Clinical Research Manager for Ophthalmology at Merck, responsible for end-to-end performance and project management of assigned clinical trial protocols within a country, ensuring compliance with regulations, company policies, and quality standards. This role involves planning, driving execution, managing local study teams, risk management, system compliance, vendor collaboration, and representing the company with investigators.

The Principal Scientist, Oral Formulation Sciences at Merck will lead CMC project teams and the formulation development of new chemical entities. This role involves designing, developing, and scaling-up formulation, device, and manufacturing processes, driving new technology strategy, and mentoring technical staff. The scientist will also spearhead due diligence, coordinate technology development, and collaborate across functional areas to develop novel drug delivery technologies. The position requires a Ph.D. with at least 8 years of experience or an M.S. with 10 years, or a B.S. with 14 years, in a relevant scientific discipline.

This role is for a Specialist, Safety & Environment within Merck's EHS team, focusing on developing, implementing, and maintaining EHS systems to ensure compliance with legal and corporate standards in a highly regulated pharmaceutical manufacturing environment. Responsibilities include providing technical guidance, conducting evaluations and audits, managing EHS queries, and ensuring site environmental compliance.

This co-op role supports the development of translational in vitro models for therapeutic areas, focusing on iPSC-derived systems and assay execution. Responsibilities include cell culture maintenance, assay workflow execution, data entry and analysis, and assisting with assay optimization. The role requires prior laboratory experience and strong organizational and communication skills.

Internship opportunity within the Large Molecules Analytical Technical Solutions (ATS-bio) department focused on optimizing biological laboratory assays to determine the safety and efficacy of vaccines. The intern will be responsible for developing a method to assess the effectiveness and quality of biological critical reagents (BCRs) used in quality control tests for vaccine release testing. This involves using kinetic binding evaluations with interferometry and performing related laboratory assays, with a focus on assay component optimization, stability, and troubleshooting.

This role focuses on designing and implementing integration solutions using SAP BTP and related middleware, ensuring seamless connectivity between SAP and non-SAP systems. It involves administration, monitoring, and optimization of integration processes, with a strong emphasis on security and regulatory compliance.

This is an alternance (internship) position at Merck for an Assistant Project Manager in the Commercial Access department, focusing on the hospital market. The role involves commercial analysis, developing tracking tools for field and headquarters teams, analyzing qualitative subjects related to commercial strategies, and coordinating with business units. It also includes project management support, preparing for seminars and team meetings, and working with various stakeholders. The ideal candidate has a scientific background with a specialization in commerce/marketing, strong organizational and interpersonal skills, and proficiency in digital tools like Qlik. Pharmaceutical or hospital environment experience is a plus.

Key Account Manager responsible for end-to-end management of strategically relevant national and international veterinary corporate clients within the Companion Animal Business Unit in Switzerland. Ensures sustainable growth, strong long-term customer partnerships, and consistent implementation of corporate account strategies.

This role is for an Improvement Engineer at Merck's Animal Health manufacturing site in New Zealand. The engineer will lead complex problem-solving initiatives, drive process improvements, and execute technical activities to ensure safe, compliant, and cost-effective product supply. Responsibilities include acting as a technical expert, identifying improvements, leading projects, analyzing data, and coaching colleagues within a GMP-regulated environment.

Junior Manager Operations role at Merck, focusing on daily production, safety, quality, and people management in a pharmaceutical manufacturing environment. Responsibilities include leading operators, managing improvement projects, ensuring GMP compliance, and meeting production/cost targets.

Lead the device development strategy for drug-device combination products, ensuring quality and compliance from concept to launch. This role involves managing cross-functional teams, overseeing technical aspects of device design and manufacturing, and authoring regulatory submissions within the pharmaceutical and medical device industries.

Distinguished Scientist (Executive Director) and Product Development Team (PDT) Lead for Oncology Global Clinical Development, focusing on Thoracic Oncology. Responsibilities include planning and directing clinical research activities, managing the entire cycle of clinical development from strategy to regulatory reporting and publication, and providing scientific leadership. Requires M.D or M.D./Ph.D. with industry experience in Thoracic Oncology and drug development.

Associate Director role focused on leading digital transformation for industrial data platforms in global manufacturing environments, specifically supporting AVEVA PI Systems and related components. The role involves technical leadership, execution, and troubleshooting to improve shop-floor data quality, productivity, and decision-making in pharmaceutical manufacturing.

Entry-level automation specialist role in a pharmaceutical manufacturing environment, focusing on hands-on technical support for automated systems, troubleshooting, and ensuring compliance with cGMPs. The role involves working on PLCs, DCS, and OEM platforms to maintain manufacturing yield, cycle time, and reliability.

Chemical Engineer role focused on process development, scale-up, and manufacturing support for pharmaceutical products within Merck's global pharmaceutical and commercialization organization. The role involves working on Drug Product projects from Phase IIb through regulatory filings and commercial launch, with a focus on Active Pharmaceutical Ingredients (API) and Oral Solid Dose (OSD) products.

