Merck is seeking a Senior Specialist in Business Insights & Analytics for their US Oncology, Digital Human Health team. This role focuses on leveraging data to provide strategic insights for commercial teams, inform go-to-market strategies, and drive customer understanding. The individual will translate business needs into analytical plans, collaborate with cross-functional teams, and stay updated on industry trends, including the application of GenAI. Experience with healthcare data, particularly EMR/EHR and claims data, is required, along with a strong understanding of commercial analytics and technology. The role emphasizes an entrepreneurial and consultative approach, with a need to understand the responsible use of AI in a regulated environment.

Seeking a Senior Manager for Strategic Forecasting in the pharmaceutical industry. This role involves leveraging analytics and technology to forecast long-range pharmaceutical asset performance across product lifecycles. The ideal candidate will use advanced analytical techniques like Monte Carlo simulations, agent-based modeling, NLP, and clustering to drive decision-making and improve forecast accuracy. Responsibilities include conceptualizing and delivering forecasts, collaborating with stakeholders, driving innovation and automation, and managing a team.

Associate Director, Technical Product Management at Merck, focusing on integration platforms within the healthcare domain. The role involves collaborating with stakeholders, translating business requirements into technical specifications, and leading agile teams to implement solutions. It requires evaluating emerging technologies like AI/ML, managing product roadmaps, and ensuring scalability, security, and compliance with health sciences regulatory standards (HIPAA, FDA).

The Business Analyst – Automation, Analytics & AI supports the identification, delivery, and sustainment of country-level automation, analytics, and AI solutions that enhance clinical trial operations. This role involves business case preparation, data analysis, dashboard/report building, workflow documentation, solution testing, training, and user support, ensuring solutions are compliant, adopted, and continuously improved.

Manager for a strategic forecasting team in the pharmaceutical industry, focusing on applying advanced analytics and statistical techniques to forecast product potential and inform decision-making. The role involves collaborating with stakeholders, driving innovation, and ensuring forecast accuracy.

This role leads the AI and Technology strategy for Merck's Digital Human Health (DHH) commercial business in China. The Director will partner with commercial leaders to define and execute an AI strategy focused on high-impact use cases, translate business problems into technology solutions with clear business cases, and drive adoption. The role requires a blend of strategic thinking, business acumen, understanding of AI, and stakeholder management, with a focus on delivering measurable business value through AI and data capabilities.

This is a working student position in Digital Marketing at Merck in Munich. The role involves supporting the planning, implementation, and analysis of digital marketing campaigns, content creation for social media and e-learning platforms, website maintenance, market analysis, reporting, and assisting with new product introductions and tool integration. The ideal candidate is a student with a background in marketing or communications, a strong affinity for new technologies and AI, and good communication and organizational skills.

This role focuses on developing and delivering data and analytics for the Vaccines Global Commercial Pipeline Analytics team within Merck's Digital Human Health (DHH) division. The primary responsibilities include portfolio analytics, hands-on analytics project delivery using tools like Excel-VBA, SQL, R, Python, and PowerBI, and stakeholder collaboration to inform strategic decisions. The role requires experience in insights & analytics, advanced analytics, market research, or strategic planning within the pharmaceutical industry, with a strong emphasis on commercial Vaccines data and patient analytics.

This role is responsible for the registration of new animal health products (biologicals and pharmaceuticals) and managing variations with health authorities, specifically APQA in Korea. It also involves managing local Quality Control (QC) matters with a pharmacist, overseeing the DPOC role, preparing for pharmacy inspections, and handling pharmacovigilance and complaint reporting.

Chief of Staff and PMO Lead at a biopharmaceutical company focused on research and development. The role supports the Managing Director and leadership team in executing core strategy, coordinating priorities, overseeing projects, and facilitating new ways of working. Responsibilities include strategic planning, performance reporting, project management, and driving organizational change. Requires strong strategic thinking, analytical skills, business acumen, and influencing abilities, with a preference for management consulting or biopharmaceutical experience.

Executive Director leading a cross-functional team to manage the strategy, oversight, and delivery of end-to-end activities for new or marketed oncology drugs, from discovery through reimbursement.

