase-appropriate control system strategy.
Provide oversight of analytical method transfer, qualification, and validation activities at external / internal QC laboratories.
Requirements
Principal Scientist : PhD in Analytical Chemistry, Chemical Engineering, Biophysics or related scientific discipline plus a minimum of 8 years direct CMC-focused analytical development experience for protein therapeutics in the biotech / biopharma industry; or BS / MS with 12 years of relevant experience.
Senior Scientist : PhD in Analytical Chemistry, Chemical Engineering, Biophysics or related scientific discipline plus a minimum of 5 years of direct CMC-focused analytical development experience for protein therapeutics in the biotech / biopharma industry or BS / MS with 8 years of relevant experience.
In depth knowledge and extensive hands-on experience developing and applying mass spectrometry-based methods (Intact / reduced MS, subunit analysis, peptide mapping, N- / O-glycosylation profiling, disulfide linkage determination, LC-MS / MS analysis) for protein sequence confirmation, identification and characterization of product variants, and comparability in the context of protein therapeutics.
Well versed in characterizing protein therapeutic product variants and forced degradation samples.
Previous experience authoring relevant IND / BLA sections (e.g. Analytical comparability, Elucidation of Structure, Justification of Specifications, etc.)
Previous experience in developing a wide array of analytical protein characterization and biophysical methods (e.g. HPLC-based methods, cIEF, capillary electrophoresis, LC / MS – based multi-attribute methods (MAM), peptide mapping, spectrophotometry, light scattering, etc.)
Demonstrated track record of successfully transferring and qualifying analytical methods for protein therapeutic development programs, developing control strategies, and successful health authority submissions
Strong grasp of statistical approaches for design-of-experiments (DoE) analytical method development, robustness testing, and data analysis.
Excellent communication, collaboration, organizational, and scientific problem-solving skills.
Salary Range : $160,000.00 - $205,000.00. Client offers a competitive benefit package, which includes a 401k, healthcare coverage and other benefits.
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