Merck

Internship program at Merck focused on supporting HR functions including onboarding, communications, special projects, and talent acquisition. Requires students pursuing degrees in HR, Labor Relations, Psychology, or Communications with at least 1.5 years remaining until graduation. Intermediate/advanced English is highly desirable.

Senior Director role in Regulatory Affairs at Merck, focusing on developing and implementing global regulatory strategies for General Medicine programs, particularly in cardiovascular/renal/respiratory therapeutic areas. The role involves acting as the Global Regulatory Lead (GRL), interacting with global health authorities like the FDA, and overseeing regulatory submissions and approvals throughout the drug lifecycle.

Director, US Market Access Payer Contracting role at Merck, responsible for leading a team to achieve profitable product access through contract management, negotiation, and implementation with national and regional health plans and PBMs. Requires deep customer knowledge, analytical acumen, and cross-functional collaboration to manage the end-to-end contract lifecycle.

Associate Director of Ophthalmic Learning & Development responsible for designing and executing strategic learning plans for product launches and ongoing commercial learning. This role involves defining learning strategy, developing curricula, establishing measurement frameworks, and partnering with cross-functional teams to ensure learning drives business outcomes. The role also includes managing a team of L&D professionals and providing thought leadership on adult learning principles and digital enablement.

Executive Director role leading the regulatory review of promotion and advertising materials for pharmaceutical products in the US. Requires extensive experience in biopharmaceutical industry compliance, regulatory strategy, and promotion development, with a strong focus on US prescription drug advertising and promotion review. The role involves managing a team, liaising with the FDA, and partnering with commercial, medical, and legal teams to ensure compliant and impactful promotional campaigns.

Scientist role focused on establishing and maintaining laboratory automation and robotic systems for high-throughput analytical assays in vaccine research and development. Responsibilities include performing automated biochemical, immunoassay, and cell-based methods, troubleshooting technical issues, maintaining lab equipment, and executing method development, qualifications, and validations. Requires experience with liquid handlers, robotic systems, and software, as well as working in a regulated laboratory environment.

This is a field-based account management role for Merck's vaccine division, responsible for leading vaccine growth strategy, managing key customer relationships, and driving business performance within a designated market. The role requires deep knowledge of the vaccination landscape, competitor analysis, and cross-functional collaboration to ensure compliant solutions and identify growth opportunities.

The Medical & Scientific Liaison (MSL) role in Oncology at Merck focuses on engaging with Healthcare Professionals and Researchers to provide scientific and therapeutic information. The role involves in-depth scientific exchange, knowledge transfer initiatives, and supporting the development and execution of the Oncology Medical Affairs Plan. Key responsibilities include managing budgets, providing medical/scientific advice to internal teams, and supporting regulatory reporting. The position requires a PhD or equivalent, at least 2 years of MSL experience, and strong knowledge of oncology and pharmaceutical industry standards.

Associate Director, Engineering role at Merck focused on managing maintenance staff for Infrastructure Maintenance, Vaccine, and Biologic or Antibiotic Sterile operations. The role is responsible for improving asset reliability and manufacturing capacity through maintenance and technical support, ensuring compliance with GMP, Safety, and Environmental regulations. Requires a Bachelor's degree in Engineering or related field with at least ten years of experience in Maintenance or Utilities Operations, including supervisory experience and expertise in predictive/preventive maintenance programs. Experience in regulated pharmaceutical environments and with CMMS implementations is preferred.

This role is for a Senior Analyst in Order to Cash at Merck, managing the end-to-end order process, customer requests, and internal coordination. It involves order capture, fulfillment, delivery confirmation, and post-delivery support, with a focus on accuracy, timeliness, and customer satisfaction. The role also includes processing credits/debits, assisting with claim disputes, and driving process improvements within the SAP environment.

This role is for a Regional Medical Scientific Director at Merck, focusing on the COPD program. The position involves engaging with Scientific Leaders to exchange scientific and medical information, supporting clinical trials, and gathering scientific insights. The role requires a PhD or equivalent, significant therapeutic area experience, and a strong understanding of regulatory guidelines like HIPAA.

Merck is seeking a Vence Field Application Specialist to act as the R&D frontline for Vence customers, focusing on designing, configuring, and optimizing virtual fencing solutions on farms and ranches. This role involves contributing to field testing strategy, executing field trials, owning R&D-driven field investigations, and translating field outcomes into actionable R&D insights. The position requires strong analytical and problem-solving skills, experience with complex HW/SW systems, and the ability to work independently in the field while collaborating with cross-functional teams.

