About Alveo
Alveo Technologies is the first company to make molecular detection and diagnostics universally accessible on the farm in the field in the clinic or in the manufacturing plant helping prevent or significantly limit the destructive impact of viruses fungi bacteria and other pathogens by detecting earlier at the Point of Need. Alveos rugged and portable multiplex-capable diagnostic platform employs IntelliSense its patented method of direct electrical sensing of nucleic acid amplification to provide affordable rapid and accurate results. By enabling early pathogen detection Alveo helps manage global health food security and supply chain resiliency by providing actionable insights at lightspeed. Know Sooner Act Faster with Alveo. For more visit: Technologies is looking for an Assay Development and Verification Scientist II to support ongoing Validation and Verification efforts for projects in disease detection. The Scientist will assist in planning and executing protocols and conducting experiments at the bench to meet objectives. This position will review understand and follow the instructions protocols and SOPs.
You Will:
Assist senior staff with the execution of strategic initiatives for the Assay Development Operation group.
Conduct technical experiments to develop sample-to-answer molecular diagnostics assays under strict project timelines.
Maintain control and propagate an exceptional quality of the documentation and analysis of results that will be submitted to regulatory agencies.
Proactively identify and escalate product risks and issues to their manager and relevant stakeholders.
Your Background Should Include:
A BA/BS degree in Biochemistry Molecular Biology Microbiology or related field with 1-4 years of IVD experience.
Familiarity with nucleic acid sample preparation from different origins.
Previous experience in molecular biology including principles of nucleic acid chemistry and gene target amplification using PCR and/or isothermal amplification methods.
Ability to work successfully across disciplines in a collaborative and cross-functional team environment.
Proficiency in MS Excel and experience in data analysis.
Experience working in biosafety level 2 (BSL-2) environment and willingness to work with infectious or otherwise biohazardous materials.
Experience in developing and commercializing diagnostic products in a GLP/cGMP environment is a must.
Previous experience in working in the IVD industry and understanding of ISO standards and QSR regulations is desirable.
Ability to communicate effectively with scientists and engineers from a wide range of technical backgrounds and strong attention to detail are a must.
Self-motivated able to manage multiple tasks as assigned and able to prioritize effectively.
Feel comfortable and thrive in a fast-paced cross-functional environment.
Excellent written and verbal communication skills.
Salary range for this position is $73191/year - $85250/year
Scientist II
