Jobs at MSD Animal Health Technology Labs

Leads statistical programming for late-stage drug and vaccine clinical development, including analysis datasets, tables, listings, figures, regulatory submission deliverables, and post-marketing support. Coordinates global internal and outsourced programming teams, manages project plans and resources, ensures quality and process compliance, and serves as the programming point of contact throughout the product lifecycle. Requires advanced SAS expertise, clinical trial programming, CDISC/ADaM knowledge, and project leadership.

Owns and supports Emerson DeltaV DCS automation across a GMP-regulated biologics manufacturing facility. Responsibilities include DeltaV design, configuration, coding, troubleshooting, system lifecycle management, validation, change control, deviation investigations, regulatory compliance, technology transfers, new product introductions, and digital manufacturing improvements. The role collaborates with Engineering, Operations, Quality, Validation, MES, OEM automation, and global technology teams.

Leads Emerson DeltaV automation system ownership, sustaining support, root-cause investigations, engineering projects, tech transfer, NPI validation, change control, and audit readiness in a GMP-regulated biopharmaceutical facility. Supports process control systems across manufacturing and utilities, integrates DeltaV with Siemens automation and PAS-X MES, develops digital manufacturing tools, authors technical documentation, and mentors engineering colleagues.

Field-based HIV pharmaceutical sales representative responsible for managing a territory, engaging healthcare professionals and specialty pharmacy stakeholders, communicating product information, developing account strategies, and driving adoption of the Virology portfolio. The role requires customer relationship management, payer and account planning expertise, compliant execution, collaboration with cross-functional teams, and frequent travel throughout Maryland and Northern Virginia.

Provides quality assurance oversight for pharmaceutical packaging and manufacturing operations. Responsibilities include shop floor support, batch record review, material control, defect resolution, GMP compliance, investigations, root cause analysis, corrective actions, SOP review, compliance trending, and continuous improvement. Supports third-shift operations and collaborates with manufacturing, suppliers, and cross-functional teams to maintain regulatory compliance, product quality, workplace safety, and reliable supply.

Manage end-to-end delivery of technical deliverables for clinical trials including planning, design, build, testing, deployment, change control, risk management, and post-release maintenance. Coordinate cross-functional stakeholders and vendors, ensure GxP/CSV compliance, maintain audit-ready documentation, and support inspections and archival activities.

Provides independent quality oversight for GMP computerized systems supporting pharmaceutical manufacturing, laboratories, infrastructure, and quality operations. Reviews and approves validation and SDLC documentation, maintains validated system status, supports audits and inspections, drives remediation of compliance issues, monitors system health, promotes data integrity and regulatory compliance, and mentors junior team members.

Leads operational integration for the Portfolio Management and Operational Enablement team within Digital Human Health. Oversees cross-team alignment, operating cadence, delivery quality, capacity planning, executive readiness, bottleneck resolution, and adoption of improved workflows and AI-enabled capabilities. Partners with senior leadership across finance, strategy, architecture, and IT to improve operational rigor, decision-making, efficiency, and cross-functional execution in a regulated environment.

Conducts risk-based Good Clinical Practice audits across investigator sites, studies, suppliers, and third-party collaborations. Prepares audit reports, communicates findings, supports corrective and preventative actions, manages deviations, escalates significant quality issues, and provides quality oversight for assigned studies. Uses analytics dashboards and quality metrics to identify trends and prioritize audit activities. Also supports clinical quality capacity planning and audit assignments. Travel is required 50%–70%.

Leads end-to-end clinical data management for assigned trials and standards initiatives, including eCRF and data validation tool development, UAT, data review, reconciliation, query management, database lock preparation, and quality oversight. Provides cross-functional coordination, regulatory compliance, process improvement, mentoring, training, and standards governance support with minimal supervision.

Leads global private-market access strategy for pharmaceutical treatments, developing partnerships with pharmacies, clinics, payers, fintechs, distributors, and direct-to-patient platforms. Designs patient financing navigation solutions, evaluates self-pay and direct-to-patient channels outside the United States, and scales successful financing models across assets and geographies. Requires senior-level partnership development, market access, commercial strategy, executive influence, and cross-functional leadership across global healthcare ecosystems.

Supports end-to-end intercompany accounting across multiple legal entities, including transaction processing, balance reconciliation, variance resolution, close activities, settlements, eliminations, consolidation reporting, audit documentation, SOX compliance, and process improvement. The role also prepares financial reports, communicates with global finance stakeholders, and helps improve automation and internal controls.

Supports brand and customer strategy for an oncology portfolio focused on women’s cancers. Responsibilities include market and customer analysis, competitive intelligence, portfolio planning, marketing and omnichannel campaign execution, promotional material development, scientific events, performance monitoring, budget tracking, forecasting, and cross-functional collaboration with sales, medical affairs, and market access teams.

Leads end-to-end manufacturing execution at a large animal health site, overseeing four production teams and Operations Services with approximately 1,000 employees. Owns safety, quality, delivery, cost, GMP compliance, operational stability, risk management, production readiness, continuous improvement, financial performance, and project execution. Builds high-performing teams, drives Lean and transformational change, ensures inspection readiness, and represents Operations on the Site Leadership Team.

Lead technical design, architecture, validation, and mass-production readiness for an animal wearable (collar). Drive cross-functional collaboration across R&D, NPI, Operations, and manufacturing to ensure reliability, manufacturability, RF/embedded integration, and field performance. Own technical metrics, risk mitigation, and product outcomes from concept through production and ongoing support.

Leads discovery, requirements analysis, solution design, backlog refinement, delivery support, adoption, and continuous improvement for strategic digital products. Partners with business, product, engineering, architecture, UX, QA, and implementation teams to define capabilities, metrics, user stories, and success outcomes. Uses generative AI, copilots, and agentic workflows to improve analysis, documentation, decision-making, and delivery while promoting responsible AI practices.

Develop web applications focused on AI use cases within a cross-functional agile team. Responsibilities include architecture, prototyping, TypeScript or Python development, code reviews, performance and scalability improvements, testing, and collaboration with product owners and UX designers. The role also involves applying DevOps and secure software development practices, using cloud platforms and infrastructure-as-code, and delivering high-quality solutions in an international pharmaceutical environment.

Design, develop, maintain and remediate complex Workday integrations and custom Workday applications. Gather business requirements, build integrations using Workday tools and middleware, ensure SDLC/change management compliance, perform code migrations, troubleshoot and optimize integrations, document technical specs, and collaborate with stakeholders and vendors to deliver scalable HR IT solutions.

Serve as Scrum Master for 1-3 cross-functional data and analytics teams, facilitating agile ceremonies, removing blockers, grooming backlogs with Product Owners, tracking team metrics, coordinating stakeholders, promoting Agile best practices and scaling frameworks (e.g., SAFe), and supporting onboarding and continuous improvement.

Leads the warm-water aquatic animal health R&D site in Singapore, including personnel, facilities, product development projects, quality systems, regulatory compliance, budgeting, and operational performance. Oversees vaccine and therapy development, staff hiring and development, asset management, GLP/RQS quality, EHS and animal welfare standards. Acts as legal and government representative while collaborating with veterinary, regulatory, commercial, marketing, sales, and production teams to advance aquaculture products.