Scorpion Therapeutics
Scientist, Analytical Operations
Scorpion Therapeutics, Oceanside, California, United States, 92058
Role Summary
Research Scientist for the Pivotal and Commercial Biologics Characterization team within Biologics Pivotal and Commercial Analytical Development. Role requires broad experience in analytical development across all stages—from early development to commercial launch with regulatory filing experience with the FDA and EMA. Focus on biochemical characterization and development of novel analytical methods to support clinical and commercial programs.
Responsibilities
Define excipient and process reagent testing and control strategies across the late-phase biologics portfolio, with a focus on product stability.
Drive continuous improvement of excipient strategies.
Support the design, justification, and execution of end-to-end control strategy development through proactive definition of product quality targets.
Deliver high-quality work packages to support Pivotal IND and marketing applications.
Present findings to internal and external cross-functional teams.
Author analytical test methods, study protocols, and technical reports.
Independently plan and execute experiments to support development and investigations.
Collaborate across Pharmaceutical Development & Manufacturing and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Clinical Development, and Technical Development to ensure timely delivery and successful commercialization of the late-stage biologics portfolio.
Drive adoption of novel and state-of-the-art characterization technologies and approaches.
Qualifications
BS degree in Biochemistry or a related discipline with at least six (6) years of experience OR
MS degree in Biochemistry or a related discipline with at least four (4) years of experience
Strong knowledge of mass spectrometry, experimental design, and assay development
Excellent communication skills (verbal, technical writing, and interpersonal)
Strong organizational and planning skills
Ability to think critically and creatively, work independently, and resolve problems using appropriate resources
Skills
Mass spectrometry
Analytical method development
Regulatory filing experience (FDA/EMA)
Data analysis and visualization tools (Python, R, JMP, Spotfire)
Communication and collaboration across cross-functional teams
Education
Preferred: PhD in Biochemistry or a related discipline
Additional Requirements
Familiarity with technologies such as mass spectrometry, analytical ultracentrifugation (AUC), size exclusion chromatography (SEC), reversed phase chromatography, ion exchange chromatography (IEX), capillary gel electrophoresis (CGE), light scattering (DLS, MALS), and molecular analysis
Knowledge of FDA and ICH guidelines related to drug substances and drug products
Experience with mass spectrometry analysis software (Protein Metrics, Thermo BioPharma Finder, Skyline)
#J-18808-Ljbffr
Responsibilities
Define excipient and process reagent testing and control strategies across the late-phase biologics portfolio, with a focus on product stability.
Drive continuous improvement of excipient strategies.
Support the design, justification, and execution of end-to-end control strategy development through proactive definition of product quality targets.
Deliver high-quality work packages to support Pivotal IND and marketing applications.
Present findings to internal and external cross-functional teams.
Author analytical test methods, study protocols, and technical reports.
Independently plan and execute experiments to support development and investigations.
Collaborate across Pharmaceutical Development & Manufacturing and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Clinical Development, and Technical Development to ensure timely delivery and successful commercialization of the late-stage biologics portfolio.
Drive adoption of novel and state-of-the-art characterization technologies and approaches.
Qualifications
BS degree in Biochemistry or a related discipline with at least six (6) years of experience OR
MS degree in Biochemistry or a related discipline with at least four (4) years of experience
Strong knowledge of mass spectrometry, experimental design, and assay development
Excellent communication skills (verbal, technical writing, and interpersonal)
Strong organizational and planning skills
Ability to think critically and creatively, work independently, and resolve problems using appropriate resources
Skills
Mass spectrometry
Analytical method development
Regulatory filing experience (FDA/EMA)
Data analysis and visualization tools (Python, R, JMP, Spotfire)
Communication and collaboration across cross-functional teams
Education
Preferred: PhD in Biochemistry or a related discipline
Additional Requirements
Familiarity with technologies such as mass spectrometry, analytical ultracentrifugation (AUC), size exclusion chromatography (SEC), reversed phase chromatography, ion exchange chromatography (IEX), capillary gel electrophoresis (CGE), light scattering (DLS, MALS), and molecular analysis
Knowledge of FDA and ICH guidelines related to drug substances and drug products
Experience with mass spectrometry analysis software (Protein Metrics, Thermo BioPharma Finder, Skyline)
#J-18808-Ljbffr