Merck

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.

This role is for a Senior Specialist in SAP Data Engineering at Merck, a global healthcare company. The primary focus is on the design, development, and global rollout of SAP BI solutions, specifically involving SAP BW/HANA. Responsibilities include requirements gathering, technical design, development, testing coordination, and post-go-live support, adhering to SDLC standards. The role also involves contributing to ECC to S/4HANA migration remediation activities within a diverse, globally distributed team. Experience with SAP BW, HANA, data modeling, SQL, and cross-functional collaboration is required, with a strong emphasis on operating in a regulated pharma environment.

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.

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.