This role is for a Pharmaceutical Information Manager at Merck, responsible for promoting company products within a designated region, building relationships with healthcare institutions, and achieving sales and market share targets. The role involves market analysis, sales strategy development, and ensuring product knowledge.

This role is for a Pharmaceutical Information Manager at Merck, responsible for promoting company products within a designated region, building relationships with healthcare institutions, achieving sales targets, and managing regional market share and growth. The position involves detailed planning, execution of sales strategies, market analysis, and maintaining product knowledge.

This role is for a Sr. Innovation & Engagement Specialist at Merck in Chengdu, China. The primary responsibilities involve promoting company products within a designated region, building relationships with healthcare institutions, achieving sales targets, and managing regional market share and growth. It requires a Bachelor's degree, 2-3 years of experience as a hospital pharmaceutical representative, and skills in product knowledge, promotion techniques, and regional management. The role is focused on sales and market development, not AI/ML development.

Merck is seeking an Executive Director to lead clinical research activities for new or marketed medicines in Hematology, overseeing the entire late-stage clinical development cycle from Phase 2 to Phase 5. This role involves strategic planning, protocol authoring, execution, monitoring, analysis, regulatory reporting, and publication. The Executive Director will lead cross-functional product development teams, provide scientific leadership, and interact with key scientific leaders and regulatory agencies. Responsibilities include evaluating pre-clinical work, developing clinical strategies, managing clinical trials, analyzing findings, supporting business development, and managing clinical directors. The role requires a strong scientific fund of knowledge, awareness of scientific developments, and collaboration with investigators and external researchers. A minimum of 3 years of clinical medicine experience and 5 years of industry drug development experience are required, along with experience in authoring regulatory documents and a demonstrated record of scientific scholarship.

Principal Scientist role focused on sterilization science and sterility assurance for parenteral dosage forms (injections, implants, ophthalmic, inhaled products) from preclinical to commercialization within a cGMP-regulated environment. Responsibilities include defining, evaluating, and implementing sterilization strategies, leading cycle development and validation, and providing technical leadership on cross-functional teams. Requires expertise in sterile drug product development, sterilization technologies, and regulatory expectations.

Senior Scientist role focused on chromatographic isolation of pharmaceutical API and impurities, from analytical to semi-prep and prep scale, for various modalities including small molecules, peptides, and conjugates. The role involves method development, partnering with chemists, and delivering high purity materials to support drug development.

Medical Manager role at Merck focused on developing and executing the Country Medical Affairs Plan, engaging with scientific leaders, and collaborating cross-functionally to improve patient outcomes. Requires MD/PharmD and clinical/research experience, with a strong emphasis on pharmaceutical industry guidelines and stakeholder engagement.

The Senior Scientist, Cell Based Sciences role at Merck focuses on the design, execution, and interpretation of cell-based assays and immunoassays for vaccine development. This involves method development, optimization, and transfer to support drug substance and product release, stability studies, and characterization. The role requires expertise in cellular biology, virology, and immunology, with a strong emphasis on assay development and understanding vaccine mechanisms of action. Experience in a GxP regulated environment and with cell line engineering is desirable.

This role is for a Sr. Specialist in Field Enablement Planning & Execution within Merck's US Market. The primary focus is on project management, program orchestration, and day-to-day execution of cross-functional initiatives to optimize the customer-facing sales organization. Responsibilities include managing timelines, dependencies, risks, and ensuring synchronized delivery of projects. The role involves collaboration with various departments including Sales, Marketing, HR, Compliance, Legal, and Data Science functions, but does not involve direct AI/ML development.

Internship role focused on cellular pharmacology and assay development within a biopharmaceutical research setting. The role involves conducting cell-based assays, engineering cell models, and analyzing experimental data to support the discovery of new therapeutics.

This is a co-op position for students in an Engineering program at Merck, focusing on Global Workplace and Enterprise Services. The role involves assisting with facility services, operational data trending, creating dashboards, supporting safety programs, and developing digital tools for automation and process simplification. It is a project-based role with a deliverable in mind, aimed at providing hands-on experience in various support functions within the company.

Associate Director, Engineering role at Merck focused on leading end-to-end program management for clinical manufacturing campaigns, specifically campaign preparation and closeout execution. The role involves driving cross-functional alignment, ensuring timely drug substance release, overseeing material transfer, and mitigating risks. Key responsibilities include partnering with process leadership for operational excellence, managing campaign timelines, developing training strategies for rapid ramp-up of new engineers, and overseeing process-related quality documentation and changes. Requires a BS/MS in Engineering or Biological Sciences with 7+ years of relevant pharmaceutical/biopharmaceutical industry experience, including technical knowledge of fermentation, cell culture, purification processes, GMP environments, and quality systems.

Associate Director, Engineering for Small Molecule packaging development at Merck. This role leads packaging strategies, designs, processes, and control strategies for new oral solid dosage and parenteral products, ensuring robustness, efficiency, and compliance with global regulatory standards and sustainability goals. Requires strong technical, problem-solving, and project management skills within the pharmaceutical development continuum.

