Eurofins Lancaster Laboratories

Research Scientist/Senior Scientist - LC-MS/MS

Eurofins Lancaster Laboratories • $88K — $105K *
Lenexa, KS 66215In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
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Job Overview by Ladders

Qualifications

  • BS, MS, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemistry, or related field
  • 3-8+ years of bioanalytical laboratory experience
  • Hands-on experience with LC-MS/MS method development and validation
  • Knowledge of FDA, EMA, and ICH M10 method validation requirements
  • Experience with small molecules, peptides, oligonucleotides, ADCs, and mAbs
  • Strong technical writing and documentation skills
  • Excellent troubleshooting, organizational, and communication abilities

Responsibilities

  • Develop, optimize, qualify, and validate LC-MS/MS bioanalytical methods
  • Perform sample preparation, instrument operation, data analysis, and troubleshooting
  • Support routine sample analysis for preclinical and clinical studies
  • Assist with assay validation activities according to FDA, EMA, and ICH M10 guidance
  • Analyze data and contribute to study reports and technical documentation
  • Author and revise SOPs, work instructions, and validation protocols
  • Collaborate with cross-functional teams to ensure project success
  • Identify and implement opportunities for process improvements

Benefits

  • Comprehensive medical coverage
  • Dental and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
Full Job Description
Job Description

We are seeking a Research Scientist / Senior Scientist to support the growth of our bioanalytical LC-MS/MS capabilities within a regulated CRO environment. This role will contribute to method development, validation, transfer, and support sample analysis for a diverse range of therapeutic modalities, including small molecules, peptides, oligonucleotides, antibody-drug conjugates (ADCs), and monoclonal antibodies.

The successful candidate will bring hands-on experience in regulated bioanalysis and will work closely with scientific, operational, and quality teams to implement and execute assays in accordance with FDA, EMA, and ICH M10 guidance. In addition to laboratory-based activities, this individual will support SOP development, equipment onboarding, process improvement initiatives, and the integration of LC-MS/MS services into an established bioanalytical testing organization.

This is an excellent opportunity for a scientifically mature and collaborative professional who enjoys both technical problem-solving and helping build new capabilities in a growing laboratory environment.

Here's what you'll do:
  • Develop, optimize, qualify, and validate LC-MS/MS bioanalytical methods for regulated studies.
  • Perform sample preparation, instrument operation, data analysis, and troubleshooting.
  • Support routine sample analysis for preclinical and clinical studies.
  • Assist with assay validation activities in accordance with FDA, EMA, and ICH M10 guidance.
  • Analyze and interpret data and contribute to study reports and technical documentation.
  • Author and revise SOPs, work instructions, validation protocols, and technical reports.
  • Support onboarding, qualification, and maintenance of LC-MS/MS instrumentation and associated laboratory systems.
  • Collaborate with cross-functional teams including Quality Assurance, Operations, Project Management, and Scientific Leadership.
  • Identify and implement opportunities for process improvements and operational efficiencies.
  • Maintain compliance with applicable GLP, GCP, and company quality requirements.


Qualifications

The ideal candidate:

  • BS, MS, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemistry, or a related scientific discipline.
  • 3-8+ years of relevant bioanalytical laboratory experience.
  • Hands-on experience with LC-MS/MS method development and validation.
  • Working knowledge of FDA, EMA, and ICH M10 bioanalytical method validation requirements.
  • Experience with one or more of the following analyte classes:
    • Small molecules
    • Peptides
    • Oligonucleotides
    • Antibody-drug conjugates (ADCs)
    • Monoclonal antibodies (mAbs)
  • Experience supporting regulated bioanalytical studies and routine sample analysis.
  • Strong technical writing and documentation skills.
  • Excellent troubleshooting, organizational, and communication skills.
  • Experience in a CRO, pharmaceutical, or biotechnology environment.
  • Familiarity with hybrid LC-MS/LBA approaches.
  • Experience with Waters, Sciex, Thermo Fisher, or Shimadzu LC-MS/MS platforms.
  • Experience supporting SOP development and laboratory process implementation.
  • Experience with laboratory informatics systems, including LIMS and chromatography data systems.
  • Knowledge of assay validation, sample management, and regulated study workflows.


Additional Information

The position is full-time, Monday-Friday, 8 a.m.- 5 p.m., with overtime as needed. Candidates within a commutable distance of Lenexa, KS are encouraged to apply.
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

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About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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