Clinical Analytical Development Associate Scientist (6-Month Contract)

About the role

We are seeking a skilled and motivated Clinical and Analytical Development Associate to play a pivotal role in developing and verifying cell-based assays for a new clinical diagnostic analyzer. This position offers an exciting opportunity to contribute to groundbreaking advancements in biotechnology while working in a collaborative and fast-paced environment.

Vital is revolutionizing point-of-care diagnostics with our VitalOne platform, delivering real-time care wherever patients are. Our mission is to democratize health technology, making healthcare more accessible and proactive. Our global team of experts spans chemistry, software, engineering, and microfluidics. We thrive on change, operate on trust, and value diverse perspectives. Our growth-minded culture empowers front-line decision-making and fosters impactful work. We seek tenacious, bold individuals ready to transform healthcare. At Vital, your talent will make a difference as we work to ensure everyone has access to care when and where they need it.

Responsibilities

• Assay Development: Support optimization and verification efforts for a complete blood count panel with 5-part differential on an automated analytical platform.
• Integration: Troubleshoot reagents, consumables and complex instrumentation to ensure robust performance and reliability.
• Documentation: Maintain detailed records of experimental protocols, results, and conclusions in compliance with regulatory standards (e.g., FDA, CLIA).
• Collaboration: Work closely with interdisciplinary teams including scientists, engineers, and software to integrate assays into comprehensive diagnostic workflows.
• Troubleshooting: Identify and resolve technical challenges related to assay performance and integration, ensuring continuous improvement.
• Quality Control: Implement and maintain rigorous quality control measures to uphold assay consistency and reliability.
• Innovation: Stay updated with emerging technologies and contribute innovative ideas to enhance assay development processes and integration strategies.

Qualifications

• Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Biotechnology, Bioengineering or a related field.
• 2+ years of hands-on experience in clinical chemistry assay development, immunoassays, and/or cell-based assays within a biotech or diagnostic industry setting is preferred.
• Proficiency in molecular biology techniques such as PCR, qPCR, ELISA, flow cytometry, and other relevant assays.
• Prior experience in handling biological specimens is preferred.
• Experience with microfluidics, next generation sequencing instrumentation, and/or automated microscopy systems is highly desirable.
• Ability to follow good lab practices and pipetting techniques with a high level of manual dexterity.
• Ability to follow instructions, protocols and SOPs to conduct experiments using bioanalytical instrumentation.
• Ability to do scripting in python or other programming languages like R to automate workflows and processes.
• Familiarity with MS Word and MS Excel for data analysis and documentation.
• Strong analytical skills with the ability to troubleshoot technical issues independently.
• Excellent organizational skills, attention to detail and effective communication skills with the ability to collaborate in a team-oriented environment.
• Experience with regulatory requirements (e.g., FDA, CLIA) and quality management systems is advantageous.