This role focuses on translating global evidence strategies into regional execution plans for healthcare products in Mid-Europe, supporting access, reimbursement, and value demonstration through health economics, outcomes research, and real-world evidence initiatives.

This role is for a Maintenance Technician in an industrial setting, responsible for ensuring the reliability, safety, and availability of equipment and facilities. Key responsibilities include prioritizing EHS, performing preventive and corrective maintenance, collaborating with operations, using CMMS tools, and interpreting technical documentation. The role requires a technical degree in industrial maintenance or equivalent and at least 3 years of experience in industrial maintenance, with knowledge of electrical, pneumatic, general mechanical systems, and HVAC. Valued skills include problem-solving, automation, PLC knowledge, GMP, CMMS (SAP), and SCADA systems.

This role is for a Technical Planner/Work Preparer in the pharmaceutical industry, focusing on ensuring the optimal reliability and technical availability of production equipment within a cleanroom environment. Responsibilities include analyzing maintenance processes, planning and coordinating maintenance activities, advising on technical aspects of projects, and documenting procedures. The role requires a technical education at HBO level and experience in a similar role within the pharmaceutical, chemical, or food industry.

Associate Director, Regional Procurement leads strategic procurement initiatives supporting manufacturing operations and growth across multiple sites in a regulated biopharmaceutical environment. Drives value through sourcing strategies, supplier performance, risk mitigation, and stakeholder partnership.

This role is responsible for ensuring the scientific, ethical, and regulatory integrity of all medical-scientific information activities within the company, in full compliance with AIFA regulations, the Farmindustria Code of Ethics, and internal policies. It oversees medical review activities for promotional and external materials, disease awareness campaigns, and other product- or therapy area-related communications, while also serving as the accountable leader for the local Designated Point of Contact for medical, safety, and product quality inquiries. In addition, this role leads and develops a team by fostering a collaborative, inclusive, and high-performing environment grounded in constructive feedback, effective delegation, and strong interpersonal awareness.

This role focuses on network capacity planning and data engineering within an enterprise environment. The Senior Network Capacity & Data Engineer will analyze network traffic, utilization, and performance metrics using predictive analysis to identify bottlenecks and areas for improvement. Responsibilities include collaborating with various teams for capacity planning, planning hardware upgrades, providing reports on KPIs and utilization, mitigating risks related to capacity failures, and participating in cross-functional projects. The role requires strong engineering or operations experience with global network infrastructure components, experience in analytics and data-driven decision making, and familiarity with network monitoring and observability tools. Programming experience in Python, Java, or JavaScript is also required.

This role is responsible for ensuring products managed by External Quality Assurance (EQA) are manufactured, packaged, analyzed, released, stored, and distributed in conformance with all applicable regulatory requirements, regulatory filings, and company policies. The Senior Specialist acts as a Qualified Person (QP) for batch release in the EU market and manages deviations, complaints, and change controls.

This is an apprenticeship role in Quality Design and R&D Laboratories at Merck, focusing on product development within an industrial environment. The role involves supporting project teams with quality standards, implementing design quality tools, identifying non-conformities, participating in corrective actions, and contributing to audits and continuous improvement. It is a 3-year apprenticeship starting in September 2026.

Associate Director, Launch Excellence role at Merck, focusing on shaping and executing product launches in the pharmaceutical industry. This role translates enterprise priorities into launch strategies, manages cross-functional stakeholders, and drives launch execution to accelerate impact. It involves developing launch frameworks, best practices, and serving as a PMO for priority assets.

The Associate Director, Launch Excellence PMO at Merck will support new launch brands by managing plans, tracking actions, and identifying risks. This role involves cross-functional coordination to ensure readiness and drive execution, with an emphasis on learning and improving launch approaches.

Director, External Large Molecule Analytical role at Merck, focusing on global analytical technical oversight for large molecule commercial products in China. This involves direct contact with government laboratories and contract organizations to ensure robust local testing programs and uninterrupted supply of biologics and vaccines. Responsibilities include establishing relationships, supporting test methods, troubleshooting, facilitating logistics, participating in cross-functional teams, communicating challenges, and influencing regulatory compendia updates. Requires a Bachelor's degree with 12 years of experience or Master's with 8 years or PhD with 4 years in analytical testing, development, transfer, or validation within the biopharmaceutical industry.

Associate Specialist in Quality Assurance at Merck, focusing on batch review, disposition, deviation management, and change control within a regulated pharmaceutical manufacturing environment. Requires knowledge of GMP and pharmaceutical regulatory requirements, with a minimum of 1-3 years of experience. This role is part of a career conversion program for Singaporeans/PRs.

This role provides statistical support and leadership for clinical safety data evaluation, collaborating with cross-functional teams throughout the drug development lifecycle. It involves designing, developing, and evaluating processes, methods, and tools for safety data analysis, and staying current with regulatory guidance and innovative statistical research.

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.

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.

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.

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.

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.