Job Details

ID #53069284
State Kentucky
City Louisville
Job type Full-time
Salary USD TBD TBD
Source Eurofins
Showed 2024-12-13
Date 2024-12-13
Deadline 2025-02-11
Category Et cetera
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Process Development Scientist - Oligonucleotide Chemistry

Kentucky, Louisville, 40201 Louisville USA
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This is an exciting time to join the Eurofins Genomics LLC process development group. The company is rapidly expanding oligonucleotide manufacturing to support the increasing demand of molecular diagnostics. Process Development Scientist will work directly with some of the biggest companies in life sciences to manufacture and develop oligonucleotides (oligos) and support ever evolving needs. Eurofins Genomics LLC is a leading manufacturer of Oligonucleotide primers/probes/assays in addition to being a key supplier of oligos for other diagnostic applications.The Process Development Scientist will be an owner in area of expertise (oligonucleotide synthesis, purification, organic chemistry, and quality control). This position reports directly to the Director of Oligonucleotide ChemistryHands-on expertise in preparing chromatography and analytical techniques throughout the product development lifecycle, from early research to on-market support diagnosticsDemonstrated experience purifying, analyzing, and characterizing complex oligonucleotides and related analytical methods.Ability to develop innovative analytical methods for reagents and assay performance, applicable in R&D and Operations; supporting scale-up and launch effortsAbility to design and execute advanced troubleshooting experiments in coordination with collaborators; demonstrated experience developing creative assays to understand and detect system defectsAbility to support documentation transfer, specifically of prototype methods and documentation from research to development and manufacturingServe as a subject matter expert and provide expertise across R&D departments (oligo synthesis & purification, assay development) and operationsDocument all assays and results in a standardized, accurate, traceable, and timely mannerPerform mentor type duties including the training of more junior employeesAdhering to cGMP/cGLP documentation procedures according to FDA specificationsHPLC method development for specific DNA/RNA modifications, scales, lengths, and purityCustomization of method and mobile phases to maximize yields while maintaining qualityDevelop new downstream workflows for automated larger scale purification processDevelop and implement other purification processes (PAGE, Cartridge, etc) that expand portfolio for purification

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