Development and Verification Scientist III
Alveo Technologies
Date: 7 hours ago
City: Alameda, CA
Contract type: Full time

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. Alveo’s 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: https://www.alveotechnologies.com/
Alveo Technologies is looking for a Development and Verification Scientist III to support ongoing Validation and Verification efforts for projects in disease detection. The Scientist will assist in planning and executing protocols and conducting wet experiments at the bench to meet objectives. This position will review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments.
You Will:
Assist with the Assay development of strategic initiatives and new products in the Assay Development R&D group.
Design and 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 department management and relevant stakeholders.
Assist cross-functional teams (Manufacturing formulations, Software development, Engineering) if needed.
Your Background Should Include:
A BA/BS or higher degree in Biochemistry, Molecular Biology, Microbiology or related field with 3-5 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 other technologies for gene target amplification using PCR and isothermal amplification methods.
Ability to work successfully across disciplines (including software, manufacturing, product development, quality, regulatory) 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 is highly desirable.
Experience in design control and product lifecycle management is highly desirable.
Ability to communicate effectively with scientists and engineers from a wide range of technical backgrounds and strong attention to detail is required.
Be self-motivated, able to manage multiple tasks, prioritizing effectively, etc.
Feel comfortable and thrive in a fast-paced cross-functional environment.
Excellent written and verbal communication skills.
This is an exempt position. Salary range is $97,000 - 103, 000.
We are an equal opportunity employer and value diversity at Alveo Technologies. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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. Alveo’s 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: https://www.alveotechnologies.com/
Alveo Technologies is looking for a Development and Verification Scientist III to support ongoing Validation and Verification efforts for projects in disease detection. The Scientist will assist in planning and executing protocols and conducting wet experiments at the bench to meet objectives. This position will review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments.
You Will:
Assist with the Assay development of strategic initiatives and new products in the Assay Development R&D group.
Design and 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 department management and relevant stakeholders.
Assist cross-functional teams (Manufacturing formulations, Software development, Engineering) if needed.
Your Background Should Include:
A BA/BS or higher degree in Biochemistry, Molecular Biology, Microbiology or related field with 3-5 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 other technologies for gene target amplification using PCR and isothermal amplification methods.
Ability to work successfully across disciplines (including software, manufacturing, product development, quality, regulatory) 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 is highly desirable.
Experience in design control and product lifecycle management is highly desirable.
Ability to communicate effectively with scientists and engineers from a wide range of technical backgrounds and strong attention to detail is required.
Be self-motivated, able to manage multiple tasks, prioritizing effectively, etc.
Feel comfortable and thrive in a fast-paced cross-functional environment.
Excellent written and verbal communication skills.
This is an exempt position. Salary range is $97,000 - 103, 000.
We are an equal opportunity employer and value diversity at Alveo Technologies. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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