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Lead complex bioanalytical studies, develop and validate methods, mentor junior staff, and ensure regulatory compliance while maintaining scientific quality.

As a Scientist II in BioPharma Sciences, you will conduct bioanalytical testing, manage projects from R&D to report preparation, and provide guidance to junior staff.

As a Scientist I, you'll execute studies, support method development, process data, troubleshoot assays, and maintain compliance with protocols in bioanalytical testing for drug development.

As an Associate Scientist, you'll design and analyze molecular and cell biology experiments, manage lab procedures, and train junior staff in a GLP environment.

As a BioPharma Associate Scientist, you will design experiments, supervise lab studies, and analyze data to support drug development efforts.

As Lead ELN/LIMS Administrator, you will manage ELN and LIMS systems, ensuring compliance, data integrity, and workflow efficiency while collaborating with various teams to drive improvements and training.

The Director of Quality Assurance at KCAS Bio oversees QA departments, manages quality systems, leads regulatory audits, and interacts with executive management and clients to ensure compliance and high-quality standards in bioanalytical services.

Serve as a technical lead for bioanalytical validations and biostudies, overseeing method development (LBA, LCMS, immunoassays), supervising staff, reviewing and reporting study results, mentoring scientists, troubleshooting assays, ensuring GLP/SOP compliance, and interfacing with sponsors and subcontractors to integrate and deliver high-quality study outcomes.

The Scientist II will execute studies in bioanalysis, focusing on LCMS techniques, data analysis, method development, and compliance with regulations.

The Associate Scientist will execute bioanalytical study activities, perform LC-MS analysis, support method development, and maintain documentation while communicating progress with senior staff.