Merck

This role supports safety reporting in clinical trials for investigational drug development programs. Responsibilities include intake of safety event information, managing and creating individual case safety reports, generating safety queries, and ensuring timely submission of events. The role requires collaboration with cross-functional teams and adherence to GCP and ICH regulations.

Senior Engineering Specialist at Merck focused on supporting packaging operations. Responsibilities include analyzing operating performance, managing data in SAP, applying problem-solving techniques, strengthening compliance, and investigating deviations. The role involves leading improvement initiatives, implementing new technology, managing projects, authoring deviations and CAPAs, and optimizing standardized work. Requires a Bachelor's in Engineering and 5 years of industrial experience, with preferred skills in Lean/Six Sigma, SAP, and data analysis software.

This role supports packaging operations by analyzing performance, managing data in SAP, applying problem-solving techniques, strengthening compliance, and investigating deviations. It involves leading improvement initiatives, implementing new technology, managing small projects, authoring deviations and CAPAs, and optimizing standardized work. The role requires a BS in Engineering, 2+ years of industrial experience, strong analytical, communication, and project management skills, and technical writing experience. Preferred skills include cGMPs, Lean/Six Sigma, SAP, and data analysis software.

This role at Merck focuses on Health Economics and Outcomes Research (HEOR) within the Market Access department. The primary responsibilities involve scientific coordination and study leadership for medico-economic and epidemiological data generation, particularly in oncology. The role aims to support product recognition and market access by ensuring scientific rigor and valorization of projects for health authorities and internal stakeholders. It requires strong leadership, strategic vision, analytical rigor, and collaboration skills, with a focus on economic modeling and epidemiological studies.

Seeking an Engineering Senior Specialist to design, engineer, and operate enterprise-scale XDR and SIEM platforms across Microsoft and Google security ecosystems. This role focuses on security platform engineering, detection engineering, and operational resilience to improve threat detection, response effectiveness, data fidelity, and platform reliability. Requires deep hands-on engineering expertise, an operations-first mindset, and collaboration with SOC, cloud, identity, and infrastructure teams.

Finance Clinical Operations Manager at Merck, responsible for clinical trial performance and compliance in the UK, focusing on budget and finance aspects. The role involves managing budgets, negotiating contracts, and ensuring adherence to regulations.

This is a junior accounting role focused on preparing and analyzing monthly and annual accounting closings in USGAAP and PCG standards. The role also involves being a point of contact for accounting questions, proposing improvements to internal procedures, and participating in the digitalization of work methods. Experience in a public accounting firm or international company is recommended, and an aptitude for data and digital tools is a plus.

Specialist Engineer (m/f/d) for Merck's pharmaceutical/chemical production site in Vienna, focusing on technical support for investment, renovation, and optimization projects. Responsibilities include requirements gathering, concept development, project team participation, specification creation, tender preparation, and supporting installation, commissioning, qualification, and validation activities. The role also involves assisting with deviations, CAPAs, change requests, and ensuring HSE compliance throughout project lifecycles. Requires a technical or higher education, business administration background, and at least 3 years of relevant experience.

Associate Director, Marketing Excellence role at Merck, focusing on refining brand marketing strategy, enhancing market insights, strengthening data-driven decisions, and improving customer engagement and execution excellence within the pharmaceutical industry. Responsibilities include shaping marketing frameworks, capability building, and piloting new approaches. Requires 8+ years of experience in pharmaceutical strategic marketing or commercial leadership.

Merck is seeking a Bioprocess Technician for their Tissue Culture department in Boxmeer. The role involves executing and monitoring cell and virus culture processes, preparing media, and performing various downstream processing steps in a GMP-compliant environment. The position requires a technical background, preferably with experience in GMP or aseptic processes, and fluency in Dutch.

Senior Pharmacovigilance Specialist responsible for country PV activities including intake, agreement management, due diligence, audits, inspections, compliance review, SOP management, training, and safety issue communication. May serve as backup local Qualified Person for PV.

