Bioinformatics Data Scientist / Engineer / QA
San Francisco, CA, United States
Position Role/Tile: Bioinformatics Data Scientist / Engineer / QA
Location: South San Francisco OR Pleasanton, CA .
How 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.
of assay, reagents, software, hardware designers and manufacturing will revolutionize healthcare through high throughput diagnostic systems.
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 tests
Work closely with scientists and engineers with data analysis & experimental design
Develop software and analysis pipelines for data mining large datasets and auto generation of reports
Develop classification algorithms and model data
Evaluate algorithms needed for filtering, clustering and qualification of data and Perform root cause analysis.
Collaborate and communicate with various teams and business units
How 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 experience
Data structures and common methods in data transformation
Pattern recognition and predictive modeling skills
Excellent programming skills in C++, Java and Python
Experience utilizing Matlab, JMP, R, PowerBI or SPSS
Experience working in regulated / validated environment is a major plus
Knowledge, Skills, Abilities
Understanding of clinical trial design and evaluation
Knowledge in Molecular Biology and Clinical Diagnostics
Strong understanding of qPCR and amplification curve data
Prior experience with US-FDA 510k product development/submission, 21 CFR Part 11, and ISO 13485 is highly preferred
Ability to present and communicate analytical and clinical study analysis results to non-experts
Ability to work independently and in a team environment
Central Business Solutions, Inc,
37600 Central Ct.
Suite #214
Newark, CA 94560.
Central Business Solutions, Inc(A Certified Minority Owned Organization)
Checkout our excellent assessment tool: http://www.skillexam.com/
Checkout our job board : http://www.job-360.net/
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Central Business Solutions, Inc
37600 Central Court Suite 214 Newark CA, 94560
Phone: (833)247-8800 Fax: (510)-740-3677
Web: http://www.cbsinfosys.com
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