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

The Principal Scientist leads bioanalytical studies, setting scientific direction, overseeing method validation, and mentoring staff while maintaining compliance and scientific integrity.

The Quality Support Analyst ensures quality compliance, manages documentation, supports training coordination, and enhances Quality Systems at KCAS Bio, contributing to regulatory standards and efficient record-keeping.

The Quality Specialist I performs QA activities, document reviews, audits, and assists with quality improvements to ensure compliance with regulatory standards.

As an Analyst I at KCAS Bio, you will assist senior scientists in the Pharma Mass Spec Bioanalysis lab, working with GLP and GCP methods to support drug discovery and clinical studies. Responsibilities include processing samples, preparing reports, and creating experiment plans.

As Director of Business Development, you will expand new business, maintain existing accounts, connect with clients, and achieve sales goals for 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.

Performing method development for LC-MS/MS, including sample preparation, troubleshooting, and data analysis. Collaborate with scientists for critical project experiments.