Associate Director, Quality Systems role at Merck focused on the execution, oversight, and continuous improvement of globally governed quality system processes within the clinical supply chain for investigational medicinal products. The role emphasizes driving transformation initiatives in deviation management, CAPA, change control, quality risk management, and data governance, ensuring compliance with global regulatory requirements and internal standards. It involves partnering cross-functionally, developing quality system metrics, and maintaining expert knowledge of GxP requirements.

Senior Director of Medical Affairs for Breast Cancer at Merck, responsible for executing global medical and scientific affairs plans, acting as a subject matter expert, and collaborating with various internal and external stakeholders to drive strategic planning and execution in the US and globally.

This role is for a Medical Science Liaison (MSL) in Oncology, focusing on field-based scientific exchange with healthcare professionals. The MSL will provide and gather medical and scientific information, build relationships with key opinion leaders, and support internal medical strategy and data generation efforts. The role requires advanced scientific/clinical knowledge, experience in a medical affairs field role, and strong communication skills regarding clinical data. Compliance with pharmaceutical regulations is critical.

The Global Director Medical Affairs (GDMA) – Precision Medicine Excellence & Operations Lead at Merck is responsible for designing, operationalizing, and improving systems and standards for diagnostic readiness at scale. This role leads the Precision Medicine / Diagnostics Capabilities Program and the Center of Excellence & Innovation Hub, drives global pathology education and medical societies strategy, and ensures operational excellence in cross-asset congress operations and pan-tumor publications. The role requires experience in capability design, implementation, and program management within a global matrix environment, with a focus on precision medicine and diagnostics in the pharmaceutical/biotech industry.

The Production Planning Analyst is responsible for ensuring the efficiency and effectiveness of production processes, optimizing resource utilization to meet market demands. This role involves production planning, inventory control, data analysis, interdepartmental collaboration, and participation in S&OP processes, with a focus on production control principles like MRP and JIT. Requires ERP experience (preferably SAP) and strong analytical and collaboration skills.

Seeking a Senior Specialist for the Key Account Management Emerging Technology Team within Animal Health. The role focuses on identifying, shaping, and supporting the delivery of innovative, data-driven solutions to create measurable value for Global Key Accounts. Responsibilities include market analysis, project delivery coordination, stakeholder management, and developing customer-facing materials. The role emphasizes leveraging data insights for animal welfare and operational efficiency.

This role is for a Health Care Systems - Integrated Account Leader responsible for managing business relationships with assigned customer accounts, focusing on product access, sales optimization, and contract performance. The role involves understanding customer needs, building relationships with senior leadership, and developing strategic account plans. It requires experience in managed care, business acumen, strategic planning, and negotiation skills.

This role is responsible for building and sustaining strong, long-term partnerships with key customers in the GB poultry industry. It involves developing and executing account plans to drive sustainable growth, while supporting animal welfare and responsible medicine use. The role requires close collaboration within the Poultry Species Team and cross-functional groups, leveraging a deep understanding of customer needs and the company's biopharmaceutical and technology portfolio.

The Quality Lead at Merck is responsible for technical, operational, and strategic quality oversight of a large molecule drug substance and drug product pipeline. This role ensures compliance with cGMPs and worldwide regulations, provides assessments on compliance status and risk posture, supports capacity planning and financial goals, and may supervise staff. The position requires strong understanding of pharmaceutical quality systems and regulatory requirements.

This role is for a Director of Global Clinical Supply Planning at Merck, responsible for managing the end-to-end clinical supply chain for human health clinical trials. The role involves planning, sourcing, labeling, packaging, and delivering clinical supplies globally, ensuring timely, compliant, and cost-effective availability of investigational medicinal products (IMPs) and comparators within a GxP-regulated environment. It requires leadership of a global team, collaboration with various internal and external partners, and adherence to GMP and company policies.

Merck is seeking a Director, Global Clinical Supply Planning to manage the end-to-end clinical supply chain for R&D. This role involves planning, sourcing, labeling, packaging, and delivery of clinical supplies globally. The Director will serve as the primary GCS point of contact, design strategic and operational plans, and interact with key partner organizations to negotiate timelines and strategies. Responsibilities include establishing manufacturing and release timelines, managing bulk drug supply, identifying supply risks, managing the clinical supply budget, authoring documentation, and supporting metrics collection. The role requires a Bachelor's degree, 8+ years of project management experience, and 5+ years in supply chain planning. Familiarity with SAP, demand planning, GMP, and GCP is essential.

