Merck

Manager for a Clinical Data Integration team at Merck, focusing on leading end-to-end data integration initiatives to support clinical programs and R&D. The role involves people management, ensuring delivery excellence, and driving continuous improvement in data management processes. Requires experience in data integration, software development, or clinical data management, with a strong emphasis on leadership, quality assurance, and compliance within a regulated healthcare environment.

Scientist, Analytical R&D (Microbiologist) role at Merck focused on performing and analyzing microbiological testing in a GMP environment, including environmental monitoring, utility testing, and finished product testing. Responsibilities include data analysis, investigation support, documentation, and collaboration with stakeholders. Requires a degree in Microbiology or related field with relevant GMP experience.

Merck is seeking a Senior Specialist in Global Engineering Solutions to support Technology Center, Large Molecule Process Engineering. This role involves planning, design, and implementation of capital projects, process & facility design, equipment selection, vendor management, factory acceptance testing, facility start-up, commissioning, construction support, equipment qualification, and technology transfer. The position requires a Bachelor's degree in a relevant engineering field and a minimum of four years of experience in GMP manufacturing or technical support, with at least two years in project leadership. Experience with capital management, downstream process engineering, bioconjugation, and potent compound manufacturing is preferred. The role is project-based and requires on-site support, with flexibility for travel.

This role is for a Senior Scientist in Analytical R&D Microbiology at Merck, focusing on supporting the pipeline through GMP microbiology laboratory work, including finished product testing, utilities, and environmental monitoring. The scientist will build and sustain a scientifically sound, risk-based microbiology program, acting as a subject matter expert in sterile operations and contributing to experimental design, data integrity, and quality investigations.

Associate Scientist role focused on formulation development and manufacturing of sterile pharmaceutical products, from preclinical studies to commercialization. Requires a BS degree in a relevant scientific field and strong collaboration skills. The role involves executing laboratory experiments, data interpretation, and supporting manufacturing operations in GXP environments.

This role focuses on designing and delivering a comprehensive training ecosystem for a new aseptic manufacturing facility, including lyophilization and sterile filling. It involves developing learning pathways for operators and technical staff, aligning training with asset lifecycle phases, and partnering with external education providers. The role requires experience in GMP-regulated environments and technical training program development.

Senior Scientist in Merck's Biologics Analytical Research & Development department focused on solving complex analytical problems at the interface of biology, chemistry, and lab informatics for drug development. Responsibilities include method development, qualification, implementation, troubleshooting, and transfer for monoclonal proteins and other complex therapeutic proteins. Requires strong background in separations science (UPLC/HPLC, CE), assay development, and understanding of Critical Quality Attributes/QbD/DOE principles. Experience with regulatory filings and publications is expected.

Senior Scientist in Biologics Analytical Research & Development at Merck, focused on solving complex analytical problems for drug substance and product development. Responsibilities include method development, qualification, implementation, troubleshooting, and transfer for monoclonal proteins and other complex therapeutic proteins. Requires strong background in separations science (UPLC/HPLC, CE), assay development, and understanding of Critical Quality Attributes. Role involves authoring technical reports and regulatory filings, with a strong emphasis on scientific leadership and collaboration.

Associate Principal Scientist, Microbiology Product Testing Lead AR&D at Merck, responsible for leading microbiology finished product testing, utilities, and environmental monitoring in a GMP environment. Requires extensive knowledge of microbiology laboratory practices, data review, quality procedures, and troubleshooting investigations. The role involves experimental design, execution, data interpretation, method suitability studies, and collaboration with cross-functional teams and Quality stakeholders. Experience with sterile operations, clean room environments, and audit support is preferred.

Director of Toxicology Operations at Merck, managing a team conducting pre-clinical drug safety studies. Requires strong leadership, experience with GLP, and staff development. Focuses on the operational and management aspects of toxicology studies.

This role is an IT professional focused on Audio-Visual (AV) and Conference Rooms Support Specialist with global scope. The position is responsible for the design, delivery, operation, and continuous improvement of AV and conference room services, ensuring a high-quality, customer-centric experience across locations. The Specialist acts as a single point of coordination between onsite IT teams, product teams, vendors, business stakeholders and end users, supporting both hands-on AV operations and service management activities aligned with global strategy.