The Marketing Operations Specialist is responsible for the flawless execution of marketing initiatives, ensuring speed, consistency, and alignment with commercial objectives. This role acts as an operational/analytical hub, connecting strategy, field execution, and results tracking, with a clear focus on adoption, conversion, and brand performance.

Intern position in Demand Planning within the Supply Chain Management team at Merck in Quito, Ecuador. Responsibilities include supporting project tracking, administrative tasks, logistics operations, innovation projects, and updating demand reports and KPIs. Requires a degree in Business Administration or Economics, intermediate English, and Excel skills.

This role is a Senior Territory Representative for Merck's Animal Health division, focusing on selling Companion Animal products to veterinary clinics, shelters, and corporate accounts. The representative will identify customer needs, develop sales strategies, manage accounts, analyze sales results, and collaborate with internal teams and distribution partners to drive sales growth. The role requires strong sales, communication, and interpersonal skills, with a focus on understanding customer needs and offering relevant solutions within the Animal Health industry.

Senior Scientist, Analytical R&D role at Merck focused on externalizing analytical deliverables for large molecule development programs. Responsibilities include building analytical capabilities at external partners, managing projects, overseeing method development and transfer, and ensuring quality documentation. Requires expertise in biologics CMC, GMP, and various analytical methods.

This role supports GMP stability and sample management logistics within a pharmaceutical research division. Responsibilities include sample preparation, labeling, distribution, coordination of shipments, managing stability chambers, maintaining inventory records using digital systems like LIMS, and performing deviations and investigations. The role requires collaboration with internal and external partners and technical supervision of a small team.

This role is for a Senior Utility Engineer at Merck, focusing on supporting manufacturing operations by investigating utility/facility system excursions, implementing improvements, and managing capital projects. The role requires technical expertise in utility systems, problem-solving, and adherence to cGMP requirements within a pharmaceutical manufacturing environment.

This role supports GMP stability and sample management logistics within the Research Laboratories Division, collaborating with analytical scientists and managing analytical samples for stability studies. Responsibilities include receiving, aliquoting, preparing, and shipping samples, maintaining accurate records using digital systems like LIMS, and managing deviations and change controls. The role requires experience in a GMP environment and strong collaboration skills.

The Clinical Research Director is the Clinical Operations lead in a country/cluster, responsible for the execution of all Clinical Trials. This role ensures adherence to local and global policies, manages trial quality, audit responses, and corrective action plans. The Director acts as a single point of contact for clinical trial execution across all phases, supporting strategic development, managing teams, and fostering relationships with investigators and external stakeholders. Key responsibilities include team recruitment and development, budget management, oversight of study execution, and ensuring quality and compliance adherence.

Lead the design and execution of selective data transfers (SDT) into SAP S/4HANA using SAP DMLT solutions. Responsible for data strategy, extraction/mapping/transformation, quality & reconciliation, and coordination with SAP technical teams, business data owners, and project managers to ensure timely, auditable, and business-accepted data cutover.

Managing Director for Animal Health Belgium, responsible for leading, developing, and executing the strategic vision and operational management of the organization, with full accountability for the country P&L and sustainable business performance. This role requires senior leadership experience in animal health or related life sciences, strong commercial acumen, and excellent knowledge of regulatory requirements.

Product Specialist role in the Human Health sector, focusing on pulmonary arterial hypertension. Responsibilities include developing projects to improve patient journeys, conducting physician and hospital meetings, managing product data, and performing data-driven analysis. Requires 4-5 years of industry experience and a valid driver's license.

Merck is seeking an Oncology Associate Brand and Customer Manager to support the launch and promotion of a medication in Egypt. This role involves developing and executing brand and activation plans, managing promotional activities and digital campaigns, engaging with healthcare professionals, supporting sales teams, gathering market insights, ensuring compliance of promotional materials, tracking brand performance, managing budgets, and organizing training sessions.

This role is for a QC Microbiology Analyst at Merck's biologics drug substance facility. The analyst will support routine laboratory operations, including testing, data processing, and microbiology studies, ensuring compliance with cGMP and cGLP standards. Responsibilities include performing various QC Microbiology tests, liaising with stakeholders, adhering to schedules, driving continuous improvement, and supporting audits.

This role focuses on translating business needs into clear, actionable, and technically detailed requirements for data engineering, governance, and analytics teams. The candidate will work with data pipelines, transformations, metadata, access governance, and modern data engineering practices to ensure data products are scalable, well-governed, and fit for purpose.

This role supports the end-to-end meeting process preparation for congress meetings and sponsorships, including creation, vendor management, POs, contracts, compliance review, and payments. It ensures adherence to company policies and financial processes, working with various stakeholders and external agencies. The role involves maintaining documentation, championing process improvements, and resolving operational issues.

