Associate Director, Analytical Technical Solutions (Animal Health)

Job Description

US Analytical Technology Solutions (US-ATS) supports all Animal Health sites globally in analytical method development, improvement, validation, transfer as well as in all kinds of analytical investigations. This position will lead and oversee all aspects of analytical life cycle management activities for in-line licensed products and introduce new innovative analytical technologies.

The Analytical Technical Solutions (ATS) Site Lead provides strategic, scientific, and operational leadership for analytical development activities across US sites. The role ensures compliant, efficient, and innovative analytical support for biologics, vaccines, and biotherapeutics while enabling cross‑functional alignment, regulatory readiness, and business continuity.

This position is in Millsboro, Delaware-US site. The position may require up to 10-15% of domestic and international travel.

Primary Responsibilities:

• Serve as a primary ATS liaison for Millsboro Site (Site Lead), acting as the primary point of contact for Tier meetings and cross-functional site-level forums with BTS, Quality, and other operational stakeholders.

• Provide strategic leadership to an analytical matrix team across multiple US sites to oversee biologics assay development, validation, transfer, improvement, and implementation for viral and bacterial vaccines as well as other biotherapeutics. Aligns site-level goals with broader organizational strategies and global analytical capabilities.

• Lead the implementation, qualification, and life-cycle management of analytical methods supporting raw materials, drug substance, and drug product testing.

• Develop, communicate, and execute strategic plans aligned with portfolio and pipeline priorities to ensure timely, high-quality analytical data delivery.

• Collaborate closely with cross‑functional partners including QC, R&D, Regulatory Affairs, Quality Assurance, Manufacturing, and site functional leaders to drive integrated development and testing strategies.

• Ensure compliance with global regulatory expectations (EMA, VSM/VICH/USDA, USP, ICH, GLP, etc.) and contribute to regulatory submissions, inspections, and dossier authoring.

• Provide scientific and analytical oversight for cGMP documentation, including change controls, deviations, CAPAs, method qualification/validation protocols and reports, method transfer documentation, and specification justifications.

• Drive innovation by identifying, evaluating, and implementing new technologies and analytical methodologies, including ligand-binding assays, immune-, molecular-, and cell-based assays.

• Interpret complex scientific data, troubleshoot analytical issues, and develop scientifically sound solutions that meet program and regulatory requirements.

• Drive continuous improvement and operational excellence through standardization, data integrity initiatives, harmonized procedures, and best practices across sites.

• Lead proactive resources and capacity planning to ensure alignment with development strategy and program timelines aligned with business priorities.

• Support Primary and Working Reference standard and critical reagent management, including qualification, aliquoting and long-term management across all end users of the materials.

Education Requirements:

• PhD or DVM in pharmacology, toxicology, veterinary medicine with 7+ years of relevant industry experience;

• OR Master’s degree in pharmacology, toxicology, veterinary medicine with 9+ years of experience;

• OR Bachelor's degree in pharmacology, toxicology, veterinary medicine with 10+ years of experience.

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Required Experience and Skills:

• Extensive knowledge of US, European, and international veterinary drug development requirements for both companion and production animals.

• Proven leadership experience managing technical teams, laboratory operations, and external partnerships or CRO collaborations.

• Deep expertise in bioanalytical techniques including ELISA, ligand-binding assays, protein chemistry, molecular biology, immunoassays, and cell-based assay development for biologics and large molecules.

• Demonstrated experience with analytical method development, transfer, qualification, validation/co-validation, transfer and continuous method improvement.

• Strong understanding of global regulatory requirements and experience supporting or authoring analytical sections in regulatory submis