Merck

Seeking an Associate Principal Scientist for the Process Analytical Technologies (PAT) team to lead the development, validation, and implementation of in-line, on-line, and at-line PAT solutions for small- and large-molecule modalities in pharmaceutical development and manufacturing. Responsibilities include technical leadership, designing analytical platforms, developing and validating PAT methods, leading scale-up and technology transfer, creating integrated control strategies, preparing documentation for regulatory submissions, and interacting with regulatory agencies.

The Director, Strategic Planning role at Merck focuses on developing and driving enterprise strategy, particularly within Oncology R&D. This involves identifying strategic imperatives, framing and assessing initiatives, developing data-based insights, and collaborating with senior leaders and cross-functional teams to implement changes and evolve capabilities. The role requires a PhD or MD with significant strategy consulting or biopharma R&D strategy experience, strong analytical and communication skills, and leadership abilities.

This role is for a Technical Lead in Small Molecule API Chemical Technical Operations, supporting drug substance tech transfer and commercial manufacturing within an external manufacturing network. Responsibilities include managing the technical interface with external partners, providing process support, evaluating change requests, managing risks, and overseeing new product introductions and technical transfers. The role requires a technical degree with significant pharmaceutical industry experience in API manufacturing.

Merck is seeking a Maintenance Mechanic (m/f/d) for their GMP-regulated production site in Friesoythe, Germany. The role involves managing spare parts, performing maintenance and repair work on production and utility systems, and ensuring the availability of technical infrastructure. The ideal candidate will have a technical background in mechanics, plant construction, and maintenance, with experience in a GMP environment.

This role leads Supply Chain Management for a biopharmaceutical production site, focusing on end-to-end planning, inventory management, warehouse and distribution, and team leadership. It requires experience in logistics, supply chain, and personnel management, with a strong emphasis on process optimization and stakeholder communication within a GMP-regulated environment.

Merck is seeking a Production Improvement Officer in Boxmeer, NLD, to optimize production lines and processes within a GMP-certified environment. The role focuses on safety, quality, delivery reliability, and cost reduction through a data-driven approach, lean management, and root cause analysis. Responsibilities include implementing sustainable improvements, managing standards, and collaborating with various teams.

This role supports the Learning & Development team in creating, maintaining, and administering medical and didactic content for pharmaceutical products and indications. Responsibilities include content creation (text, presentation, video, social media), translation, managing a Learning Experience Platform (SANA), overseeing the medical review process, organizing seminars, and managing smaller projects like video design. The role requires a science background (medicine, biology, pharmacy, etc.), strong German and English skills, and a meticulous approach to medical accuracy. Experience with digital learning content creation and AI applications is a plus.

Senior Distribution Coordinator role at Merck, focusing on managing complex international logistics and supply chain operations for animal health products. Responsibilities include booking and monitoring shipments, ensuring trade compliance, preparing shipping documents, and leading improvement initiatives. Requires a Bachelor's degree in Supply Chain or Logistics, at least three years of experience, and strong knowledge of international forwarding and customs.

The External Affairs Manager will be part of the Policy and Corporate Communications Team, responsible for strategic focus and implementation in political work within the Austrian healthcare system, with a particular emphasis on oncology (early detection, screening, and care optimization). This role involves engaging with external stakeholders, analyzing the health policy environment, representing the company, and collaborating across various internal and external teams.

Manager for Quality Control in a pharmaceutical manufacturing facility, focusing on leading teams, ensuring compliance with global policies and regulatory requirements, managing laboratory operations, budgets, and driving continuous improvement through lean projects. Requires a Bachelor's Degree in Engineering or Science and 5+ years of pharma industry experience.

This role is responsible for driving performance and maximizing the Oncology portfolio by identifying and executing growth opportunities. It involves strategic planning, data analytics, project management, and operational leadership within the pharmaceutical industry, focusing on commercial operations and business strategy.

Merck is seeking a Qualification Expert for Packaging Equipment (m/f/d) at their Vienna, Austria site. This role focuses on the planning, preparation, and execution of qualifications and re-qualifications for packaging lines and related equipment within a biopharmaceutical manufacturing environment. The position requires strong knowledge of GMP, packaging technology, and regulatory guidelines, with responsibilities including documentation, testing, auditing, and project participation.

This role is a customer support position focused on providing technical assistance and training for a monitoring solution. It involves handling customer inquiries, troubleshooting issues, and maintaining knowledge articles. The role is not directly involved in AI/ML development or research.

The Medical Science Liaison (MSL) in Oncology acts as a scientific bridge between Merck and the external medical community, engaging in scientific exchange with medical leaders. The role involves providing balanced, factual scientific information about disease areas and Company products, supporting clinical trials, and gathering scientific insights. Responsibilities include non-promotional scientific exchange, responding to unsolicited requests, facilitating clinical trials and investigator-initiated studies, and supporting the generation of local data. The role requires a PhD in a health or life science field, strong scientific knowledge, excellent communication and analytical skills, and understanding of local pharmaceutical industry guidelines and regulations.

