Merck

Merck is seeking a Senior Specialist, QE Engineer in Hyderabad to lead a Quality Engineering team, build high-throughput testing capabilities, and mentor test engineers. The role involves defining test strategies, building automation scripts (Robot Framework, TOSCA, Load Runner), integrating tests into CI/CD pipelines on AWS, and ensuring adherence to regulatory requirements (GLP/GCP). The candidate will also manage test engineers, oversee testing artifacts, and collaborate with cross-functional teams.

This role is for a Senior Specialist in SAP Data Engineering at Merck, a global healthcare company. The primary focus is on the design, development, and global rollout of SAP BI solutions, specifically involving SAP BW/HANA. Responsibilities include requirements gathering, technical design, development, testing coordination, and post-go-live support, adhering to SDLC standards. The role also involves contributing to ECC to S/4HANA migration remediation activities within a diverse, globally distributed team. Experience with SAP BW, HANA, data modeling, SQL, and cross-functional collaboration is required, with a strong emphasis on operating in a regulated pharma environment.

This role focuses on technology risk management and cybersecurity within the Animal Health division of a global healthcare company. The Senior Specialist will partner with business and technology teams to identify, assess, and advise on information security and compliance risks, ensuring that security and privacy considerations are integrated into projects and operations. The role involves translating technical risks into business context, supporting risk governance, and contributing to the adoption of security standards, with an awareness of emerging technologies like AI.

Maintenance Technician role focused on performing and documenting routine maintenance, resolving equipment breakdowns, ensuring GMP and legislative compliance, and supporting production schedules within an Engineering Centre of Excellence at Merck.

This role is for a Stamping Process Worker at Merck in New Zealand. The primary responsibility is to operate stamping machines, ensure products meet quality standards, and remove faulty products. The role involves inspecting stamping on tags, adjusting processes, completing production records, maintaining a clean workspace, reporting machine malfunctions, and adhering to safety precautions. Required skills include customer focus, communication, problem-solving, attention to detail, and teamwork. Preferred skills are not specified, but the role is in an animal health organization.

Senior Data Governance Analyst role at Merck, focusing on ensuring data integrity, quality, security, and compliance for commercial and medical affairs data domains. Responsibilities include requirement analysis, stakeholder communication, Collibra DGC environment setup and maintenance, metadata management, and documentation.

This role focuses on engineering and developing Master Data Management (MDM) and Reference Data Management (RDM) solutions, primarily using Informatica IDMC. The engineer will be responsible for designing, developing, and maintaining these products, integrating them with various enterprise systems, and ensuring data quality and governance. The role requires strong data engineering skills and experience within the life sciences domain.

Manager for Quality COE in Lab Support SDLC at Merck, focusing on leading a team of quality specialists for laboratory system qualification, lifecycle management, and ensuring compliance with pharmaceutical manufacturing standards.

Seeking a Senior Engineer/Scientist to lead the development and implementation of specialized testing methodologies for combination products (e.g., prefilled syringes, auto-injectors, infusers). The role involves test method development/validation, design verification, technical feasibility evaluation, establishing design inputs/outputs, and driving technology transfers. Expertise in medical device and combination product design controls, risk management, and material characterization is required.

This role focuses on designing, implementing, and maintaining the organization's virtualized infrastructure (VMware) and Windows server environments. Key responsibilities include managing virtual machines, Active Directory, Group Policy, and automating tasks using PowerShell. The role requires expertise in VMware and Windows administration to ensure high availability, performance, and security of IT services.

This role focuses on designing, implementing, and maintaining the organization's virtualized infrastructure (VMware) and Windows server environments. Key responsibilities include managing virtual machines, Active Directory, Group Policy, and automating tasks using PowerShell. The role requires expertise in VMware and Windows administration to ensure high availability, performance, and security of IT services.

This role supports pharmacovigilance activities within the pharmaceutical industry, focusing on ensuring adherence to regulations, managing adverse event cases, and supporting PV processes. It involves collaboration with internal and external parties, local audits, and maintaining PV procedures.

This role is for an Electrical & Instrumentation Technician in a biopharmaceutical manufacturing setting, participating in a two-year training program to develop skills in the industry. Responsibilities include supporting maintenance, inventory management, quality system improvements, vendor coordination, and basic diagnostic of equipment failure.

