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.