Merck is seeking a senior Quality leader for its Carlow site, responsible for the strategy, governance, and execution of all Quality Unit activities to ensure sustained compliance, inspection readiness, and the reliable supply of high-quality products. The role involves leading Quality Assurance and Quality Control, managing the Quality Management System, overseeing regulatory inspections and audits, and ensuring product disposition in a highly regulated pharmaceutical, vaccine, and biologics manufacturing environment.

This is a legal internship position within Merck's Clinical Research department, focusing on supporting the financial and administrative aspects of clinical trials. The role involves assisting with budget negotiation, contract drafting, patient payment management, and documentation archiving. It is a 12-month internship, with a possibility of extension, and requires a background in legal studies and a Master's in Clinical Research or similar.

Area Manager for Vaccine sales and customer engagement in Hunan, China. Responsibilities include dealer management, market analysis, business planning, customer relationship building (KOLs), ecosystem development, and ensuring compliance with company SOPs and financial policies. Requires 5+ years of experience in the pharmaceutical industry, preferably in sales management or the vaccine sector.

Intern role in Medical Affairs at Merck, focusing on supporting medical activities, implementing tactics, coordinating logistics, and engaging with scientific and clinical data. The role involves providing scientific information to internal stakeholders and understanding assigned assets and the healthcare environment.

The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports, case management, and ensuring compliance with regulatory requirements in the healthcare domain.

Director of Technical Product Management at Merck, focused on building foundational data capabilities for the Research division to support scientific discovery and drug development. The role involves designing and operationalizing data integration, data modeling, master data management, and ensuring data quality within a regulated scientific environment.

The Safety Data Lead role at Merck is responsible for analyzing and interpreting adverse experience reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes. This involves data entry, case management, and collaboration with stakeholders to resolve issues and optimize processes within the pharmacovigilance domain.

The Safety Data Lead analyzes and interprets adverse experience reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes. This role involves data entry, case management, and collaboration with stakeholders to resolve issues and optimize processes within the pharmacovigilance domain.

The Safety Data Lead role at Merck focuses on the analysis, interpretation, and data entry of adverse experience (AE) reports for investigational and marketed products. This position requires compliance with regulatory requirements and internal processes, collaboration with stakeholders to resolve issues, and support for optimizing case management activities. The role operates under the supervision of a GPVCM Manager and involves applying clinical knowledge and understanding of pharmacovigilance processes.

This role supports the Global Sourcing Management Group (GSMG) by driving sourcing and contracting process excellence, policy adherence, compliance governance, and audit readiness. It involves partnering with stakeholders across GSMG and cross-functional groups like Legal, Finance, Global Compliance, and Audit teams to ensure efficient, compliant, and scalable Procurement operations. Key responsibilities include supporting global sourcing and contracting activities, optimizing processes and systems, assisting with policy implementation, and acting as a point of contact for procurement-related audits.

The Safety Data Lead is responsible for analyzing and interpreting adverse experience (AE) reports, managing cases for investigational and marketed products, and collaborating with stakeholders to ensure compliance with regulatory requirements and internal processes within the pharmacovigilance domain.

This role is responsible for the registration, maintenance, labeling, and compliance of assigned pharmaceutical products in alignment with local and regional regulatory requirements. It involves building relationships with health authorities and internal stakeholders to ensure timely approvals and ongoing compliance.

Account Manager for Companion Animal products in the UK, responsible for sales growth, customer relationship management, and launching new products. Requires a strong sales background, commercial thinking, and customer-centric behaviors.

The GPM Data Analyst role at Merck focuses on master data management and governance within the Central Data & Analytics Office. Responsibilities include processing various data files (formulary, price, diagnosis codes), managing market definitions, supporting product launches, and participating in the Systems Development Lifecycle. The role requires collaboration with business, operations, and IT stakeholders, ensuring data quality and timely delivery of critical product information for sales, marketing, and analytics use cases. Experience in data management, sales/marketing operations within the biopharmaceutical industry, and familiarity with tools like Informatica MDM and SQL are preferred.

Merck is seeking a Regulatory Affairs Coordinator to manage product registration, ensuring market approval and distribution compliance. This role involves coordinating documentation for new registrations, renewals, and post-approval changes, maintaining regulatory databases, and ensuring alignment with local and international regulations and Good Manufacturing Practices. The position also requires managing artwork approvals, supporting tender bids, and ensuring product licenses remain compliant.

