Central Business Solutions Inc.
Bioinformatics Data Scientist / Engineer / QA
Central Business Solutions Inc., San Francisco, California, United States, 94199
Position Role/Tile: Bioinformatics Data Scientist / Engineer / QA
Location:
South San Francisco OR Pleasanton, CAHow will you make an impact?
You will be a part of the fast-growing field of Clinical Diagnostics developing algorithms for molecular diagnostics based on real-time PCR technologies. We have played a pivotal role in the COVID-19 pandemic with the Taq Path COVID-19 Combo Kit for testing SARS-CoV-2. We continue to innovate and provide new solutions for the pandemic and we need your talent to help save lives. This is a dynamic career opportunity to join as a Bioinformatics, Data Scientist Team member to support our qPCR Algorithm Development Group.What will you do?
Organize and data mine / annotate clinical data to assess the performance of clinical testsWork closely with scientists and engineers with data analysis & experimental designDevelop software and analysis pipelines for data mining large datasets and auto generation of reportsDevelop classification algorithms and model dataEvaluate algorithms needed for filtering, clustering and qualification of data and perform root cause analysisCollaborate and communicate with various teams and business unitsHow will you get here?
Education:
Bachelor's degree in Molecular Biology, Biology, Chemistry, Applied Mathematics, Physics, Electrical Engineering, Computational Biology, Biostatistics, Bioinformatics, Computer Science or related discipline; postgraduate degree (Master's, PhD) is highly preferred.3+ years of product development experience (biotechnology industry preferred)Strong hands-on data analysis, modeling, and classifiers experienceData structures and common methods in data transformationPattern recognition and predictive modeling skillsExcellent programming skills in C++, Java and PythonExperience utilizing Matlab, JMP, R, PowerBI or SPSSExperience working in regulated/validated environment is a major plusKnowledge, Skills, Abilities
Understanding of clinical trial design and evaluationKnowledge in Molecular Biology and Clinical DiagnosticsStrong understanding of qPCR and amplification curve dataPrior experience with US-FDA 510k product development/submission, 21 CFR Part 11, and ISO 13485 is highly preferredAbility to present and communicate analytical and clinical study analysis results to non-expertsAbility to work independently and in a team environment
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Location:
South San Francisco OR Pleasanton, CAHow will you make an impact?
You will be a part of the fast-growing field of Clinical Diagnostics developing algorithms for molecular diagnostics based on real-time PCR technologies. We have played a pivotal role in the COVID-19 pandemic with the Taq Path COVID-19 Combo Kit for testing SARS-CoV-2. We continue to innovate and provide new solutions for the pandemic and we need your talent to help save lives. This is a dynamic career opportunity to join as a Bioinformatics, Data Scientist Team member to support our qPCR Algorithm Development Group.What will you do?
Organize and data mine / annotate clinical data to assess the performance of clinical testsWork closely with scientists and engineers with data analysis & experimental designDevelop software and analysis pipelines for data mining large datasets and auto generation of reportsDevelop classification algorithms and model dataEvaluate algorithms needed for filtering, clustering and qualification of data and perform root cause analysisCollaborate and communicate with various teams and business unitsHow will you get here?
Education:
Bachelor's degree in Molecular Biology, Biology, Chemistry, Applied Mathematics, Physics, Electrical Engineering, Computational Biology, Biostatistics, Bioinformatics, Computer Science or related discipline; postgraduate degree (Master's, PhD) is highly preferred.3+ years of product development experience (biotechnology industry preferred)Strong hands-on data analysis, modeling, and classifiers experienceData structures and common methods in data transformationPattern recognition and predictive modeling skillsExcellent programming skills in C++, Java and PythonExperience utilizing Matlab, JMP, R, PowerBI or SPSSExperience working in regulated/validated environment is a major plusKnowledge, Skills, Abilities
Understanding of clinical trial design and evaluationKnowledge in Molecular Biology and Clinical DiagnosticsStrong understanding of qPCR and amplification curve dataPrior experience with US-FDA 510k product development/submission, 21 CFR Part 11, and ISO 13485 is highly preferredAbility to present and communicate analytical and clinical study analysis results to non-expertsAbility to work independently and in a team environment
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