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Role Overview:
- You will be responsible for carrying out all aspects of regulated studies from setup through reporting in a GLP-compliant environment.
- Leverage your bioanalytical expertise to ensure data integrity, troubleshoot issues, and deliver high-quality results.
- Act as a technical resource and study lead, providing work direction and training to junior scientific staff.
Qualifications:
- Bachelor’s, Master’s, or PhD in Chemistry, Biochemistry, or related field with at least 5 years of bioanalytical lab experience.
- Extensive hands-on experience with quantitative LC-MS/MS workflows and GLP-regulated environments.
- Proven ability to troubleshoot technical and operational issues in a production setting.
Benefits & Culture:
- You will enjoy company sponsored events, career growth through KCAS University, and an employee stock ownership program.
- Access to latest technology and paid time off to volunteer in the community.
- We are a purpose-driven team that values relational environment, constant development, and supportive leadership.
KCAS Bio
KCAS Bio is a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering drug development in both human and animal health fields. They foster a relational, purpose-driven culture with nimble, empowered teams committed to innovation and employee growth.