Sr Scientist - BioPharma Sciences

KCAS Bio

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's, or PhD in Biology, Biochemistry, Immunology, or related field
  • 5+ years in a bioanalytical laboratory
  • Extensive experience in a GLP-regulated environment
  • Hands-on expertise in ligand binding assays (LBA), including ELISA and MSD
  • Proficiency with assay development, qualification, and validation
  • Strong understanding of precision and performance characteristics of assays
  • Experience with troubleshooting and providing solutions for assay issues

Responsibilities

  • Design and execute all phases of assigned projects including assay development and validation
  • Lead scientific efforts and provide training for junior staff
  • Manage client communications regarding study progress
  • Collaborate with Quality Assurance to resolve audit issues
  • Ensure final authority for sample identification and discrepancies
  • Maintain timeline adherence and communicate status updates
  • Ensure compliance with study protocols, SOPs, and GLP regulations
  • Prepare data summaries and finalized reports for clients
  • Serve as a technical expert in assay performance and troubleshooting

Benefits

  • Opportunities for professional development and training
  • Engagement in pioneering research projects
  • Supportive team environment with emphasis on mentorship
  • Exposure to the latest biopharmaceutical technologies
  • Commitment to company mission, vision, and values
Full Job Description
When you work as a Sr. Scientist in the BioPharma Sciences group at KCAS, you get to further our mission by leveraging your knowledge in bioanalytical and scientific principles to be responsible for carrying out all aspects of a study, from study setup through reporting, as well as development. You will also utilize your strong base in scientific principles/theories to assess data integrity and troubleshoot when necessary.

Our BioPharma Sciences team uses ligand binding assay (LBA) platforms to conduct bioanalytical testing in support of drug discovery, preclinical, and clinical studies, including the quantification of proteins, biomarkers, and anti-drug antibodies in biological matrices using technologies such as ELISA, MSD, and other immunoassay-based methods.

In this role, we will rely on you to:

  • Design and execute all phases of assigned projects including assay development, qualification/validation, troubleshooting, data analysis, and report generation
  • Act as lead scientist, help to design experiments, provide work instructions and technical training to more junior scientific staff in daily activities
  • Be responsible for all client communication related to study conduct
  • Interact with QAU to resolve identified audit issues and be accountable for continuous quality management in assigned studies
  • Have final authority for sample identification, including clinical site discrepancies and/or client
  • Be responsible for timeline adherence and communication of status to management as required
  • Ensure compliance of study activities with pertinent portions of study protocol, SOPs and GLP regulatory requirements
  • Prepare data summaries and final reports for client delivery
  • Act as a technical expert for assay performance, troubleshooting, and problem solving
  • Perform all aspects of the job in a way that supports company brand and supports company mission, vision, and values


To qualify for this role, you will have:

  • Bachelor's, Master's, or PhD in Biology, Biochemistry, Immunology, or related field with at least 5 years of experience in a bioanalytical laboratory environment
  • Extensive hands-on experience working in a GLP-regulated laboratory environment (required)
  • Strong experience with ligand binding assays (LBA), including ELISA, MSD, or similar immunoassay platforms
  • Experience with assay development, qualification, and validation for biomarker, PK, and/or immunogenicity (ADA) assays
  • Strong understanding of assay performance characteristics (precision, accuracy, sensitivity, selectivity, robustness)
  • Experience troubleshooting complex assay performance issues and optimizing assay conditions
  • Experience interacting with Quality Assurance and supporting audits and inspections
  • Prior experience acting in a study lead or Principal Investigator-type role is preferred


(Please note this is a representative summary of responsibilities, not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.)

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