This role is for a Specialist in Manufacturing Automation Engineer at Merck, focusing on the DeltaV control system. The primary responsibilities include implementing automation change controls, supporting new product introductions, analyzing business requirements for automation software, and ensuring system installations align with company standards. The role also involves system administration, troubleshooting, and documentation updates within a regulated pharmaceutical environment.

This role is responsible for planning and executing clinical-trial biomarkers, focusing on compliant and efficient biospecimen collection, assay execution, and data delivery within the Immunology and Oncology therapeutic areas. The Senior Scientist will partner with scientific and operational colleagues to ensure high-quality biomarker data for clinical trials and translational research.

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.

Associate Specialist, Engineering role at Merck focused on providing end-to-end automation engineering support for sterile drug product cGMP clinical supply manufacturing facilities. Responsibilities include implementation, validation, lifecycle management, and troubleshooting of process automation and OT/IT systems, ensuring reliable and compliant operations. The role supports both startup operations and new capital investments, requiring collaboration with various information and engineering teams.

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.

This role provides end-to-end automation engineering support for a clinical supply manufacturing facility, focusing on non-sterile products. It involves ensuring the reliable and compliant operation of process automation and OT/IT systems, supporting new capital investments, and managing the automation lifecycle. The role requires expertise in cGMP, validation, troubleshooting, and collaboration with various teams, with a need for off-shift work on an intermittent basis.

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.

This role supports global clinical trial operations within Merck's Human Health division, focusing on regulatory affairs. The intern will gain experience in clinical trial regulatory frameworks, Good Clinical Practices, and interactions with regulatory agencies. Key tasks include administrative support for regulatory submissions, monitoring dossiers, reviewing documents, coordinating information, editing informed consents, and participating in process improvement initiatives. The role requires a university degree in Pharmacy or Biochemistry and intermediate English skills.

This role supports and executes mission-critical Government Pricing, Medicaid, and regulatory pricing technology initiatives within the US Market Access organization. It partners with Finance, Compliance, Audit, and Legal to ensure accurate, compliant, and auditable pricing calculations and system behavior. The role involves hands-on ownership of regulatory technology solutions across various platforms, from requirements through production stabilization, and routinely supports external audits, restatements, and issue resolution. While the role mentions working in an AI-assisted environment, its core function is in regulated pricing technology delivery and support, not AI/ML model development.

Principal Scientist role in Oncology In Vivo Pharmacology at Merck, focusing on directing reverse-translational activities, leading drug discovery projects, building alliances, championing new technologies like spatial biology, and collaborating with cross-functional teams and external partners. Responsibilities include performing preclinical experiments, managing external studies, leading a team of scientists, and representing the department in governance forums. Requires a PhD or MS/BS with extensive experience in Oncology drug discovery and in vivo pharmacology, with specific skills in preclinical models, spatial biology, and team management.

HVAC/Refrigeration Technician responsible for installing, maintaining, operating, calibrating, repairing, and troubleshooting refrigeration, air conditioning, and air volume equipment and associated control systems in a pharmaceutical manufacturing environment. Ensures compliance with operating procedures, company, and government regulations, including cGMP. May involve some responsibility for maintaining business systems like CMMS and assisting with planning and scheduling.

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.

Specialist, Automation Engineering role at Merck supporting clinical manufacturing automation systems in a GMP environment. Responsibilities include maintaining validated systems, troubleshooting issues, managing change control, and ensuring compliance with cGMP, data integrity, and cybersecurity requirements. Requires a Bachelor's degree and 2+ years of experience in process automation.

The Procurement Analyst (Mid-Level) will be responsible for supporting sourcing and supplier management processes for services, ensuring efficiency, competitiveness, and alignment with company strategies. This role involves cross-functional collaboration with local, regional, and global stakeholders, contributing to value creation and strengthening procurement governance.

The Associate Specialist, Operations role at Merck is focused on hands-on assistance for daily production activities in a GMP manufacturing facility. This includes equipment setups, raw material sampling, solution preparations, batch processing, and troubleshooting, all while ensuring compliance with Safety & Environmental and cGMP requirements. The role supports process development, technology development, and the supply of Active Pharmaceutical Ingredient (API) for clinical use. It involves both wet chemistry and dry powder processing, with a primary focus on executing batch production work and contributing to facility improvement activities.

This role supports the transfer, implementation, and ongoing management of Quality Control (QC) methods and processes within Merck's Animal Health Division. It involves hands-on laboratory work, project coordination, and quality oversight to ensure compliance with USDA regulations and internal quality standards, particularly during a site expansion project. The specialist will collaborate with cross-functional teams, manage test methods and specifications, conduct gap and risk assessments, and support investigations and training.

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.

Seeking a Senior Scientist in Stromal Immunology to work in a lab-based role, evaluating and applying novel experimental approaches to identify and validate therapeutic targets for inflammatory and autoimmune diseases. The role involves designing and executing experiments, analyzing complex datasets, and contributing to the development of new therapies.