Manager for Manufacturing Automation in Lab Digital Support Operations, responsible for leading a team, IT support for lab operations, team development, performance management, and strategic goal setting within a regulated healthcare manufacturing environment. Focuses on operational excellence, technology integration, and standardization of lab IT systems.

This role is for a Regional Medical Scientific Director focused on vaccines, engaging with scientific leaders to exchange medical and scientific information, support clinical trials, and gather feedback. It requires an advanced degree (MD, DO, PharmD, PhD, DNP) and experience in vaccines and vaccine-preventable diseases, with a strong understanding of regulatory guidelines like HIPAA.

This role leads the operation, maintenance, and improvement of Building Automation Systems (BAS) for GMP manufacturing and facilities. It involves technical leadership in configuration, programming, troubleshooting, and ensuring compliance with regulatory standards. The focus is on reliable and secure facility automation.

The US Director Medical Affairs (USDMA) is a country medical director role focused on Medical Affairs strategy in Rheumatology and Dermatology. This position drives scientific excellence, optimizes field readiness, and collaborates with cross-functional teams to implement medical affairs plans, including scientific exchange, clinical trials, investigator-sponsored programs, and congresses. The role requires an advanced degree, significant medical affairs and therapeutic area experience, and strong strategic planning, execution, and collaboration skills within the US healthcare system.

This role is for a Senior Specialist - SAP Integration Architect at Merck, focusing on designing and implementing integration solutions using SAP Business Technology Platform (BTP) and other middleware. The candidate will manage interfaces, develop real-time and batch integrations, and ensure compliance with security and regulatory guidelines. The role requires strong experience with SAP PI/PO, SAP Integration Suite, and knowledge of integration patterns and protocols. Experience in a regulated environment is a plus.

This role is responsible for sales forecasting, demand planning, supply management, and product launch/change requirements for an assigned product portfolio within the biopharmaceutical industry. It involves complex modeling, data analysis, cross-functional collaboration, and process improvement.

This role is for a Specialist in Manufacturing Automation Engineer at Merck, focusing on DeltaV control systems for pharmaceutical manufacturing. The responsibilities include developing and implementing automation solutions, managing change controls, supporting system upgrades, troubleshooting, and ensuring compliance with GMP, CSV, safety, and environmental regulations. The role requires experience with Emerson DeltaV system configuration and administration, automation system design, and project execution within the pharmaceutical/life science industry.

The Associate Vice President (AVP), Head of General & Specialty Medicine Clinical Science, is the global functional leader for the General & Specialty Medicine Clinical Scientist (CS) organization within General & Specialty Medicine Clinical Development. This role is accountable for setting scientific standards, operating model, and talent strategy for Clinical Scientists supporting the late stage General & Specialty Medicine portfolio across Immunology, Cardiovascular & Respiratory, Atherosclerosis & Metabolism, and Neuroscience. The AVP ensures that Clinical Scientists deliver consistent, high quality scientific and technical oversight of studies and assets, partnering closely with Clinical Directors (CDs), Product Development Team Leaders, Therapeutic Area Heads, Global Clinical Trials operations teams as well as other cross functional partners to advance programs from First-In-Human through registration and lifecycle management. This role provides horizontal leadership and governance of clinical scientists across the General & Specialty Medicine portfolio.

The Associate Specialist, Process and Instrumentation Engineer role at Merck focuses on developing and maintaining engineering, automation, and calibration teams to ensure high levels of process support and maintainability. This role involves defining key operating parameters, managing the calibration system, documenting processes, and investigating deviations. It requires close collaboration with various departments and supports biological processes for vaccine production. The position emphasizes process definition, critical parameter hierarchy, and regulatory compliance within a regulated environment.

Seeking a Scientific Director for Translational PK/PD, focusing on mechanistic modeling for drug discovery of biologics, protein therapeutics, and peptides. The role involves leading development and supervision of PBPK and QSP modeling strategies, integrating in vitro and in vivo data, and guiding software developers for automated workflows. Requires expert mathematical modeling skills and experience with standard modeling software.

Medical Advisor Oncology role at Merck, focusing on scientific expertise in oncology (onco-dermatology, head and neck cancers), national scientific expert relations, and collaboration with various internal departments. Requires a medical or PhD degree, pharmaceutical industry experience, and knowledge of regulations. The role involves staying updated on literature, engaging with scientific leaders, and ensuring scientific quality of materials.