Seeking a scientist with expertise in mass spectrometry-based protein, protein conjugation, or oligonucleotide/polysaccharide characterization, with strong proteomics and data science skills, to support vaccine programs. Responsibilities include conducting experiments, developing new methods, processing data, and documenting findings.

The Lab Specialist Quality Control at Merck's Animal Health division in Boxmeer, NLD, is responsible for supporting quality control testing of vaccines and pharmaceutical products. This role involves performing physical, chemical, biological, and microbiological tests, trend analysis, and continuous process improvement using Lean/Six Sigma tools. Key responsibilities include acting as a knowledge holder for analytical chemistry techniques, supporting tactical and strategic team leads, leading or participating in projects related to corrective actions, improvements, validation, and calibration, and serving as a point of contact for deviations, changes, audits, and training according to GMP procedures. The role also involves conducting complex root cause analyses for deviation management and site audits. A minimum of a HBO degree in a laboratory field (preferably analytical chemistry) and at least 2 years of specialist experience in a GMP environment are required, with a preference for experience in an analytical chemistry QC lab or pharmaceutical production setting. Strong English and Dutch communication skills and experience with Change and Project Management are also necessary.

Director of Global Media Relations at Merck, responsible for shaping and executing a global media strategy to elevate the company's scientific leadership, pipeline progress, product milestones, and corporate reputation. This role involves building relationships with journalists, anticipating news cycles, and positioning the company through storytelling and rapid response. The director will partner with various internal departments, manage media response plans, and communicate complex ideas effectively. A deep understanding of the company's science, products, pipeline, and the healthcare/pharmaceutical landscape is required.

Executive Director, Clinical Operations, Oncology role at Merck, focusing on strategic planning, management, and execution of HQ-sponsored clinical trials within the Oncology therapeutic area. Requires extensive experience in clinical development programs and leadership in cross-functional initiatives.

Software Engineer role in Finance IT at Merck, an entry-level position focused on developing and supporting enterprise applications for Finance teams. The role involves implementing features, working on integrations, participating in code reviews and testing, and troubleshooting issues. Requires strong technical aptitude, problem-solving skills, and experience with Git and at least one programming language. Exposure to cloud platforms and finance systems is preferred.

Scientist in Biologics Process Research & Development (BPR&D) at Merck, focusing on developing innovative and robust manufacturing processes for biotherapeutics. This role involves experimental design, process development, and collaboration across various scientific and manufacturing functions, with a potential to integrate digital tools for process design.

Product Line Lead for Contract Lifecycle Management (CLM) software, focusing on strategy, roadmap, and delivery of enterprise-scale solutions. Requires strong product management, stakeholder engagement, and delivery leadership skills, with experience in SaaS platforms and collaboration with Legal, Procurement, and Compliance.

This role focuses on maintaining and enhancing technologies for Data Analytics Catalog and Data Management (MDM/RDM) using tools like Collibra and Informatica MDM. The engineer will develop, configure, and maintain software for these platforms, configure AWS using IaC, and collaborate globally to optimize data connections and share best practices. The position requires experience with Python, AWS, REST/Graph APIs, SaaS configuration, DevOps, and CI/CD practices.

Recent graduate opportunity in Global Data Operations at Merck, focusing on clinical data management. Requires a degree in Biomedical Engineering, Bioengineering, Microbiology, or related fields, with 2 years of work experience. Emphasizes data cleaning, management, analysis, and visualization within a healthcare context.

This role is not AI-related as it focuses on global sourcing and contracting within a biopharmaceutical company. The responsibilities include planning capacity, managing projects, contract management, and risk assessments, with required skills in business, finance, and supply chain management. AI/ML is not a core component of this position.

This role is for a Technical Scrum Master at Merck, focusing on Enterprise Information Technology (EIT) within the Treasury product and finance value team. The primary responsibilities include orchestrating Treasury applications, managing interfaces and capabilities, resolving production issues, supporting release management, and leading Agile ceremonies. The role requires experience in IT program and product management, Agile practices, and strong leadership and problem-solving skills.

Werkstudent (m/w/d) role in Patient Engagement at Merck in Munich, focusing on supporting patient engagement projects, internal communication, data maintenance, and research. Requires a student in Pharmacy, Medicine, Natural Sciences, Public Health, or Political Science with a passion for patient collaboration and strong analytical and organizational skills.

