Merck

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.

This role is for a Senior Specialist, Software Engineer at Merck, focusing on configuring and implementing Kinaxis Maestro for supply chain management. The responsibilities include translating business requirements into software specifications, leading data integration, managing QA/UAT, and coordinating with product teams. The role requires expertise in Kinaxis Maestro, supply chain planning modules, and proficiency in Python and JavaScript for data integration.

The QA Supervisor oversees quality assurance for veterinary pharmaceuticals, ensuring products meet standards and regulations. Responsibilities include team leadership, regulatory compliance (WHO-GMP), QMS improvement, documentation, audit readiness, training, risk management, supplier oversight, customer complaint handling, new product launches, and problem-solving.

This role focuses on implementing data analysis practices to support business objectives in sales and marketing, improve efficiency, and foster a data-driven culture through intuitive visualizations. The specialist will also manage data analysis platforms, ensuring quality and performance standards.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Senior Site Reliability Engineer responsible for the reliability, scalability, and security of critical platforms and applications in a global healthcare biopharma technology team. The role involves hands-on engineering, driving modernization, shaping operational best practices, mentoring engineers, and collaborating across products and regions to deliver resilient, high-performing systems.

The role focuses on industrial automation and robotics maintenance, repair, and modernization within a manufacturing environment. Responsibilities include troubleshooting, analyzing failures, upgrading machine controls, managing technical documentation, and training technicians. It requires experience with PLC and HMI programming, electrical systems, and basic robot operation.

Seeking a Senior Glass and Critical Component Technical Expert for pharmaceutical and combination product engineering projects. Responsibilities include design, development, manufacturing, qualification, supplier oversight, and lifecycle support of glass primary containers (syringes, vials, cartridges). Requires materials science, failure analysis, process control, and regulatory knowledge to ensure component performance, supply robustness, and patient safety. Role involves leading technical investigations, defining specifications, executing qualification packages, developing process control strategies, managing suppliers, and collaborating cross-functionally with quality, regulatory, and device engineering teams. Mentorship of junior engineers is also expected.

Software Engineer role in Finance IT at Merck, focusing on designing, developing, and supporting Treasury applications and integrations with ERP and external financial institutions in a global, regulated environment. Requires experience with TMS, complex integrations, and modern software engineering practices.

Warehouse worker responsible for receiving, dispatching, loading, unloading, and inventory management of materials and products. Requires basic math and computer skills, attention to detail, and organizational abilities. Forklift operation is a key part of the role, with training offered.

This role supports the implementation and enhancement of Global Regulatory Affairs, Compliance and Safety (GRACS) Digital Strategy projects and systems within the healthcare industry. It involves managing content for regulatory submissions, submission planning, health registration, and regulatory information management systems. The role partners with various teams to ensure successful regional implementation and continuous improvement of systems and processes, including evaluating regional data for quality issues and exploring automation opportunities.

Supervisor de Produccion (Production Supervisor) for an industrial plant manufacturing plastic caravans for livestock identification. The role focuses on managing the production sector end-to-end, with a strong emphasis on people leadership, safety, quality, and continuous improvement using methodologies like LEAN/TPM and 5S. Responsibilities include team management, performance coaching, talent development, operational management, and reporting.

Director of Drug Substance Commercialisation & Development at Merck, responsible for the strategic and technical leadership of introducing, developing, and commercially manufacturing active pharmaceutical ingredients (APIs). This role involves end-to-end accountability for process development, scale-up, validation, and lifecycle management, ensuring safe, compliant, and robust supply while driving continuous improvement.

Senior Specialist role in Quality Control at Merck, focusing on laboratory system lifecycle management, compliance, and quality improvement initiatives within a GMP-regulated healthcare environment.

This role involves operating and monitoring chemical production processes, ensuring adherence to quality and safety standards, completing batch documentation, and meeting production targets. Responsibilities include process monitoring, sampling, material handling, and potentially leading a team of technicians. The role requires a diploma or equivalent experience in engineering or science, with a strong awareness of cGMP and SHE regulations.

Mechanical Process Engineer role at Merck in New Zealand, focusing on supporting the Engineering Centre of Excellence to meet site KPIs by delivering projects, leading problem-solving, and performing advanced process and technical activities. The role involves ensuring compliant product supply for the Animal Health site, applying process and mechanical engineering expertise, managing projects, and driving equipment and system improvements.