Principal Scientist role at Merck focused on the design and development of sterile inhalation dosage forms (DPIs, MDIs, nebulizers, nasal sprays). The role involves leading formulation development, providing technical leadership on program teams, supporting regulatory filings, and mentoring junior scientists. Requires deep expertise in inhalation product development, particle engineering, aerosol characterization, and regulatory expectations.

Senior Principal Scientist role focused on late-stage development of long-acting injectable (LAI) drug products, including depot formulations and extended-release systems. Responsibilities include leading formulation and delivery strategy, providing technical leadership on cross-functional teams, designing studies for release kinetics and stability, supporting process scale-up and validation, and partnering with regulatory and quality teams. Requires deep expertise in parenteral drug product development and LAI formulations.

This role focuses on leading and implementing design controls for drug/device combination products throughout their lifecycle, from concept to commercialization, ensuring compliance with regulatory and company requirements. It involves cross-functional collaboration, risk management, and adherence to medical device and healthcare regulations.

Lead and implement medical device and combination product design controls for new and inline products, from concept to commercialization, supporting regulatory filings, product launch, and post-market surveillance. This role involves working with cross-functional teams, applying product development and design control principles, and ensuring compliance with regulatory requirements.

Lead and implement medical device and combination product design controls, ensuring alignment with global regulatory requirements and driving continuous improvement in design control and risk management processes. This role involves cross-functional collaboration, process optimization using operational excellence tools, and supporting regulatory filings and post-market surveillance.

Director of GMP Site Operations for Pharmaceutical Analytical Sciences, leading a team responsible for GMP analytical activities including cleaning verification, solvent release, and in-process testing for drug substance and drug product. Ensures cGMP compliance, operational excellence, and inspection readiness, while also managing staff development, recruitment, resourcing, and budget.

This role focuses on designing and developing local strategies for Health Economics, Pricing, and Reimbursement Plans, particularly in oncology. It involves creating analytic models and data products to support Market Access, generating insights from data, conducting health economics evaluations, and implementing reimbursement strategies to reduce time to market. The position also manages internal authorizations for value propositions and supports innovative access proposals by providing data insights. Additionally, it includes conducting Non-interventional Local Data Generation studies.

This is a Quality Control Specialist role focused on laboratory analysis and compliance within the pharmaceutical industry. The responsibilities include ensuring adherence to good laboratory practices, managing equipment, maintaining data integrity, and participating in audits. The role requires a degree in a relevant scientific field and at least one year of experience in analyzing raw materials and finished products.

Clinical Research Associate (CRA) responsible for ensuring performance and compliance of assigned clinical research sites. This role involves site management, monitoring, data integrity checks, regulatory documentation, and communication with investigators and internal/external stakeholders, all while adhering to ICH/GCP standards and local regulations.

This role is a Customer Service Representative at Merck, focusing on customer satisfaction, sales, and end-to-end order management. It requires strong communication, problem-solving, and data interpretation skills within a regulated environment.

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.

Scientist role in Pharmaceutical Analytical Sciences at Merck, focusing on laboratory-based analytical characterization and statistical data analysis for drug development. Responsibilities include supporting scientific studies, developing analytical methods, troubleshooting, documenting experiments, and authoring technical reports for regulatory submissions. Requires a Bachelor's or Master's degree in a relevant field with a minimum of 0-3 years of experience. Collaboration and communication skills are essential.

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.

Senior Specialist role in Quality Risk Management & Auditing within a GMP environment at a biologics R&D facility. Focuses on leading site governance for QRM and Auditing, ensuring inspection readiness, building quality culture through training, driving robust QRM processes, supporting audits, and enhancing Quality Systems. Requires at least 5 years of experience in a GMP pharma/biotech QA, QRM, or auditing role.

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 focuses on developing, qualifying, and implementing analytical methods for biologics drug products, including monoclonal proteins and other complex therapeutic proteins. It involves assay development, benchmarking, technical leadership, and data interpretation within a pharmaceutical R&D setting.

This role is responsible for developing and implementing CMC regulatory strategies for pharmaceutical pipeline products, ensuring compliance with global regulations and preparing CMC dossiers for submission. It involves serving as a CMC Product Lead, assessing regulatory success probabilities, and managing regulatory milestones throughout product development.

The Field Access Manager (FAM) is responsible for educating healthcare professionals and organizations on access-related issues, including patient support programs, reimbursement, and compliance with healthcare regulations. This remote/field-based role analyzes access trends, addresses barriers to patient access, and collaborates cross-functionally to ensure timely patient access to therapy.

The Sourcing Specialist is responsible for sourcing and negotiating the supply of various materials and services, with a primary focus on direct materials such as packaging, tooling, equipment, and associated spare parts and installation services. The role involves executing global category sourcing strategy, managing vendors, and achieving key performance indicators for the procurement business. It requires strong analytical, negotiation, and stakeholder management skills within a matrix environment.