This role focuses on the development, testing, and validation of analytical methods for veterinary products, involving complex data analysis, bench-level remediation, and authoring regulatory submissions for USDA review. It requires collaboration across various departments and sites to ensure method robustness and successful transfer.

Regional Lead Aseptic Excellence for Merck's Animal Health organization, focusing on sterile manufacturing, microbiology, and contamination control across Europe and Asia Pacific. The role involves leading a team, driving improvement projects, ensuring regulatory compliance, and supporting capital engineering projects.

Seeking a Scientist II to develop and support biofabrication efforts for in vitro microphysiological organ-on-chip systems (MPS) and bioprinted models for drug discovery and development. Responsibilities include hands-on experimentation, cell culture, hydrogel preparation, imaging, and data documentation within a collaborative research environment.

Merck is seeking a Specialist in Pharmaceutical Analytical Sciences to provide hands-on analytical testing support for medical device and combination product development and commercialization. The role involves executing method validation, performing test procedures for clinical supply release and stability testing, and troubleshooting GMP testing challenges. This position requires collaboration with cross-functional teams and adherence to SOPs and ALCOA principles.

Technician role focused on analyzing and resolving technical issues in the pharmaceutical production process, including maintenance, calibration, and validation of equipment. Requires a technical diploma and experience in mechatronics, electrical, or mechanical engineering.

Merck is seeking a Maintenance Technician for Infrastructure at their pharmaceutical production site in Igoville, France. The role involves ensuring the proper functioning and maintenance of infrastructure equipment within a pharmaceutical setting, adhering to strict hygiene, safety, and environmental regulations, as well as Good Manufacturing Practices (GMP). Responsibilities include troubleshooting, preventive maintenance, managing external suppliers, participating in continuous improvement initiatives, and maintaining technical documentation. The position requires a BAC+2 in Maintenance and at least 5 years of industrial experience, with knowledge in electrical, instrumentation, pneumatic, or mechanical systems, as well as fluids, energy, and building systems. Experience in automation is a plus. The role operates on a 2x8 and day shift schedule.

This role is for a Lab Specialist in Quality Control at Merck's Animal Health division. The primary focus is on ensuring accurate test transfers, improving processes, and maintaining compliance with GMP and safety guidelines. The role involves acting as a Quality Control lead for transfer projects and participating in R&D test development.

Senior Pharmacovigilance Specialist role focused on ensuring compliance with local and global PV regulations, managing adverse event handling, aggregate reports, RMPs, and supporting audits/inspections within Merck's UK & Ireland operations.

This role focuses on delivering customer and market insights to business units within the healthcare industry to improve decision-making and optimize promotional strategies. It involves strategic planning, customer/patient mapping, market analysis, sales force effectiveness evaluation, and omnichannel strategy assessment. The role requires strong analytical skills, experience in the pharmaceutical/biotech industry, and familiarity with relevant systems and data sources.

The Senior Scientist, Biopharmaceutics role at Merck focuses on developing and registering new drug products, specifically non-oral dosage forms. The role involves representing the biopharmaceutics team in drug product development, driving biopharmaceutics strategy, and developing next-generation physiologically-based modeling and simulation tools. Key responsibilities include identifying biopharmaceutics risks, influencing formulation strategies, developing quantitative absorption models, and contributing to internal and external innovation in biopharmaceutics and quantitative modeling.

This is an alternating contract (internship) position for a Regulatory Affairs Officer at Merck, focusing on the regulatory aspects of drug lifecycle management. The role involves participating in the preparation and submission of variation dossiers, monitoring evaluations by health authorities, and managing changes to packaging and labeling. It requires a scientific or pharmacy background with a Master's degree in Regulatory Affairs and proficiency in English and relevant IT tools.

Internship role supporting the Digital Gulf team at Merck, focusing on design and video creation projects including logos, websites, emails, and video editing. Requires proficiency in Adobe Creative Suite and strong design/video skills.

This internship role focuses on digital data entry and analysis within the pharmaceutical industry, supporting omnichannel campaigns and developing automation tools for data collection and analysis. It is part of the Digital Gulf team at Merck.

Intern/Co-op role at Merck focused on supporting stakeholder engagement, analyzing travel and meeting spend data, and monitoring data capture accuracy. Requires skills in clinical research, data analysis, reporting, and project management.