Associate Director of Business Development & Licensing (BD&L) Discovery Transactions for Merck, focusing on negotiating agreements for research collaborations and partnerships in the discovery and preclinical stages of drug development. Requires a scientific background and experience in transactions within the pharmaceutical or biotech industries.

Product Owner for Active Data Management at Merck, focusing on designing and implementing a Live Archiving product to manage electronic data at the end of its production cycle, ensuring compliance with data retention obligations and driving cost savings.

Merck is seeking a Production Planning Controller for a fixed-term position in Joinville, Brazil. The role involves managing production processes, optimizing resource utilization, and ensuring efficient operations. Key responsibilities include production planning, inventory control, data analysis, interdepartmental collaboration, and participation in S&OP processes. The ideal candidate will have experience with ERP systems (preferably SAP), knowledge of MRP and JIT, and strong analytical and communication skills. This role is crucial for aligning production with market demands and maintaining operational efficiency within the pharmaceutical industry.

This role is a Specialist in Change Control at Merck, a healthcare company. The primary responsibility is to manage and implement changes within manufacturing operations, ensuring alignment with production, engineering, quality, and regulatory requirements. The role involves project management for change implementation, coordination of resources, monitoring supplier changes, and ensuring compliance with regulations like FDA, EMA, and cGMP. It requires strong organizational, communication, and risk-based decision-making skills, with a focus on maintaining product supply and documentation accuracy.

This role leads the front-end of strategic discovery within a global healthcare biopharma company. The Senior Specialist, Business Experience Architect will dive into business problems, uncover pain points, identify value, and translate insights into clear business opportunities. Responsibilities include conducting discovery across business functions, facilitating workshops, mapping current-state experiences, identifying value opportunities, and preparing discovery briefs for enterprise architects and design teams. The role requires strong business analysis, user empathy, workshop facilitation, stakeholder management, and experience with Design Thinking or similar methodologies. It focuses on understanding and connecting business capabilities, platforms, data, and integrations end-to-end, and articulating measurable business outcomes.

This role supports Medical Operations within the Global Medical Affairs Capabilities Hub at Merck, focusing on communication, meeting organization, and execution of Medical Operations initiatives. It involves supporting tools like X-Fly insights, managing the Country-to-Country (C2C) program, creating reports, and collaborating with global and country-level teams. The position requires a Bachelor's degree, 5+ years of Medical Affairs experience, strong English proficiency, and expertise in Microsoft Office Suite. Key responsibilities include supporting strategic initiatives, ensuring compliance with SOPs and regulations, and acting as a subject matter expert in V&I systems. The role demands strong organizational, problem-solving, and analytical skills, with an emphasis on adaptability and detail orientation within a complex, regulated environment.

This role handles adverse drug events and technical product inquiries for companion animal products, involving case review, trend analysis, and training. It requires a DVM/VMD degree and experience in veterinary medicine, with a focus on pharmacovigilance and compliance within the pharmaceutical industry.

This role is for an Oncology Key Account Manager in Urology at Merck, focusing on managing relationships with large community urology group practices. The primary responsibilities include building trust, understanding the product portfolio and treatment decision factors, utilizing data analytics for account performance, and developing strategic account plans. The role requires strong leadership, clinical proficiency, business acumen, and operational account management skills. The target geography covers 8 states in the Great Plains, with significant travel required. Minimum requirements include a Bachelor's degree or equivalent experience, with at least 2 years in the healthcare/life sciences industry, sales, or account management. Preferred qualifications include an advanced degree and local market relationships in oncology-urology.

This is an Accounting Intern position at Merck, focused on assisting with daily accounting tasks, financial reporting, and preparing financial statements within the pharmaceutical industry. The role requires proficiency in Microsoft Office and basic accounting concepts.

This is an internship position for a life science master's student at Merck, focusing on Global Clinical Trial Operations. The role involves supporting clinical research, gaining practical experience, and contributing to projects within a data-driven environment.

This role focuses on advancing patient care through high-quality, independent, and evidence-based medical education. The Associate Director evaluates IME grant proposals, ensuring alignment with educational needs, therapeutic area priorities, and scientific integrity. They collaborate cross-functionally to ensure educational investments are strategically focused, compliance-appropriate, and improve clinical practice.