Date: 11-May-2017
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Scientist, Staff (Oncology)
Be part of a team: initiating, developing, and validating IVD oncology kits for the liquid biopsy market
Plan feasibility testing, protocol development, optimization, verification, validation, and launch
Document research progress under a Quality Management System
Communicate progress directly with colleagues and senior management
Build and manage a small team of Research Associates
Design effective experiments and work with statistics and bioinformatics team
Perform basic data analysis (R, JMP, Excel)
Successfully interact with various functional roles (including Marketing, Software, Engineers, Quality, Manufacturing & Project managers) within the organization to drive project to completion.
Ph.D. in oncology, molecular biology or closely a related field and at least 4 years of industry experience
Excellent verbal and written communication skills, logical and analytical thinking, ability to multitask, work independently and on a team, and the ability to learn, troubleshoot, and problem solve
Understanding and familiarity with CLSI guidance
Product development for regulated markets (CE/IVD, FDA) is a huge plus
Experience with nucleic acid technology relating to PCR, qPCR, multiplex PCR, and digital PCR
Experience with next generation sequencing, target enrichment experience is a plus
Very strong analytical and problem solving skills
Adept with Excel, basic statistical analysis, programming (e.g. PERL, python) and databases experience (SQL) are a plus
Skilled at writing clear plans, reports and SOPs, experience with Design Control a plus
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Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/