The Improvement Officer at Merck's Animal Health division in Boxmeer, Netherlands, is responsible for optimizing production processes for vaccines and pharmaceuticals. This role involves data analysis to drive decision-making, identifying and solving structural problems, managing improvement initiatives, and facilitating kaizen workshops. The position requires a Bachelor's or Master's degree in a relevant field and experience in data analysis, process improvement, and project management within a production environment.

Manager responsible for overseeing and managing all engineering and maintenance activities within a facility, ensuring production operations run smoothly, managing budgets, and fostering a culture of continuous improvement. The role requires strong leadership, project management, and regulatory compliance skills, with a focus on maintaining facilities and equipment.

This role is responsible for the archival and lifecycle management of electronic records within a Records Management Center of Excellence (RM CoE). Key responsibilities include performing annual reviews and clean-up of archived data, supporting data retrieval requests, maintaining electronic repositories, contributing to data migration and archival projects, and producing project reports. The role requires experience in the pharmaceutical or regulated industry, familiarity with reporting tools, computer systems validation, and document control management.

Team leader for packaging operations at a Merck Animal Health facility in Boxmeer, Netherlands. Responsible for managing a team of 15-20 operators, ensuring productivity, quality, and safety in vaccine packaging. The role involves analyzing daily results, resolving recurring issues, translating policy into operational plans, and fostering team autonomy. Requires a Bachelor's degree (Technical, Pharmaceutical, or Business), leadership experience in production, and ideally GMP experience. The role is shift-based.

Logistics Operator role at Merck in Boxmeer, Netherlands, focusing on managing incoming and outgoing goods for the Formulation and Filling Department. Responsibilities include inventory management, adherence to GMP/GDP guidelines, and ensuring product safety and hygiene. Requires MBO 3 education, experience with SAP, and availability for a five-day work week with occasional Saturdays. A forklift certificate and GMP/GDP experience are preferred.

The Site Digital Technology Lead is responsible for coordinating IT/OT operations at a specific site, ensuring alignment with business goals and global IT/OT strategy. This role involves managing local IT teams, driving digital transformation, implementing projects, managing budgets, and ensuring compliance with regulatory, safety, and cybersecurity requirements. The position requires experience in IT/Automation leadership, digital transformation, and stakeholder management within a matrix organization.

Principal Scientist in Biologics Analytical R&D at Merck, focused on defining analytical strategy and leading a team to solve complex analytical problems in biologics API development. Requires extensive experience in biologics analysis, assay development, and regulatory filings.

This role is part of the COSI (Cost of Sales & Inventory) organization, responsible for end-to-end accounting activities for inventory throughout the supply chain. The Senior Specialist will maintain, review, report, and analyze inventory, intercompany profit, production, and product cost data to support monthly accounting close and management cycles for one or multiple plants. Responsibilities include maintaining product costs per US GAAP, controlling and analyzing production results, ensuring accurate data reporting, analyzing in-transit inventory, and preparing annual profit plans.

Clinical Data Management Analyst responsible for executing end-to-end data management activities for clinical trials, including tool development, data collection, integrity review, query management, medical coding, and database lock preparation, in compliance with SOPs and guidelines.

Associate Scientist in Biologics Process Research & Development (BPR&D) at Merck, focusing on designing, developing, and executing robust processes for biological products. The role involves contributing to innovative manufacturing technologies, conducting experiments for unit operations, and collaborating across R&D and manufacturing teams. Experience with bioprocessing, cell culture, protein purification, and data analysis is required.

This role at Merck focuses on Biologics Process Research & Development (BPR&D), aiming to efficiently develop innovative and robust manufacturing processes for biotherapeutics. Responsibilities include developing disruptive technologies, applying scientific principles to solve process development challenges, designing and conducting lab/pilot-scale studies, and collaborating with cross-functional teams. The role requires a Bachelor's, Master's, or PhD in a relevant scientific or engineering field with several years of experience, and proficiency in experimental design, data analysis, and problem-solving. Experience in upstream or downstream bioprocessing is essential. While AI/ML is mentioned as a preferred skill, the core of the role is in bioprocess development, not AI/ML model building.