Merck is seeking a Planner for their Animal Health site in Boxmeer, Netherlands. The role involves production planning and related tasks for the IVP Filling department, reporting to the Manager Operations. Responsibilities include creating and following production plans, coordinating with internal and external teams, managing personnel and cleaning schedules, and analyzing production data for improvements. The ideal candidate has an MBO 4 education, at least 2 years of experience in a complex production environment (preferably logistics/production planning), and strong Excel and SAP skills. Experience in aseptic or conditioned environments is desired.

Associate Director, Supplier Quality Assurance (SQA) responsible for ensuring the integrity and safety of global API suppliers through strategic oversight, compliance with GMP and global regulations, quality agreements, risk-based assessments, audits, CAPA, QMS strengthening, deviation investigations, technology transfers, process validation, and regulatory interactions.

This is an internship role focused on Sales Force Effectiveness and CRM, involving CRM operations, troubleshooting, event management, database management, and analytics. The role requires fluency in English, ability to work 30-40 hours per week, and a graduation date in Q1 2027 or later. A background in Tech and Computer Science is preferable, along with proficiency in databases and Excel. Key skills include CRM, data analysis, database management, and event management.

Senior Scientist role in Preclinical Development for Animal Health at Merck, focusing on supporting R&D, assessing compound profiles, planning and conducting studies (toxicology, safety, pharmacokinetics, metabolism), preparing regulatory submissions, and collaborating with external experts and project teams. Requires a Veterinary Medicine degree with PhD, experience in R&D within the veterinary pharmaceutical environment, and expertise in pharmacology, metabolism, and toxicology.

Senior Scientist role in Preclinical Development for Animal Health at Merck, focusing on supporting R&D, assessing compound profiles, planning and conducting studies (toxicology, safety, pharmacokinetics, metabolism), preparing regulatory submissions, and collaborating with external experts and project teams. Requires a Veterinary Medicine degree with PhD, experience in R&D within the veterinary pharmaceutical environment, and expertise in pharmacology, metabolism, and toxicology.

The role of a SAP Associate Test Engineer at Merck involves ensuring the quality and functionality of SAP software through meticulous test case design and execution. This includes manual and automated testing, defect identification and documentation, collaboration with developers, and contributing to process improvements. The role requires strong technical skills, SAP module knowledge, and experience with testing tools like TOSCA and JIRA XRAY, particularly within the pharmaceutical industry.

This role focuses on improving and standardizing Environment, Health, and Safety (EHS) processes and safety culture within the Animal Research Department. The specialist will manage the EHS project portfolio, act as a central point of contact for EHS matters, coordinate incident responses, and translate regulations into practical measures. Responsibilities include managing EHS systems, conducting risk analyses, and advising on Biosafety.

Senior Scientist role in Preclinical Development focusing on Immunology for Animal Health at Merck. Responsibilities include scientific support for R&D, compiling and assessing profiles of compounds, planning and evaluating studies (toxicology, safety, pharmacokinetics, immunogenicity), designing and overseeing immunology and monoclonal antibody studies, and compiling reports for regulatory submissions. Requires a Veterinary Medicine degree with a PhD, experience in R&D (preferably veterinary pharma), managing animal studies (GLP), and profound knowledge in pharmacology, toxicology, and immunology. Hands-on experience with immunological assays is essential. Fluency in English and German is required.

This role supports the end-to-end meeting and congress financial process, including vendor and event creation, POs, contract preparation, compliance review, reconciliation, and payments. It requires adherence to company policies and guidelines, collaboration with stakeholders, and process improvement.

Key Account Manager responsible for managing a therapy area, increasing product awareness, answering customer queries, and introducing new products. This role involves reaching out to customers, understanding their needs, and driving prescription sales through effective communication and relationship management with medical practitioners, chemists, and wholesalers. The position also requires achieving sales targets, planning and executing sales strategies, managing key accounts, participating in meetings, and providing guidance to team members. A strong understanding of company products, therapy areas, and competitor products is essential.

This role is for an Oncology Strategic Account Manager in UAE, responsible for achieving territory sales targets, understanding customer needs and market dynamics, and promoting oncology products. It involves cross-functional collaboration and detailed territory planning.