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Method Development Scientist I

Labcorp
4+ years
$70,000 – $85,000
Madison, United States
1 June 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Method Development Scientist I

Location: Madison, Wisconsin, USA
Department: Bioanalytical Method Development
Job Type: Full-Time
Work Schedule: Monday – Friday (Day Shift)
Application Window: May 29 – June 8, 2026
Salary Range: $70,000 – $85,000 per year


Job Summary

The Method Development Scientist I is responsible for developing, transferring, troubleshooting, validating, and documenting LC-MS/MS bioanalytical methods used for the quantification of pharmaceutical compounds in biological matrices. The role combines scientific expertise, regulatory compliance, laboratory execution, and cross-functional collaboration to generate high-quality analytical data in a regulated laboratory environment.


Key Responsibilities

Method Development & Validation

  • Develop routine and complex LC-MS/MS bioanalytical methods for pharmaceutical compounds.

  • Support method development, optimization, and method transfer activities.

  • Design and execute laboratory experiments for analytical method development.

  • Assist with method validation and sample analysis activities.

  • Evaluate method performance and implement improvements where necessary.

Troubleshooting & Technical Support

  • Troubleshoot analytical challenges encountered during:

    • Method development

    • Method validation

    • Sample analysis

    • Method transfer activities

  • Identify root causes of technical issues and implement corrective actions.

  • Serve as a technical resource for laboratory staff and project teams.

  • Assist in training team members on analytical techniques and procedures.

Laboratory Operations

  • Perform laboratory activities within a regulated bioanalytical environment.

  • Operate and maintain LC-MS/MS instrumentation.

  • Ensure laboratory work is completed according to established timelines and quality standards.

  • Generate reliable, reproducible, and scientifically sound analytical data.

Documentation & Compliance

  • Maintain complete, accurate, and timely documentation.

  • Ensure compliance with:

    • SOPs (Standard Operating Procedures)

    • GLP (Good Laboratory Practices)

    • Regulatory requirements

    • Internal quality standards

  • Prepare technical reports, study documentation, and method-related records.

Data Analysis & Communication

  • Analyze analytical data and communicate findings effectively.

  • Support data-driven decision-making through technical recommendations.

  • Communicate method performance, project risks, and resource requirements.

  • Participate in internal technical discussions and client interactions.

Collaboration & Continuous Improvement

  • Collaborate with cross-functional teams to support project objectives.

  • Participate in client meetings and scientific discussions.

  • Contribute to departmental process improvements and operational efficiency initiatives.

  • Promote teamwork and a collaborative laboratory environment.


Minimum Qualifications

  • Bachelor’s Degree in:

    • Chemistry

    • Biochemistry

    • Analytical Chemistry

    • Related Scientific Discipline

  • 4+ years of analytical laboratory experience.

  • 4+ years of LC-MS/MS experience.


Preferred Qualifications

  • PhD in Chemistry, Biochemistry, Analytical Chemistry, or related discipline.

  • Bioanalytical laboratory experience.

  • Experience in:

    • Method development

    • Method validation

    • Method transfer

  • Knowledge of:

    • GLP

    • GMP

    • GCP

    • SOP-driven laboratory environments