This role focuses on technology risk management and cybersecurity within the Animal Health division of a global healthcare company. The Senior Specialist will partner with business and technology teams to identify, assess, and advise on information security and compliance risks, ensuring that security and privacy considerations are integrated into projects and operations. The role involves translating technical risks into business context, supporting risk governance, and contributing to the adoption of security standards, with an awareness of emerging technologies like AI.

Maintenance Technician role focused on performing and documenting routine maintenance, resolving equipment breakdowns, ensuring GMP and legislative compliance, and supporting production schedules within an Engineering Centre of Excellence at Merck.

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.

This role is for a Stamping Process Worker at Merck in New Zealand. The primary responsibility is to operate stamping machines, ensure products meet quality standards, and remove faulty products. The role involves inspecting stamping on tags, adjusting processes, completing production records, maintaining a clean workspace, reporting machine malfunctions, and adhering to safety precautions. Required skills include customer focus, communication, problem-solving, attention to detail, and teamwork. Preferred skills are not specified, but the role is in an animal health organization.

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.

Senior Data Governance Analyst role at Merck, focusing on ensuring data integrity, quality, security, and compliance for commercial and medical affairs data domains. Responsibilities include requirement analysis, stakeholder communication, Collibra DGC environment setup and maintenance, metadata management, and documentation.

This role focuses on engineering and developing Master Data Management (MDM) and Reference Data Management (RDM) solutions, primarily using Informatica IDMC. The engineer will be responsible for designing, developing, and maintaining these products, integrating them with various enterprise systems, and ensuring data quality and governance. The role requires strong data engineering skills and experience within the life sciences 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.

Manager for Quality COE in Lab Support SDLC at Merck, focusing on leading a team of quality specialists for laboratory system qualification, lifecycle management, and ensuring compliance with pharmaceutical manufacturing standards.

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.

Principal Scientist, Drug Discovery role at Merck, focusing on identifying new molecular entities and technologies for animal health. The role involves leading research programs from ideation through early research and proof-of-concept to development, interfacing with internal and external stakeholders. Requires a DVM/VMD and PhD in experimental pharmacology with at least 8 years of industry experience in drug discovery or preclinical research, with expertise in specific therapeutic areas and knowledge of regulatory aspects.

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.

Seeking a Senior Engineer/Scientist to lead the development and implementation of specialized testing methodologies for combination products (e.g., prefilled syringes, auto-injectors, infusers). The role involves test method development/validation, design verification, technical feasibility evaluation, establishing design inputs/outputs, and driving technology transfers. Expertise in medical device and combination product design controls, risk management, and material characterization is required.

Senior Scientist in Biologics Analytical R&D at Merck, focused on developing, qualifying, and troubleshooting analytical methods for therapeutic proteins. Requires a strong background in separations science (UPLC/HPLC, CE) and experience with assay development for release, characterization, and stability testing. The role involves scientific leadership, collaboration, and authoring technical reports and regulatory filings.

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.

This role focuses on generating real-world data and evidence to inform clinical program design, access strategies, and policy for high-priority therapeutic areas, with a specific emphasis on health equity. The Associate Director will lead mixed-methods studies, integrate social determinants of health and patient-reported measures, develop external partnerships, and translate findings into actionable recommendations for clinical protocols, site selection, and policy. The role requires expertise in quantitative and qualitative research methods, data analysis, and collaboration with diverse stakeholders, ensuring research adheres to ethical and regulatory standards.

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.

Senior Scientist role focused on leading animal vaccine development projects from discovery through licensure, involving experimental design, data analysis, cross-functional team leadership, and regulatory compliance within a regulated environment.

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 focuses on designing, implementing, and maintaining the organization's virtualized infrastructure (VMware) and Windows server environments. Key responsibilities include managing virtual machines, Active Directory, Group Policy, and automating tasks using PowerShell. The role requires expertise in VMware and Windows administration to ensure high availability, performance, and security of IT services.

This role focuses on designing, implementing, and maintaining the organization's virtualized infrastructure (VMware) and Windows server environments. Key responsibilities include managing virtual machines, Active Directory, Group Policy, and automating tasks using PowerShell. The role requires expertise in VMware and Windows administration to ensure high availability, performance, and security of IT services.

Associate Principal Scientist role focused on designing, coordinating, monitoring, and reporting clinical laboratory and field studies for companion animal and livestock products, ensuring compliance with GCP and GLP guidelines. The role involves study team leadership, investigator selection, permit applications, and final report preparation, with a strong emphasis on scientific and regulatory requirements within the animal health sector.

This role supports pharmacovigilance activities within the pharmaceutical industry, focusing on ensuring adherence to regulations, managing adverse event cases, and supporting PV processes. It involves collaboration with internal and external parties, local audits, and maintaining PV procedures.

This role is for an Electrical & Instrumentation Technician in a biopharmaceutical manufacturing setting, participating in a two-year training program to develop skills in the industry. Responsibilities include supporting maintenance, inventory management, quality system improvements, vendor coordination, and basic diagnostic of equipment failure.

