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. Youll 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
Eurofins is a M/F Disabled and Veteran Equal Employment Opportunity and Affirmative Action employer.
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Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time