The Associate Principal Scientist, Epidemiologist role at Merck focuses on pharmacoepidemiologic planning and study execution for assigned products. This role involves designing, conducting, and analyzing epidemiologic research, providing scientific oversight, and contributing to the company's scientific prestige through publications and presentations. The position requires a PhD or MD with research training in Epidemiology, extensive experience in leading epidemiologic projects, and a strong publication record. The role is within the healthcare domain and involves research functions.

Associate Director, Quality Systems & Compliance role at Merck, focusing on Design Controls within the Device Quality & Regulatory team. This position supports the Manufacturing Division's QMS, leads continuous improvement initiatives, and ensures compliance with cGMP, ISO 13485, and global health authority regulations for pharmaceutical and medical device products. The role involves collaboration with cross-functional teams, oversight of procedures, and acting as a subject matter expert in quality management systems.

Executive Director, Chemistry, Manufacturing, Control for Biologics (Biologics-CMC) at Merck, responsible for managing a team, ensuring rigor in CMC regulatory strategy, and delivering high-quality CMC submissions for late-phase new modality biologics products. This role involves driving global alignment and execution across various departments to ensure compliance and availability of programs to patients.

Co-op program in Merck's Manufacturing Division, focusing on global technical support for vaccine and biologics manufacturing. Roles involve late-stage process development, commercialization, tech transfer, and commercial manufacturing support, utilizing engineering, chemistry, and data science tools.

The Regional Medical Scientific Director (RMSD) is a therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.

This role is for a 24x7 Security Operations Analyst responsible for managing and supporting IT security platforms, triaging alerts, and resolving security incidents. It involves collaboration with engineering and operations teams, maintaining security tools, and ensuring operational continuity.

Merck is seeking a Business Development and Alliance Management Associate Director in Tokyo, Japan, to develop and implement business development strategies, identify partnership opportunities, and manage alliances to maximize the company's product portfolio within the healthcare industry. The role requires strong strategic planning, negotiation, and communication skills, with a focus on the biotech/pharmaceutical sector.

Merck is seeking a Senior Maintenance Technician for a new factory construction project. The role involves performing maintenance on production lines, troubleshooting technical issues, and contributing to the reliability and improvement of machinery. The position requires a technical background, adherence to GMP and safety standards, and collaboration with other teams. The role is hands-on and involves on-call duties.

This role focuses on developing and maintaining manufacturing process models using discrete event simulation for shopfloor operations management, including finite scheduling and productivity analysis. It involves configuration, testing, documentation, and providing technical support for optimization and data analysis, primarily using SQL.

The Associate Principal Scientist will focus on chromatographic isolation of pharmaceutical API and impurities from analytical scale to semi-prep scale and prep scale, supporting various pharmaceutical modalities. This role involves partnering with process chemists and analytical scientists to deploy efficient chemical isolation methods and establish innovative purification workflows.

The Regional Medical Scientific Director (RMSD) is a therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies.

The Regional Medical Scientific Director is a credentialed therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.

This role is for a Regional Medical Scientific Director in Ophthalmology at Merck. The primary focus is on engaging with Scientific Leaders (SLs) to exchange scientific and medical information, support research initiatives, and gather insights. The role requires deep therapeutic expertise and adherence to regulatory guidelines.

The Regional Medical Scientific Director (RMSD) is a therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.

Financial Analyst Cost Accounting role at Merck, responsible for maintaining, reviewing, reporting, and analyzing inventory, production, and product cost data. Supports monthly accounting close and management cycles, ensuring compliance with US GAAP and S404 requirements. Requires a Bachelor's or Master's degree in finance, business administration, or economics, with 3-5 years of relevant finance experience, preferably in a manufacturing environment. Strong analytical skills, experience with SAP, and customer focus are essential.

This role is a General Affairs Specialist Office Support position at Merck, focused on supporting employees with disabilities through job coaching and employment support services. The primary responsibilities include business support tasks, cafe operations, social skill development, collaboration with external parties, and planning/execution of disability hiring initiatives. It requires strong communication, problem-solving, and ethical conduct.

Administrative intern role supporting clinical trials at Merck, focusing on logistics, document management, and meeting arrangements. Requires current student status in a healthcare-related field with availability for part-time work over a specific period.

This role is for a Quality Assurance Officer at Merck, focused on ensuring batch documentation is prepared, reviewed, and released on schedule to meet production, testing, and export requirements. It involves supporting QA systems, maintaining compliance with regulatory and corporate standards (GMP/GLP), and facilitating product release.

Executive Director, Microbiology at Merck responsible for strategic and technical leadership of the Microbiology Network supporting clinical development candidates. This includes oversight of GMP release, stability, environmental monitoring, analytical method transfers, regulatory filings, and implementation of new analytical technologies. The role involves significant cross-functional collaboration, team management (approx. 60 scientists), budget management, and ensuring GMP compliance and scientific excellence.

