USA - Delaware - Millsboro (Intervet), United States of America
Onsite
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.
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.
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.
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 submissions for veterinary products.
Ability to influence and lead cross-functional teams, drive strategic initiatives, and collaborate effectively in a matrixed environment.
Strong project management skills, with experience managing multiple projects simultaneously across various stages of development.
Excellent communication, organizational, and problem-solving abilities, with demonstrated success in technical leadership roles within the biotechnology or biopharmaceutical industry.
Required Skills:
Analytical Method Development, Analytical Problem Solving, Analytical Thinking, Biological Analysis, Communication, Continuous Improvement Tools, Counterfeit Detection, Cross-Functional Teamwork, Identifying Customer Needs, Innovation, Leadership, Management Process, Method Transfer, Method Validation, Microbiological Analysis, People Management, Quantitative Assay, Regulatory Compliance, Team Leadership, Technical Transfer, Veterinary MedicinePreferred Skills:
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The salary range for this role is
$129,000.00 - $203,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
DomesticVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
06/4/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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