This role is for a Manufacturing Engineering Lead at Merck, supporting specialty dosage forms and oral solid dosage (OSD) GMP development activities. The lead will be responsible for technical decisions during their shift, ensuring safety, quality, and equipment performance. Key responsibilities include evaluating production status, troubleshooting equipment, authoring GMP documentation, and leading improvement initiatives. The role requires a Bachelor's degree in Engineering or Science with at least 5 years of GMP manufacturing experience.

Senior IT Solution Specialist role focused on IT infrastructure management, project/service management, and bridging the gap between IT and business in a manufacturing/shopfloor environment. The role involves developing and implementing IT solutions, managing IT initiatives, and driving digital transformation. Experience in life sciences or manufacturing is preferred. The role emphasizes technical expertise in IT infrastructure and systems management, project/service management (ITIL), and strong hands-on and communication skills.

Product Analyst role within Merck's R&D division, supporting Patient Safety and Quality & Compliance. The role focuses on translating business needs into IT requirements, collaborating with stakeholders, leading testing, and ensuring product outcomes. It involves understanding business strategy, IT architecture, and delivering IT solutions. The position requires strong analytical skills, experience in IT business analysis, and familiarity with software development lifecycles. Experience in the pharmaceutical industry and with regulatory compliance is a plus.

Senior Maintenance Engineer role focused on executing corrective and preventative maintenance for process equipment in a pharmaceutical manufacturing setting. Responsibilities include technical expertise, deviation investigations, root cause analysis, implementing technical solutions for equipment uptime, and ensuring compliance with safety and quality standards. The role also involves equipment project management and reliability improvement using Lean Six Sigma tools.

Associate Specialist, Engineering Intern role at Merck in Singapore, focusing on assisting the maintenance team with planned work, inventory management, quality system improvements, and vendor management within a cGMP pharmaceutical manufacturing environment. This internship offers exposure to inventory management, quality systems, cGMP, vendor engagement, and preventive maintenance processes.

Merck is seeking a Regulatory Liaison to manage regional regulatory strategy for products, ensuring compliance with health authority requirements for registration and lifecycle maintenance. This role involves serving as a key point of contact, contributing to development strategies, and managing responses to health authority questions.

Associate Director, Site Sterility Lead at Merck in Dundalk, Ireland, focusing on driving excellence in sterile manufacturing, aseptic standards, contamination control, and regulatory compliance (EU GMP Annex 1, cGMP). Responsibilities include leading training programs, serving as a Subject Matter Expert for sterility assurance, managing the Environmental Monitoring Program, performing quality risk assessments, and ensuring inspection readiness.

Strategic Account Manager for Merck's Companion Animal Health AU, responsible for developing and executing strategic plans to maximize value and growth of key accounts (Retailers and Onliners). The role involves understanding account needs, market trends, and company capabilities to create tailored solutions, drive brand activity and sales, and achieve sales targets. Requires strong strategic thinking, commercial acumen, relationship management, and collaboration with internal teams.

Associate Director Medical Affairs for Vaccines & Infectious disease responsible for developing and executing the Country Medical Affairs Plan, engaging with scientific leaders, and collaborating cross-functionally. The role involves providing scientific information, managing budgets for medical education programs, and supporting clinical development.

Co-op position supporting manufacturing and reliability engineering in vaccine manufacturing facilities, focusing on equipment troubleshooting, maintenance programs, and utility systems. Requires pursuing an engineering degree and strong communication skills.

Co-op position in Vaccine Manufacturing at Merck, supporting operational activities, deviation investigations, and process improvement projects using Lean Six Sigma tools. Requires pursuit of an engineering or science degree.

Medical Manager role at Merck focused on overseeing the Country Medical Affairs Plan, translating global medical goals into local tactics, and engaging with scientific leaders and stakeholders. The role involves budget management, cross-functional collaboration, and providing scientific information and training. Requires experience with pharmaceutical industry guidelines and regulatory frameworks.

