"Alerted.org

Lenexa, KS, USA

Full-time

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.

Job 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 Information

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.