This role focuses on developing downstream purification processes for biologics pipeline, optimizing unit operations, and leveraging data science for complex problem-solving within the healthcare domain. It involves collaboration, technical supervision, and strategic process development.

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.

Internship opportunity within Merck's Discovery & Technology department focused on improving a cell line for viral antigen production. The role involves combining molecular techniques with pilot scale cell culturing to create an in vitro cell substrate for high antigen yields in large-scale manufacturing. The intern will execute experiments, troubleshoot, and document findings, contributing to vaccine development.

Distinguished Scientist (Executive Director) at Merck, leading clinical research for oncology indications and vaccines. Responsibilities include planning, directing, and overseeing the entire clinical development cycle, from study design to regulatory reporting and publication. The role involves managing cross-functional teams, interacting with key opinion leaders, and maintaining scientific knowledge in the field.

Junior Veterinary Researcher role focused on conducting research studies for veterinary drug development, including study planning, execution, and reporting, while adhering to GLP/GCP guidelines. Responsibilities also include sample processing, financial administration, and lab equipment maintenance.

Seeking a scientist focused on device characterization and design for drug delivery platforms, involving technical interrogation, risk identification, and improvement opportunities. The role utilizes analytical instruments and methodologies, including in silico modeling, for understanding device material and functional properties, particularly for intravitreal injection combination products. Requires strong cross-functional collaboration, scientific leadership, and communication skills.

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.

Principal Scientist role focused on downstream process development for biotherapeutics at Merck. The role involves designing purification processes, developing technical strategies, and innovating manufacturing technologies. It requires collaboration with cross-functional teams, publishing research, and mentoring staff. While AI/ML is mentioned as a preferred skill, it is not the core craft of the role.

Staff Reliability Engineer role focused on implementing and operationalizing reliability practices, ensuring systems are designed, built, and operated with reliability in mind. This role partners with engineering teams to embed reliability into system design, development, and operations, supports SLO implementation, and improves observability coverage. It also involves developing automation for incident response and leveraging AI-enabled capabilities where appropriate.

This role focuses on scaling Linux/Unix infrastructure operations through automation, observability, and AI-assisted practices. It requires deep Linux/Unix expertise, infrastructure engineering discipline, and leadership to drive continuous improvement and ensure sustainable production operations. The role emphasizes converting operational knowledge into automated capabilities and embedding security by design.

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.

Automation Engineer role at Merck's vaccine facility, focusing on supporting and improving OEM automation systems (Siemens, Rockwell) in a GMP-compliant environment. Responsibilities include technical support, problem resolution, system design, commissioning, qualification, validation, and implementing digital/paperless solutions. Requires a bachelor's degree, 3+ years in a regulated industry, and experience with PLC automation systems.

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.

Internship role in Process & Support Operations at Merck, focusing on supporting early-phase clinical therapies manufacturing. Responsibilities include operational support, administrative tasks, data entry, GMP/EHS standards adherence, material handling, and continuous improvement tasks within a manufacturing environment. Requires a Bachelor/Master's degree in a relevant discipline and proficiency in MS Office and German/English.

Senior Manager for Network Automation Developer role at Merck, focusing on designing, developing, and maintaining software systems for network management and services. The role involves Python, AWS, GIT, networking, Ansible, Terraform, and CI/CD practices, with a strong emphasis on automation and digital transformation within a healthcare biopharma company.

Merck is seeking a Regional R&D Director for their Ruminants division. This leadership role involves managing, coaching, and developing a team of 13 scientists in Boxmeer, NL. The director will be responsible for biological research and development, leading to the timely launch of commercially viable Ruminants Biologicals. The role requires a PhD in life sciences with significant experience in vaccine development for animal health, proven team management skills, and a results-driven, innovative mindset. Collaboration with global teams in Marketing, Commercial, Manufacturing, Regulatory Affairs, and Legal is essential.

Operational Manager for Global Logistics at Merck in Haarlem, Netherlands. Responsible for safety, quality, and productivity in a warehouse and distribution setting. Manages a team of 10-15 operators, oversees operational processes, ensures adherence to quality standards (GMP/GDP), and leads improvement projects using Lean methodologies. Requires a Bachelor's degree, at least one year of leadership experience, strong people management skills, project management abilities, and experience with SAP and Lean principles.

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.

Process Engineer at Merck's Animal Health division in Boxmeer, Netherlands. Responsible for developing and improving machines and processes, acting as a problem solver in project teams from concept to implementation. Involves root cause analysis, risk assessment, protocol development, and leading improvement initiatives using Lean tools. Requires a technical degree, GMP experience, and at least three years of production environment experience.

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.

Merck is seeking a Senior Specialist, QE Engineer in Hyderabad to lead a Quality Engineering team, build high-throughput testing capabilities, and mentor test engineers. The role involves defining test strategies, building automation scripts (Robot Framework, TOSCA, Load Runner), integrating tests into CI/CD pipelines on AWS, and ensuring adherence to regulatory requirements (GLP/GCP). The candidate will also manage test engineers, oversee testing artifacts, and collaborate with cross-functional teams.