This role is for a Specialist in Manufacturing Automation Engineer at Merck, a global healthcare biopharma company. The position, based in Hyderabad or Pune, involves supporting DeltaV automation software change controls for worldwide manufacturing sites. Responsibilities include project management, system upgrades, troubleshooting, documentation, and ensuring compliance with GMPs, CSV, safety, and environmental regulations. The role focuses on implementing automation solutions and supporting digital shop floor technologies within the pharmaceutical manufacturing context.

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.

Senior Archivist role at Merck focused on managing and facilitating archival activities for Nonclinical documents and electronic data, ensuring compliance with Good Laboratory Practices (GLPs) and federal regulations. Responsibilities include indexing, filing, retrieval, electronic archival, supporting regulatory inspections, and coordinating standard archival operations.

This role is for a Sr. Director of Epidemiology in Hematology at Merck, focusing on leading a team of epidemiologists to conduct and oversee epidemiologic research for assigned company assets and indications. Responsibilities include scientific oversight, planning, design, and execution of studies related to clinical development, safety, effectiveness, and observational research. The role involves presenting research plans, interacting with regulatory agencies, and managing a team. It requires extensive experience in epidemiologic projects and a strong track record in research publications.

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.

Scientist role at Merck focused on molecular discovery, specifically optimizing next-generation sequencing for in vitro display campaigns to discover and engineer therapeutic candidates. Requires strong molecular biology and NGS understanding, with collaboration across biology, protein engineering, and data science teams.

This role is for a Senior Software Engineer specializing in Kinaxis Maestro to configure and implement supply chain management software. The responsibilities include translating business requirements into software specifications, leading data integration, managing QA/UAT, and coordinating with product engineering. The role requires experience in Kinaxis Maestro, supply chain planning modules, Python, JavaScript, and Agile methodologies.

Merck is seeking a Specialist Production Support in Krems, Austria, to support biopharmaceutical manufacturing. The role involves process transfer, implementation, optimization, and improvement, as well as handling deviations and change management. The ideal candidate has a science degree, experience in GMP manufacturing, project management, and root cause analysis, with strong quality and safety awareness.

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 role is for a Maintenance Lead at Merck's biopharmaceutical facility. The lead will be responsible for managing a maintenance team, ensuring equipment uptime and compliance with GMP standards, and driving continuous improvement projects. The role requires strong people leadership, problem-solving skills, and experience in the pharmaceutical or biotechnology industry.

This role is for an Infrastructure Engineer at Merck, a global healthcare biopharma company. The engineer will be responsible for designing, implementing, managing, and supporting IT infrastructure, including hardware, networking, virtualization, cloud environments, and security systems. The role involves working with VMWare, configuration management tools (Ansible, Terraform), scripting, CI/CD practices, and Git to ensure efficient, reliable, and scalable IT systems. The focus is on supporting the company's digital transformation journey and enabling business outcomes through technology.

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.

Intern role within the Commercial Operations department and Data team at Merck, focusing on the transformation, harmonization, and continuous improvement of data analysis and insights creation using data platforms to deliver actionable business insights. Requires skills in data analysis, Excel, and preferably visualization tools like Power BI.

The Regional Dossier Publisher (RDP) is responsible for publishing key regulatory submissions in the EU+EEMEA region, supporting the publishing work of the regional team. This role requires knowledge of regulatory procedures and dossier requirements, and involves supporting country RA teams with local publishing and submission transmission needs. The RDP will also assist in the development of tools and procedures for submission publishing.

This role is for a ServiceNow Developer responsible for designing, coding, testing, and implementing solutions within the ServiceNow platform to meet ITSM, Service Portal, and Virtual Agent requirements. The developer will collaborate with cross-functional teams, integrate ServiceNow with other systems, and support reporting and analytics.

Associate Principal Scientist role in R&D Clinical Research for General and Specialty Medicine at Merck, focusing on oncology-adjacent areas like General Medicine, Infectious Diseases, and Vaccines. Responsibilities include providing medical expertise to development teams, reviewing documents, leading clinical development plans in Japan in collaboration with US headquarters, engaging with scientific leaders, and supporting academic presentations/publications. Requires an MD with 5+ years of clinical experience in cardiology or equivalent, strong collaboration, English negotiation/speaking/writing skills, and fluent Japanese.

Technical Project Manager responsible for end-to-end project management and delivery of technical deliverables for assigned clinical trials within a specific drug/vaccine program. This includes developing and managing technical project plans from design through production deployment and change management, collaborating with functional areas to secure resources, and engaging with cross-functional stakeholders. The role also involves serving as a point of contact for in-life maintenance, managing change requests, customer expectations, facilitating decision-making, and performing risk management.

Animal Technician role at Merck focused on daily animal care, cleaning, and maintenance of animal facilities. Responsibilities include performing biotechnological procedures with a focus on animal welfare, administering anesthesia, and conducting animal studies. The role requires adherence to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines, accurate data recording, and observation of animal health. Requires an MBO-4 diploma and relevant certifications in animal experimentation. Experience with quality systems like GLP/GMP is preferred.

Associate Director, Engineering role at Merck focused on planning, design, and implementation of capital projects within pharmaceutical manufacturing. This role involves collaboration with various teams, equipment selection, vendor management, and overseeing project execution from start to finish. It requires a strong understanding of GMP manufacturing and project leadership.