Sr Scientist - Mass Spec Bioanalysis Production (LC-MS/MS)
Quick Summary
Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what we get to do every day at KCAS Bio.
As a Senior Scientist at KCAS Bio, you will serve as a lead technical contributor on complex bioanalytical studies, with the ability to independently execute and/or oversee all phases from study setup through final reporting, including method development and validation.
Leveraging a strong foundation in scientific principles, you will evaluate data quality, troubleshoot complex technical challenges, and ensure compliance with applicable regulatory standards.
In this role, you will act as a trusted internal expert, contributing to the advancement of scientific quality and operational efficiency while mentoring and developing less experienced scientific staff.
- Serve as lead scientist on complex studies, independently designing, executing, and troubleshooting bioanalytical methods and workflows.
- Demonstrated experience as PI on complex or high-visibility programs, including multi-analyte, multi-matrix, or global studies
- Experience supporting regulatory submissions (IND, NDA, BLA) with bioanalytical data as acting PI or key contributor
- Develop, optimize, and validate analytical methods to support drug discovery and development programs.
- Provide advanced troubleshooting support for method performance, instrumentation, and study execution issues.
- Author and review validation protocols, study plans, reports, and investigations in accordance with regulatory and quality standards.
- Provide scientific and technical support for sponsor interactions, contributing data interpretation and study rationale as needed.
- Develop and maintain SOPs and provide guidance on analytical procedures.
- Stay current with evolving scientific methodologies, instrumentation, and industry trends; apply knowledge to improve study quality and operational efficiency.
- Mentor Scientists and junior staff through hands-on training, technical guidance, and knowledge sharing.
- Perform all duties in alignment with company mission, values, and quality expectations.
- Bachelor’s degree in a scientific discipline (advanced degree preferred).
- 10–12+ years of relevant experience in research, CRO, or pharmaceutical environment.
- Expert knowledge of applicable laboratory techniques and instrumentation.
- Strong understanding of regulatory requirements and quality systems.
- Strong attention to detail and commitment to scientific excellence.
- Effective written and verbal communication skills.
- Strong technical writing and basic computer proficiency.
- Willingness and ability to mentor and coach others.
- Ability to function as a senior individual contributor and scientific role model.
Location & Eligibility
Listing Details
- Posted
- November 1, 2022
- First seen
- April 3, 2026
- Last seen
- May 5, 2026
Posting Health
- Days active
- 32
- Repost count
- 0
- Trust Level
- 25%
- Scored at
- May 6, 2026
Signal breakdown
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