Jobs at MSD Animal Health Technology Labs

Lead HCC (patient/consumer) experience strategy and governance at a pharmaceutical company. Drive cross-functional projects from research, journey mapping, and ideation through UX/UI prototyping, testing, data-driven optimization, and operational handover. Integrate digital, data, and AI capabilities, define KPIs, run A/B tests and analytics, standardize design methods, and embed capability and change across the organization.

Lead planning and medical oversight of clinical trials in cardiovascular and respiratory therapeutic areas. Manage study design, execution, monitoring, analysis, regulatory reporting, and publications. Collaborate cross-functionally and with external investigators, support business development, and maintain scientific expertise. Travel ~20% to manage clinical research projects.

Develop, test, and maintain software applications supporting scientific research. Collaborate with engineers, scientists, and product teams to deliver cloud- and AI-enabled solutions using modern web frameworks and data platforms. Participate in Agile teams, code reviews, troubleshooting, documentation, and adoption of emerging AI tools.

Develop and deploy BI analyses and visualizations to support Global Clinical Trial Operations; manage SDLC timelines and vendor relationships; lead requirements sessions, ensure data quality, build SQL queries and data models, test BI capabilities, train stakeholders, and translate complex data for non-technical users to inform clinical operations decisions.

Lead scientific and operational bioanalytical strategy across discovery portfolios for biologics, small molecules, conjugates and novel modalities. Oversee assay strategy, method development/validation, data quality, automation and harmonization; manage and develop bioanalytical and DMPK leaders; represent PDMB on cross-functional teams to enable candidate selection, translational interpretation, regulatory readiness, and portfolio decision-making.

Plan and manage real-world evidence and non-interventional outcomes research for hematology products. Design studies, author protocols and reports, manage vendors/budgets, develop payer dossiers, adapt local evidence, collaborate cross-functionally, present and publish results, and build scientific partnerships.

Lead and mentor a two-engineer team providing process automation support for a Hepatitis A vaccine manufacturing facility. Oversee automated control systems, ensure SDLC and GMP/GxP compliance, troubleshoot automation issues, drive process control improvements, support audits/inspections, and lead digital transformation initiatives to maintain inspection readiness and reliable product supply.

Support audit teams by building analytics, dashboards, and automations to provide real-time risk assessments and control insights using Power BI, UiPath, Dataiku, SQL/Python/R. Participate in financial, SOX, IT and process audits, document technical solutions, collaborate across finance analytics teams, and apply Agile methods.

Lead cybersecurity and IT risk management for Enterprise IT supporting global shared services. Advise executive leadership, embed risk governance into programs (e.g., SAP S/4HANA), drive compliance, improve cyber resilience, mentor teams, and translate technical risk into business impact.

Design, develop, and deliver global, modular analysis, reporting, and submission standards and tools for drug and vaccine projects. Develop and validate ADaM, efficacy, and safety programming standards; design complex algorithms; provide technical consultation to statisticians and programmers; drive data structures and contribute to departmental strategy ensuring CDISC SDTM/ADaM compliance and production-quality practices.

Lead multi-modal biomarker discovery in oncology by analyzing large clinico-genomic datasets (RNA-seq, WES/WGS, proteomics, imaging, single-cell, epigenetics). Apply deep learning, statistical learning, and predictive modeling, collaborate with AIML teams, and present findings to cross-functional stakeholders to inform translational and clinical development decisions.

Field-based veterinarian role partnering with Danish pig veterinarians and producers to provide on-farm problem solving, diagnostic support, account planning, education on vaccination, and drive commercial, sustainable swine solutions across Denmark.

Manage and monitor assigned clinical trial sites to ensure ICH-GCP, local regulation, and sponsor SOP compliance. Lead site start-up, initiation, routine monitoring, validation and close-out visits; prepare visit reports; maintain regulatory documentation in CTMS and eTMF; identify and resolve site performance and compliance issues; support audits/inspections; mentor junior CRAs; collaborate cross-functionally and develop new research sites to expand local clinical trial capacity.

Sell oncology therapies across a defined Ontario territory by building relationships with healthcare stakeholders, supporting therapy adoption, collaborating with cross-functional teams, planning territory strategies, and continuously developing oncology and healthcare system knowledge.

Lead inhalation drug-device combination product programs end-to-end, setting device development strategy, coordinating cross-functional teams, managing CDMOs and suppliers, ensuring design controls, verification/validation, aerosol performance, manufacturability, human factors, regulatory submissions, and commercial launch readiness.

Lead corporate strategic planning and PMO governance for enterprise priorities: translate strategy into OKRs, run quarterly QBR governance, manage end-to-end strategic initiatives, institutionalize agile delivery, drive risk/issue management, and provide executive-ready insights to enable timely decisions across cross-functional stakeholders.

Support QC laboratory maintenance and calibration programs: plan/schedule preventive maintenance, manage equipment histories, coordinate vendors, ensure GMP and FDA compliance, lead root cause analysis and process improvements, and maintain CMMS/SAP work order and calibration data.

Design, develop, and maintain scalable automated test suites using Robot Framework and Python; integrate tests into CI/CD pipelines; perform API/backend/integration testing; apply Gen AI to accelerate test design, data creation, script development, and defect analysis; collaborate with cross-functional teams to ensure quality, compliance, and continuous improvement across the testing lifecycle.

Lead coordination between company and 3PL to ensure SAP/COMET alignment, manage imports/exports, customs and freight forwarders, monitor KPIs (OTIF), maintain inventory reconciliations, support audits (Health Canada, Finance/SOX), manage EDI interfaces (TIBCO/Liaison/IDOC), and drive process improvements and regulatory compliance for pharmaceutical logistics.

Lead technical direction and architecture for global web platforms, driving standards, secure scalable architectures, CMS integrations, AI/GenAI adoption, CI/CD/DevOps practices, automated testing, and agile delivery across cross-functional teams.