Jobs at MSD Animal Health Technology Labs

Shapes healthcare policy and external affairs in Bulgaria to improve patient access to innovative solutions, with a focus on HPV vaccination and future launches. Builds relationships with policymakers, government bodies, regulators, industry associations, and other stakeholders; develops engagement strategies; represents the organization publicly; and collaborates with regional and European teams on policy initiatives.

Provides analytical and downstream process sciences support for biologics drug substance manufacturing. Leads assay development, qualification, validation, technology transfer, experimental design, data analysis, investigations, and process improvement projects. Supports small-scale chromatography, UFDF, filtration, equipment setup, sampling, and model runs. Authors technical documentation, SOPs, protocols, and reports while training team members and contributing to root-cause analysis, CAPAs, Lean Six Sigma initiatives, regulatory activities, and cross-site knowledge exchange.

Lead AI product change enablement for the GPTeal product line (prioritizing Gemini Enterprise) by designing and executing adoption programs, change assessments, communications, training content, and community engagement. Coordinate with product teams, influencers, and stakeholders to drive usage, track KPIs, maintain SOPs and resource hubs, and support workshops. Act as a user-obsessed change catalyst to embed AI tools into daily workflows and support global rollouts.

Develops and configures Benchling applications for laboratory sample and reagent inventory processes. Builds Python SDK and REST API integrations with enterprise and laboratory systems, designs data models and workflows, implements testing and CI/CD, investigates technical issues, and applies data integrity and security practices. Collaborates with scientists, product teams, vendors, and distributed engineering groups while using approved AI tools to improve automation and development productivity.

Information Technology Interns will work on real-world projects across cloud, infrastructure, cybersecurity, software development, data and analytics, AI and machine learning, user experience, or automation. The internship includes immersive rotations, mentorship, professional development, and collaboration with global IT teams. Successful interns may transition into Merck’s full-time Emerging Talent Rotational program after graduation.

Lead regional deployment of global poultry marketing plans across APSA, coordinate product launches and campaigns, provide regional strategic input, support portfolio and life‑cycle management, train and engage commercial teams, manage events and budgets, foster stakeholder collaboration, and travel extensively to support country operations and business growth.

Designs and executes functional, regression, integration, and non-functional testing for ServiceNow applications. Develops automated scripts and test data in AutomatePro, manages defects, validates data, documents results, improves QA processes, and expands automation coverage. Collaborates with engineers, product managers, delivery leads, and business stakeholders in Agile/Scrum environments. Supports junior team members and stays current with ServiceNow updates and testing methodologies.

Lead IAM assurance efforts: onboard and support consumers of IAM services, advise stakeholders on IAM best practices, enable IGA and PAM adoption (Delinea, SailPoint), collaborate with engineering/ops, identify automation and process improvements, and provide subject-matter expertise for secure, compliant identity services.

Lead cluster strategy and pre-launch product planning for Hong Kong, Macau, and Taiwan. Drive annual strategic planning, project management, cross-functional launch readiness, pipeline prioritization, business cases, stakeholder alignment, and coach a junior analyst to ensure timely execution and maximize product launch success.

Support cluster strategy and new product planning by conducting market and competitive research, building models and forecasts, synthesizing insights, and managing cross-functional workplans to drive execution and inform senior stakeholders.

Leads country-level automation, analytics, and AI initiatives supporting clinical trial operations. Identifies opportunities, develops business cases, translates requirements into solutions, oversees development and validation, manages dashboards and KPIs, ensures ICH GCP and regulatory compliance, and leads deployment, change management, governance, and scaling across countries and regions.

Drive sales, margin, and portfolio penetration across assigned accounts and territories. Manage distributor relationships, develop account plans, track pipelines and forecasts, and conduct business reviews. Build relationships with veterinarians, production managers, procurement leaders, and industry associations. Deliver technical presentations, collaborate with Marketing and Regional Species Teams, gather market intelligence, maintain CRM records, and ensure compliant, ethical business practices.

Manage and monitor assigned clinical trial sites to ensure compliance with ICH/GCP, sponsor SOPs and local regulations; perform site visits, oversight, documentation in CTMS/eTMF, support site selection, escalate and resolve site performance issues, and contribute as SME for monitoring processes.

Provide scientific and technical leadership for biologics process development across upstream and/or downstream operations. Drive platform-based strategies, knowledge sharing, process optimization, scale-up/scale-down modeling, troubleshooting, data-driven decisions, regulatory-ready documentation, and cross-functional alignment to ensure robust, scalable processes for clinical and commercial manufacturing.

Provide enterprise scientific leadership for vaccine drug substance process development and manufacturing across modalities. Define scientific strategy and technology roadmaps; guide upstream, downstream, analytical and scale‑up efforts; enable regulatory submissions and commercialization; build external partnerships; represent the organization externally; and mentor and develop scientific teams to drive innovation and program progression from preclinical through commercial stages.

Provide technical support and lead automation projects for manufacturing and packaging systems. Troubleshoot and optimize PLCs, HMIs, robotics, machine vision, motion control and industrial networks. Author validation and compliance documentation (IQ/OQ, SOPs), support SDLC/CSV, lead root cause analysis and continuous improvement, and integrate serialization/track-and-trace and digital manufacturing solutions.

Lead and grow a multi-site cheminformatics and data science team to develop scalable computational workflows, ML and knowledge-graph enabled models, and cloud-based platforms that accelerate drug discovery decision-making while partnering with IT and cross-functional scientific teams to ensure adoption and impact.

Lead quantitative pharmacology and pharmacometrics for oncology programs, design and execute PK/PD and population models, simulate trial designs, author regulatory documents, represent team in regulatory meetings, and mentor junior scientists to inform drug development decisions.

Lead early clinical development and translational medicine strategy for novel therapeutics. Design and execute Phase I–II clinical and pharmacology studies, develop biomarker strategies and validate platforms, provide target validation and clinical expertise, collaborate cross-functionally across discovery, regulatory, and clinical operations, and support worldwide regulatory filings and development decisions.

Lead value and real-world evidence strategy for oncology assets, designing and overseeing observational studies, economic models, AMCP and global value dossiers. Collaborate cross-functionally with clinical development, medical affairs, market access and country affiliates to support reimbursement, HTA submissions, publications, and presentations.