Merck is seeking a Bioprocess Technician to contribute to the production of animal vaccines. The role involves various stages of the production process, including preparing and filling vaccines, freezing and storing products, and operating equipment under strict GMP and safety guidelines. The position requires a relevant vocational or higher education and offers comprehensive internal training.

Clinical Research Associate responsible for managing and monitoring assigned clinical trial sites to ensure compliance with ICH/GCP, local regulations, and internal policies. This role involves site management, study start-up, maintenance, close-out, quality assurance, and territory development, acting as a primary point of contact for investigators and site staff.

This role provides after-sales technical support for livestock intelligence solutions, including monitoring, milking systems, and RFID readers. Responsibilities include fault finding, troubleshooting hardware, software, and connectivity, delivering proactive support, conducting site surveys, coordinating installations, providing customer training, and managing post-sales technical issues. The ideal candidate has experience in technical fault finding, farm-based equipment support, and strong customer-facing skills.

This role supports the Trade Affairs & Patient Supply department at Merck, focusing on the procurement, logistics, sales, customer service, negotiations, and distribution of medications and vaccines. The intern/working student will assist with projects, customer-oriented technologies, data management, and event planning within the pharmaceutical industry.

Administrative Executive role at Merck's Singapore Tech Center, focusing on providing comprehensive administrative and operational support to leadership and teams. Responsibilities include calendar management, event and travel coordination, office support, business continuity, and stakeholder management. Requires 5+ years of experience, proficiency in SAP Concur and Microsoft Office Suite, and strong organizational skills.

This role focuses on translating global medical goals into local strategies and tactics to improve patient outcomes in China within a defined therapeutic area, likely oncology. Responsibilities include building trust with the scientific community, providing medical input to brand strategy and lifecycle management, supporting clinical trials, generating study concepts from local data, and collaborating with internal and external stakeholders. The role also involves reviewing promotional materials and ensuring compliance with local laws and company regulations.

Merck is seeking a Medical Science Liaison (MSL) for their General & Specialty Medicine division, focusing on the Immunology therapeutic area in Tokyo, Japan. The role involves scientific discussions with medical/scientific leaders, gathering insights, and contributing to healthcare improvements. It requires a strong scientific background, communication skills, and strategic thinking. The position is open to individuals with a medical, pharmacy, or life sciences background, and experience in pharmaceutical medical affairs or academia is preferred.

Area Manager for Vaccine Alliance & Customer Engagement in Henan, China. Responsibilities include dealer management, customer engagement, ecosystem building, and ensuring compliance within the vaccine market. Requires 5+ years of experience in the pharmaceutical or sales management, preferably in vaccines.

Area Manager for Vaccine sales and customer engagement in China, focusing on dealer management, customer relationship building, ecosystem development, and ensuring compliance within the pharmaceutical industry.

Senior Principal Scientist (Senior Director) in Clinical Research for Oncology Asset therapeutic area at Merck. Responsibilities include planning and directing clinical research activities for new medicines, from early to late clinical development. This involves study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. The role also includes evaluating pre-clinical and translational work, developing clinical development strategies, and providing expert scientific opinion.

This role is for a Sr. Global Director of Medical Affairs in Rheumatology at Merck. The position involves supporting the execution of scientific and medical affairs plans, collaborating with R&D, Value & Outcomes Research, Policy, Commercial, and Market Access teams. The director will engage with scientific leaders, organize expert input events, and support local data generation studies. The role requires an MD, PhD, or PharmD with expertise in rheumatology and experience in global medical affairs or clinical development.

Operates and maintains equipment and machinery for a cogeneration power plant, including natural gas turbines, steam distribution, water treatment, and electrical grid systems. Responsibilities include monitoring systems, maintaining logs, performing routine maintenance, troubleshooting, and ensuring efficient operation within environmental emissions limits.

Specialist role focused on metrology and validation of analytical equipment within a GMP environment for pharmaceutical research laboratories. Responsibilities include onboarding, qualification, maintenance, and computer system validation of laboratory equipment, as well as supporting audits and managing documentation.