This role is for a Specialist in Manufacturing Automation Engineer at Merck, a global healthcare biopharma company. The position, based in Hyderabad or Pune, involves supporting DeltaV automation software change controls for worldwide manufacturing sites. Responsibilities include project management, system upgrades, troubleshooting, documentation, and ensuring compliance with GMPs, CSV, safety, and environmental regulations. The role focuses on implementing automation solutions and supporting digital shop floor technologies within the pharmaceutical manufacturing context.

Senior Archivist role at Merck focused on managing and facilitating archival activities for Nonclinical documents and electronic data, ensuring compliance with Good Laboratory Practices (GLPs) and federal regulations. Responsibilities include indexing, filing, retrieval, electronic archival, supporting regulatory inspections, and coordinating standard archival operations.

This role is for a Senior Software Engineer specializing in Kinaxis Maestro to configure and implement supply chain management software. The responsibilities include translating business requirements into software specifications, leading data integration, managing QA/UAT, and coordinating with product engineering. The role requires experience in Kinaxis Maestro, supply chain planning modules, Python, JavaScript, and Agile methodologies.

Merck is seeking a Specialist Production Support in Krems, Austria, to support biopharmaceutical manufacturing. The role involves process transfer, implementation, optimization, and improvement, as well as handling deviations and change management. The ideal candidate has a science degree, experience in GMP manufacturing, project management, and root cause analysis, with strong quality and safety awareness.

This role is for a Maintenance Lead at Merck's biopharmaceutical facility. The lead will be responsible for managing a maintenance team, ensuring equipment uptime and compliance with GMP standards, and driving continuous improvement projects. The role requires strong people leadership, problem-solving skills, and experience in the pharmaceutical or biotechnology industry.

This role is for an Infrastructure Engineer at Merck, a global healthcare biopharma company. The engineer will be responsible for designing, implementing, managing, and supporting IT infrastructure, including hardware, networking, virtualization, cloud environments, and security systems. The role involves working with VMWare, configuration management tools (Ansible, Terraform), scripting, CI/CD practices, and Git to ensure efficient, reliable, and scalable IT systems. The focus is on supporting the company's digital transformation journey and enabling business outcomes through technology.

Intern role within the Commercial Operations department and Data team at Merck, focusing on the transformation, harmonization, and continuous improvement of data analysis and insights creation using data platforms to deliver actionable business insights. Requires skills in data analysis, Excel, and preferably visualization tools like Power BI.

The Regional Dossier Publisher (RDP) is responsible for publishing key regulatory submissions in the EU+EEMEA region, supporting the publishing work of the regional team. This role requires knowledge of regulatory procedures and dossier requirements, and involves supporting country RA teams with local publishing and submission transmission needs. The RDP will also assist in the development of tools and procedures for submission publishing.

This role is for a ServiceNow Developer responsible for designing, coding, testing, and implementing solutions within the ServiceNow platform to meet ITSM, Service Portal, and Virtual Agent requirements. The developer will collaborate with cross-functional teams, integrate ServiceNow with other systems, and support reporting and analytics.

Technical Project Manager responsible for end-to-end project management and delivery of technical deliverables for assigned clinical trials within a specific drug/vaccine program. This includes developing and managing technical project plans from design through production deployment and change management, collaborating with functional areas to secure resources, and engaging with cross-functional stakeholders. The role also involves serving as a point of contact for in-life maintenance, managing change requests, customer expectations, facilitating decision-making, and performing risk management.

Animal Technician role at Merck focused on daily animal care, cleaning, and maintenance of animal facilities. Responsibilities include performing biotechnological procedures with a focus on animal welfare, administering anesthesia, and conducting animal studies. The role requires adherence to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines, accurate data recording, and observation of animal health. Requires an MBO-4 diploma and relevant certifications in animal experimentation. Experience with quality systems like GLP/GMP is preferred.

Associate Director, Engineering role at Merck focused on planning, design, and implementation of capital projects within pharmaceutical manufacturing. This role involves collaboration with various teams, equipment selection, vendor management, and overseeing project execution from start to finish. It requires a strong understanding of GMP manufacturing and project leadership.

Associate Director, Engineering role at Merck focused on providing technical support to vaccine manufacturing operations within a cGMP environment. Responsibilities include leading a team, coordinating responses to process upsets, prioritizing projects, and supporting regulatory audits. Requires a strong background in biological and/or vaccines industries with experience in manufacturing and problem-solving.

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.

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.

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 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.

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 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 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.

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.

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.

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.

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.