Merck is seeking a Senior Director (Senior Principal Scientist) in Translational Medicine, Immunology. This role focuses on planning and managing the early stages of drug development, translating preclinical science into compounds for clinical assessment. Responsibilities include contributing to target identification, developing biomarker strategies, and executing early clinical development and pharmacology strategies. The ideal candidate is a physician-scientist with experience in pharmaceutical R&D, clinical research, and immunology, particularly in areas like Dermatology, Rheumatology, or Gastroenterology.

Merck is seeking a Data Engineer for their R&D IT Informatics team to build and maintain dashboards and data solutions for Animal Health R&D. The role involves translating scientific questions into data-driven insights, collaborating with scientists, and developing ETL pipelines and data models on cloud platforms. Experience with BI tools, SQL, Python, and cloud data platforms is required.

This role is responsible for managing and executing labeling operational tasks within the pharmaceutical industry, ensuring compliance with regulatory standards and supporting product launches. It involves serving as a point of contact, processing updates, performing quality checks, and collaborating with cross-functional teams.

This role supports the end-to-end meeting services process for global congresses and sponsorships, focusing on financial operations, compliance, and vendor management within a business service center environment. It requires experience in basic accounting or P2P/O2C/R2R processes, intermediate Excel skills, and strong attention to detail.

Associate Director of Drug Substance Commercialisation at Merck, responsible for technical support, process development, scale-up, and production of clinical and commercial APIs. The role involves leading teams, ensuring regulatory compliance, and driving process improvements within a commercialization facility.

Associate Director of Medical Affairs for Respiratory in Latin America, responsible for developing and executing the Country Medical Affairs Plan, engaging with scientific leaders, and collaborating cross-functionally to improve patient outcomes and access to treatments. This role involves strategic planning, scientific information exchange, budget management, and supporting clinical development programs.

The role involves installing, maintaining, testing, and repairing HEPA filtration equipment in a pharmaceutical manufacturing environment. Responsibilities include performing HEPA certifications, leak checks, velocity spot checks, particle counts, and assisting with HVAC system troubleshooting. The technician must comply with operating procedures, company, and government regulations, including Good Manufacturing Practices (GMP). The role requires experience with specific testing equipment and potentially maintaining business systems like EAM.

The CRM & SFE Specialist owns the CRM and Sales Force Effectiveness (SFE) capability and associated ways of working, including governance, standards, and adoption. The role is accountable for system reliability, data quality, and user adoption, ensuring compliant, high value CRM use across markets. The specialist continuously enhances CRM capabilities to support SFE processes, omnichannel engagement, and efficient commercial execution. As the single point of accountability for CRM and SFE across the assigned markets, the role partners closely with commercial teams and key stakeholders. This is a hands-on role requiring expertise in Veeva CRM, Salesforce, Salesforce Marketing Cloud and related systems. The CRM & SFE Specialist acts as the local Subject Matter Expert, performs system configuration and updates, manages tagging and taxonomy, supports omnichannel journey execution, and raises and manages IT service requests on behalf of the business.

Administrative Associate role at Merck Animal Health in Australia, providing comprehensive administrative and operational support to directors and senior managers. Responsibilities include stakeholder management, privacy coordination, meeting and travel arrangements, team engagement, and general administrative tasks such as contract management, expense reconciliation, and invoice processing. Requires tertiary qualifications, prior administrative experience, strong organizational skills, proficiency in MS Office, and excellent communication.

Merck is seeking a Building Automation Engineer for their Digital Manufacturing Organization in Haarlem, NLD. The role involves technical management of building automation systems, including upgrades, improvements, and issue resolution. The ideal candidate will have experience with Johnson Controls or Siemens systems, automation in a GMP environment, and a HBO or equivalent education. Knowledge of PLCs and Siemens TIA-portal is a plus.

This role is responsible for regulatory affairs in Vietnam, ensuring compliance with local regulations for company products. Key activities include preparing and submitting documentation to regulatory agencies, monitoring regulations, reviewing labeling, and acting as a pharmacovigilance contact.

Senior Process Engineer at Merck in Singapore, responsible for supporting or leading new product introductions to the site. This includes process and equipment comparisons, raw material introduction, development studies, manufacturing of clinical supplies, cleaning process development/validation, and technician training. The role involves authoring PPQ protocols and reports, understanding product development, scale-up, and technical transfer, and providing technical writing for change requests and CMC sections. It also includes designing and executing experiments, providing technical guidance for capital projects and facility start-up, troubleshooting deviations and complaints, supporting compliance activities like audits, and managing product portfolio activities such as documentation updates and validation. The role also supports routine manufacturing by providing ongoing technical support, participating in improvement initiatives, and monitoring process performance. Experience with statistical analysis, risk assessment, and understanding of product critical parameters is required.

This role involves engaging with scientific leaders to exchange medical and scientific information, support research initiatives, and gather insights within the ophthalmology therapeutic area. The Regional Medical Scientific Director acts as a disease expert, providing balanced information and facilitating understanding of company research strategies and clinical trials.

The Regional Medical Scientific Director (RMSD) is a credentialed therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.