Merck is seeking a DevOps Squad Lead to build core components for their Research Labs' data analytics, visualization, and management workflows. This role involves developing and supporting large-scale data processing pipelines and analytical workflows on HPC infrastructure, managing scientific data at scale, and ensuring regulatory compliance. The lead will also promote DevOps best practices and manage technical dependencies to deliver impactful solutions for drug discovery.

Operations Director for Biologics clinical and commercial manufacturing, responsible for capacity realization, operational excellence, and leading manufacturing teams and processes. The role involves technology transfer, PPQ, inspection readiness, and ensuring compliance with regulatory expectations. It emphasizes Lean principles, continuous improvement, and developing a strong technical and digital mindset within the department.

This role focuses on statistical programming for PK modeling and simulation in the Oncology therapeutic area at Merck. Responsibilities include data gathering, transformation, dataset creation, and generating tables/figures for reports and regulatory submissions, ensuring programmatic traceability and supporting programming standards. The role requires significant SAS programming expertise in a clinical trial environment.

The Sterile Product Development (SPD) group is responsible for developing non-oral dosage forms (injections, implants, inhaled, ocular) for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. This role supports the Biologics team within SPD, focusing on developing robust composition, primary packaging/device, and process selection through fundamental understanding and characterization. The candidate will lead and contribute to new, innovative approaches for biologics sterile product development, including experimental design, execution, and data analysis, supporting both early and late-stage development candidates. Responsibilities include building fundamental knowledge, providing strategic and technical leadership on program development teams, interfacing with stakeholders, collaborating across functions, leading project activities at external manufacturing sites, and enhancing the company's image through patents, presentations, and publications. The role requires a Ph.D. or Master's/Bachelor's degree with relevant industry experience, expertise in biologics process development and characterization, formulation development, and a strong track record in product development and regulatory filings.

Product Leader for Biologics Value Chain Management at Merck, responsible for end-to-end supply chain ownership, strategy definition and execution, cross-functional alignment, and lifecycle management for biologics products. Requires deep experience in biologics operations, supply chain, and leadership skills to manage complex strategies, risks, and stakeholder engagement.

The Principal Scientist in Outcomes Research will plan and manage real-world evidence and non-interventional research for lung cancer products. This role involves designing studies, developing protocols, analyzing data, and creating dossiers for payers and HTA agencies, aiming to ensure patient access and improve health outcomes.

Principal Scientist role at Merck focused on the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics. Responsibilities include process scale up, technology transfer, process validation, authoring regulatory submissions, and supporting manufacturing investigations. The role requires expertise in sterile drug product fill finish operations and commercialization of biologics programs.

This role is for a U.S. Director of Medical Affairs for COPD at Merck. The position focuses on driving scientific excellence, managing medical affairs plans, and optimizing field readiness within the Value & Implementation organization. Responsibilities include developing regional strategies, contributing to the U.S. Medical Affairs Plan, leading training programs, and ensuring scientific exchange aligns with global communications. The role requires an advanced degree, significant medical affairs and COPD experience, strategic planning abilities, and an AI-first mindset for leveraging AI tools without deep technical expertise.

The Product Owner will drive the evolution of a data marketplace experience, connecting data producers and consumers across the enterprise to enable a thriving ecosystem where data products are shared, consumed, and valued. This role requires product management excellence, understanding of data marketplace dynamics, and building experiences that drive adoption and trust.

Key Account Manager for Merck's EURAM AQUA region, focusing on Norway, Iceland, and Faroe Islands. Responsibilities include identifying and developing new sales opportunities for Pharmaceutical and Welfare solutions, managing key accounts, building relationships with stakeholders, acting as a product expert, and achieving sales targets. Requires a university degree, 3+ years of aquaculture production experience, strong commercial acumen, and sales/key account management experience.

This is a Key Account Manager role in the Vaccines division at Merck, focused on driving revenue growth and portfolio adoption within assigned key accounts in Finland. The role requires deep understanding of the Finnish healthcare ecosystem, commercial sales ownership, account planning, negotiation, and cross-functional execution to achieve sales results. While the role mentions leveraging digital tools and AI-enabled technologies, the core responsibilities are in commercial sales and account management, not AI/ML development.

Merck is seeking a Senior Clinical Research Associate (srCRA) to execute high-quality clinical trials, manage site performance and compliance, and contribute to the development of clinical research territory. The role requires fluency in Norwegian and English, strong knowledge of clinical research guidelines, site management skills, and advanced IT proficiency. The position involves approximately 50% travel.