This role is for a Utilities and HVAC Engineer at Merck in Singapore. The engineer will oversee the IFM Utilities and HVAC team, ensuring systems are functioning correctly. Responsibilities include supporting cost improvement projects, monitoring and analyzing utility parameters for early failure detection, and ensuring environmental conditions in warehouses and microlabs are maintained. The role also involves preparing annual review reports, supporting QRA reviews for HVAC, water, and compressed gas systems, and assisting with project impact assessments for utilities and HVAC systems. A Bachelor's degree in mechanical or electrical engineering and 2-3 years of operational experience with utilities and HVAC systems are required, along with minor project management skills.

This role is for a SAP SCM Variant Configuration Consultant at Merck, focusing on supporting business processes within the Animal Health sector. The consultant will partner with business stakeholders, manage projects, and ensure the integrity of the global template in the ERP system. Key responsibilities include approving changes, building relationships with business owners, and supporting the second-line support team. Requirements include in-depth knowledge of SAP SCM (SD/PP/MM) solutions, extensive experience with SAP customizing, and specific expertise in SAP Variant Configuration.

Associate Director role focused on end-to-end operational readiness planning and execution for a new Antibody Drug Conjugate (ADC) manufacturing facility. The role integrates cross-functional workstreams, drives schedule acceleration, ensures governance, and prepares the site for GMP manufacturing, PPQ, and facility approval through SOPs, training, tech transfer, and risk controls. It emphasizes operational excellence from day one in a regulated environment.

This role is for a Sr. Specialist in SAP Master Data within Merck's Vaccines and Advanced Biotechnologies Process R&D. The position supports pilot-scale GMP manufacture, focusing on creating, designing, and sustaining standardized business processes, master data governance, and system lifecycle management. The role involves collaboration with various teams, ensuring alignment with global processes and regulatory requirements, and driving continuous improvement in master data accuracy and compliance. The position will temporarily be based in West Point, PA, before relocating to Rahway, NJ.

Associate Principal Scientist, Microbiology AR&D role at Merck, supporting second shift operations in Rahway, NJ. The position focuses on leading and executing microbiology testing within a GMP laboratory, including finished product testing, utilities monitoring, and environmental monitoring. Key responsibilities involve ensuring compliance, managing contamination control strategies, supporting sterile operations, and leading investigations. Requires extensive experience in pharmaceutical microbiology, GMP practices, and environmental monitoring programs.

Operations Technician at Merck's Animal Health facility in Worthington, Minnesota, focusing on the preparation of intermediate components for vaccine manufacturing, including media solutions, seed stocks, and bacterial antigens, as well as downstream processing. The role involves operating fermentation vessels, working in a cleanroom environment, and adhering to cGMP guidelines.

Manager, Engineering role at Merck's manufacturing facility in Elkton, Virginia. Focuses on coordinating maintenance activities, managing a union workforce, and ensuring operational efficiency and compliance with cGMP, safety, and environmental regulations. Responsibilities include equipment startup support, process validation, staff training, safety audits, and implementing continuous improvement initiatives. Requires experience in cGMP, manufacturing, or maintenance environments, with strong leadership, communication, and problem-solving skills. Experience in reliability engineering, predictive maintenance, and process safety management is required.

The Senior Platform Engineer will define standards and architecture patterns for data quality and observability platforms, manage Terraform deployments, implement environment provisioning, and develop CI/CD pipelines. This role requires strong cloud knowledge (AWS), DevOps tools, Python, SQL, and experience with product development principles.

Senior Specialist, Drug/Device Combo Products Engineer at Merck, focusing on the development, manufacturing, and assembly of medical devices and combination products. Responsibilities include hands-on factory floor work, supplier collaboration, process interrogation, and supporting quality control strategies. Requires expertise in vision inspection systems, PLC programming, and mechanical troubleshooting within a regulated industry.

This role focuses on implementing and optimizing SAP Ariba Supply Chain Collaboration (SCC) solutions, including configuration, customization, and vendor onboarding. It requires expertise in SAP Ariba SCC, Cloud Integration Gateway (CIG), and SAP Materials Management (Procure to Pay) to enhance supply chain processes and collaboration.

This role is for a General Accounting Specialist at Merck, focusing on financial accounting and reporting for multiple entities. Responsibilities include general ledger accounting, managing fixed assets and project accounting, overseeing inventory accounting, and supporting audits. The role requires a degree in accounting, auditing, or finance with at least 3 years of experience and knowledge of US GAAP and Dutch GAAP. Experience with Analytic Data and Prescriptive analytics is a preference.