Description

Position Overview

The Director of Bioanalytical Services – LCMS is an exciting opportunity to put your mark on the design and build out of a fully functioning lab and operation in support of LCMS and Chromatographic assay development, validation and sample analysis.  The role will provide scientific, strategic, and operational leadership across all LCMS-based bioanalytical services. This role requires deep expertise in method development and validation for both small molecules (e.g., NCEs, metabolites) and biologics (e.g., peptides, proteins, ADCs, oligonucleotides) in biological matrices. You’ll lead a team of experienced scientists and work closely with clients to ensure timely, compliant, and high-quality data delivery.

Qualifications

Key Responsibilities

• Design and build out of laboratory and capabilities for LC-MS/MS bioanalytical services.
• Lead LCMS bioanalytical operations for both small molecule and large molecule (biologic) programs.
• Direct method development, validation, and regulated sample analysis under GLP/GCP/CLIA.
• Build and mentor a high-performing team of scientists and technical staff.
• Oversee implementation of LCMS strategies for complex modalities such as peptides, ADCs, and oligonucleotides.
• Ensure regulatory compliance with FDA, EMA, and ICH guidance.
• Manage departmental resources, project timelines, and instrumentation (e.g., SCIEX, Thermo, Waters, Watson).
• Act as scientific liaison in client meetings, regulatory audits, and cross-functional collaborations.
• Support business development and marketing with technical input for proposals and feasibility assessments.

Qualifications

• Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related field; M.S. with extensive experience considered.
• 10+ years of progressive experience in a bioanalytical lab environment, with a strong focus on both small molecule and biologics LCMS and supporting automation.
• Demonstrated leadership in a CRO, pharmaceutical, or biotech setting.
• Hands-on expertise in quantitative LC-MS/MS for both small and large molecules.
• Deep understanding of regulatory expectations for bioanalytical method validation (GLP/GCP and ICH-M10 requirements).
• Excellent communication, project management, and client-facing skills.

Preferred Experience

• LCMS-based analysis of biotherapeutics including intact protein quantitation, peptide mapping, and oligonucleotide quantitation.
• Familiarity with hybrid LBA-LCMS workflows (e.g., immunocapture-LCMS).
• Experience in supporting PK/PD, toxicokinetic, and immunogenicity studies.

Why Join Us?

• Lead a strategic function at the forefront of modern bioanalysis.
• Work with diverse modalities and advanced LCMS technologies.
• Competitive compensation and full benefits package.
• Opportunity to shape and grow LCMS capabilities within a dynamic organization.

Additional Info

Additional information 

COMPREHENSIVE BENEFITS PACKAGE & COMPENSATION

• As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.  We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.
   

• Authorization to work in the United States without Sponsorship 

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Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Company Description

About Us

Eurofins Pharma Bioanalytics Services is a leading bioanalytical contract research organization (CRO) supporting preclinical and clinical drug development. We specialize in delivering high-quality, regulatory-compliant data through innovative bioanalytical services. As we expand our capabilities, we are seeking a seasoned Director of Bioanalytical Services – LC/MS-MS to oversee and drive our hybrid portfolio of small molecule and large molecule bioanalysis.