Merck

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.

This role is for a Director of Technology Solutions for a Contract Manufacturing Organization (CMO) within Merck Animal Health. The primary focus is on managing and optimizing the production of electronic and identification products through third-party manufacturers. Responsibilities include building and leading a team, managing supplier relationships, ensuring quality, cost, and delivery, developing risk management processes, and ensuring compliance with industry standards and regulations. The role involves strategic partnerships with CMOs and internal teams to ensure seamless product transitions and continuous improvement in manufacturing processes.

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.

The Safety Data Lead 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 role involves case management, data entry, and collaboration with stakeholders to maintain high-quality and timely execution of pharmacovigilance activities.

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 supports pilot-scale GMP manufacturing of biologics and vaccines, involving upstream and downstream operations, documentation, and process troubleshooting. It requires experience in GMP manufacturing and a strong understanding of regulatory guidelines. The position will temporarily be based in West Point, PA, before relocating to Rahway, NJ.

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.

Associate Director of Tax at Merck, focusing on domestic and international tax planning, M&A due diligence, structuring, and integration. Acts as a liaison between Tax, Business Development, Accounting, and Finance.

Associate Product Manager role at Merck focused on driving growth and delivering performance for assigned products and projects within the pharmaceutical industry, specifically in the Gastrointestinal portfolio. Responsibilities include developing and executing product strategies, leading cross-functional teams, managing marketing campaigns, and ensuring compliance with policies. Requires 5+ years of experience in the pharmaceutical industry, with a proven track record in brand milestones and strong analytical and collaboration skills.

Sales representative for companion animal veterinary products in the Pays de la Loire region of France. Responsibilities include promoting medications, providing training to veterinary professionals, gathering market intelligence, and collaborating with internal teams.

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 for a Senior Specialist, SAP SCM Testing Squad Lead at Merck, a global healthcare biopharma company. The individual will lead a team of testing engineers, develop and execute testing strategies for SAP applications, ensure compliance with international regulatory requirements, and manage testing activities across multiple projects. The role requires experience in SAP modules, testing tools, SDLC in the pharmaceutical industry, and leadership skills.

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.

Technician role in vaccine production, focusing on manufacturing processes in cleanroom environments according to GMP requirements. Responsibilities include operating and maintaining production equipment, preparing and executing manufacturing processes, and ensuring GMP compliance. Experience in aseptic work and GMP documentation is required, with knowledge of cell/virus culture and large-scale equipment being advantageous.

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.

This role supports the conceptualization and implementation of marketing strategies for oncology products, involving brand planning, forecasting, content creation, and campaign execution. It also involves geographic focus, driving business reviews, managing healthcare organizations, and handling international expert programs.

Senior Specialist in Internal Controls & Compliance at Merck, responsible for managing and executing internal control and compliance matters for various operational towers within BSC KL. The role involves control self-assessments, supporting SOX and financial audits, providing expertise, documentation, and training. Requires a Bachelor's degree in accounting or finance, minimum 8 years of audit experience, and experience in a SOX 404 environment.

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.

Seeking a Senior Specialist of Financial Data & Analytics to develop and deliver advanced analytic solutions for strategic decision-making. This role involves partnering with finance SMEs, documenting requirements, supporting end-to-end solution delivery (data modeling, predictive analytics, dashboards), defining master data and security, building forecasting and performance models, and ensuring analytical rigor. The position also requires program and project management within agile methodologies and alignment with compliance (SOX, financial controls).

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.

Manager to lead and coordinate a group of junior and senior project managers, focusing on people management and developing the internal PMO organization. The role involves implementing project initiatives, overseeing the team, tracking capacity, managing projects, and ensuring client satisfaction.

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.

This role focuses on defining and maintaining clinical data standards, ensuring alignment with industry (CDISC) and regulatory requirements within a biopharmaceutical company. It involves data governance, process improvement, and collaboration across various teams and external contacts.

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.

Associate Director, Portfolio Management role within Merck's Finance Digital Office, focusing on governing and advancing digital transformation initiatives. Responsibilities include portfolio intake, prioritization, roadmap management, governance standards, risk identification, executive reporting, process design, and stakeholder engagement. Requires strong financial acumen, project management discipline, and digital fluency.

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.

Automation Engineering Specialist role at Merck supporting sterile clinical manufacturing operations. Responsibilities include maintaining validated automation systems, troubleshooting, implementing platform solutions, managing changes, and representing automation in capital projects. Requires experience in cGMP, quality systems, and PLC/SCADA.

This role provides operational support to the Intellectual Property (IP) organization, focusing on accurately and timely entering patent prosecution activities into the docketing system. Responsibilities include monitoring communications, creating and maintaining case records, entering deadlines, electronically filing documentation, and generating reports from the docketing system. The position requires a strong understanding of US and international patent law and procedure, advanced proficiency with docketing systems and patent office databases, and excellent attention to detail.

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 Senior Specialist in Metrology and Validation within the Pharmaceutical Analysis & Digital Technologies department at Merck. The primary focus is on onboarding, qualifying, validating, and maintaining analytical equipment and instrumentation in a GMP environment, ensuring compliance with regulations like 21CFR11. Responsibilities include leading computer system validation, documentation, audit support, and mentoring junior specialists. The role requires a Bachelor's degree in a relevant field with 5+ years of experience, strong problem-solving, and communication skills.

Director, Global Communications, Oncology role at Merck, managing communications for the company's oncology portfolio and pipeline. Responsibilities include leading communications for in-line products and pipeline assets, emphasizing milestone communications, developing omni-channel strategies, advising regions, liaising with external groups, managing agencies and budgets, and supervising a direct report. Requires 8+ years of experience in communications/PR in the pharmaceutical industry.