The Analytical Instrument Validation Specialist will work as part of the integrated Validation and Compliance team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and/or supports the validation of novel computerized analytical instrumentation within the GMP environment for multiple sites.

Merck is seeking a Senior Specialist - Continuous Improvement Lead to drive continuous improvements and operational excellence at their Friesoythe site. The role involves analyzing and redesigning production processes, moderating improvement projects, implementing KPIs, fostering a Lean culture through training and coaching, and managing change processes. The ideal candidate has a degree in a relevant field, at least 5 years of production experience, strong project management skills, and deep expertise in Lean Management methodologies.

This role is responsible for driving business growth through product portfolio strategy, identifying strategic opportunities, and fostering cross-functional collaboration within the Pharma and Specialty Business Unit (PSBU). Key duties include performing data analysis, developing performance monitoring dashboards, supporting go-to-market strategies, building financial models for forecasts, and collaborating with stakeholders to monitor performance and streamline processes.

This role focuses on the implementation, configuration, and lifecycle management of analytical instruments and systems within a digital validation system in a pharmaceutical setting. It involves leading technical implementation, collaborating with stakeholders to define requirements, executing SDLC deliverables, and ensuring compliance with data integrity regulations. The role supports the digitization and integration of laboratory instruments to create efficient and connected labs.

This role focuses on developing and maintaining solutions using SAP Build tools (Work Zone, Apps, Process Automation) integrated with SAP BTP and S/4HANA. It requires a blend of low-code/no-code and pro-code skills in SAP Fiori/UI5, CAP, Node.js, ABAP, CDS, and OData, aiming to improve usability and modernize business processes.

Senior DevOps Engineer role focused on enhancing infrastructure and CI/CD processes using technologies like Terraform, Crossplane, Argo CD, Docker, Kubernetes, AWS, and Azure. Responsibilities include collaborating with teams, managing cloud infrastructure, implementing containerization, performing POCs, and optimizing costs and security.

The Regulatory Affairs Specialist role at Merck is responsible for ensuring timely preparation, submission, and follow-up of new Marketing Authorization applications and maintenance of existing ones for assigned products. This includes managing translations, artwork, and staying updated on EU and local regulations. The role involves close cooperation with internal departments and external regulatory agencies to ensure compliance and facilitate new medical advancements.

Maintenance Technician role at Merck's Animal Health facility in Boxmeer, NLD. Responsible for maintaining high-tech installations, diagnosing and resolving technical failures, and executing preventive maintenance plans for machines in a sterile, cleanroom GMP-compliant environment. Involves planning, coordinating with internal/external parties, and providing technical advice. Requires participation in on-call duty. Focus on ensuring machine availability and reliability.

Operator Mediabereiding (Media Preparation Operator) at Merck's Animal Health division in Boxmeer, Netherlands. Responsible for preparing media and buffers, transferring products, and ensuring quality, hygiene, and safety in a pharmaceutical production environment. Requires MBO level 3 education and experience in biological processes and pharmaceutical production.

Merck is seeking a Pharmaceutical Specialist in Haarlem to ensure the quality of pharmaceutical products by overseeing GMP compliance, handling deviations, change control, and documentation. The role involves advising on process changes, evaluating external guidelines, approving documentation, leading quality issue investigations, and contributing to quality improvements and strategy.

Merck is seeking a Pharmaceutical Specialist in Haarlem, NLD, to ensure the quality of pharmaceutical products. This role involves managing GMP compliance, handling complaints, deviations, change control, documentation, and supporting audits. The specialist will advise on process changes, evaluate external guidelines, approve deviations, lead investigations for quality issues, and contribute to quality improvements and validation strategies. The ideal candidate has an HBO/WO/MSc in a pharmaceutical, process-technical, or life sciences background with 2-3 years of relevant experience in quality or production, and strong knowledge of GMP, deviation investigations, and SAP.