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The Principal Scientist will lead bioanalytical activities, including assay design, development, validation, and execution. Responsibilities include supervising staff, improving lab procedures, troubleshooting assays, monitoring project expenses, and acting as a scientific resource both internally and externally.

The Bioanalytical Scientist manages laboratory staff to perform and analyze assays supporting clinical research. The role involves designing experiments, improving productivity, maintaining safe lab practices, and collaborating with other teams. Responsibilities include troubleshooting, supporting new procedures, writing project reports, and representing the company in scientific discussions.

The Scientist (Flow Cytometry) will participate in flow cytometry projects including assay development, validation, and execution. Responsibilities include performing assays, troubleshooting scientific issues, designing and presenting experiments, improving laboratory procedures, and collaborating with technical teams. The role also includes assisting with contract writing and scientific publications, while maintaining safe lab practices.

As a Customer Success Manager, you will lead onboarding, drive customer retention, manage relationships, gather feedback, and identify growth opportunities for QuartzBio's SaaS products in the life sciences sector.

The Principal Quality Assurance Auditor oversees quality and compliance activities in clinical studies, provides guidance on compliance issues, coordinates audits and assessments, and monitors quality systems to improve compliance. They also support the Quality Management System and participate in client audits and regulatory inspections.

The Commercial Strategy & Optimization Lead is responsible for enhancing the effectiveness of the Commercial organization by developing and implementing strategies, improving sales processes, and collaborating with multiple stakeholders to drive commercial initiatives.

The Safety Specialist II at Precision for Medicine is responsible for managing the intake and reporting of Serious Adverse Event (SAE) reports, independently handling complex studies while providing guidance on pharmacovigilance best practices. Key functions include interfacing with sponsors, participating in safety database assessments, preparing safety reporting plans, and mentoring new staff.