Principal Scientist, DSCS Digital Technologies-Laboratory Automation, Time Series Data Strategy (Hybrid) Merck & Co IncPrincipal Scientist, DSCS Digital Technologies-Laboratory Automation, Time Series Data Strategy (Hybrid)Rahway, NJ$173,200–$272,600 / yearThe chosen candidate will lead strategy, architecture, and delivery for time series data capabilities across the DSCS community, including integrating various time-series data streams into state-of-the-art, contextualized content that can be consumed by downstream data products, business data platforms, lineage solutions, AI-driven modeling workflows, dashboards, and scientific decision-making tools. This role will help establish a comprehensive strategy with clear definitions, prioritization principles, and scalable platforms across real-time, near-time, and post-batch efforts that align short-term business solutions with sustainable long-term enterprise strategies.
Dir, Specialty & Pharma Communications - New Products (Ophthalmology) Merck & Co IncDir, Specialty & Pharma Communications - New Products (Ophthalmology)Rahway, NJ$173,200–$272,600 / yearRequired Skills: Collaborative Spirit, Content Creation, Data Analysis, Event Management, Internal Communications, Marketing Communications Planning, Media Publishing, Media Relations, Medical Communications, Online Content Development, Public Health Communications, Public Speaking, Reputation Management, Strategic Planning, Trade Media Relations. Responsibilities include but will not be limited to the following key activities: Manage branded and unbranded communications activities in support of our company ophthalmology portfolio, with a heavy emphasis on milestone communications (regulatory approvals, data releases, medical meeting communications).
Director, Strategic Planning Merck & Co IncDirector, Strategic PlanningRahway, NJ$173,200–$272,600 / yearRequired Skills: Analytical Tools, Business Development, Business Intelligence (BI), Competitive Intelligence (CI), Data-Driven Decision Making, Developing Proposals, Drug Discovery Process, Environmental Scanning, Gastroenterology, Immunology, Inflammatory Bowel Diseases, Influencing Skills, Pharmaceutical Industry, Research Programs, Results-Oriented, Stakeholder Management, Strategic Thinking. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Associate Director, Global Data Management and Standards - Business Operations - Hybrid Merck & Co IncAssociate Director, Global Data Management and Standards - Business Operations - HybridRahway, NJ$142,400–$224,100 / yearThe Associate Director partners with business leaders and key stakeholders to lead change management efforts, develop and execute communication strategies that promote transparency and stakeholder engagement, and champion learning and development initiatives that build organizational capabilities and support adoption of new processes, technologies, and ways of working. Manage real-time workload balancing, capacity, and compliance-driven case allocation across geographies within the functional area to ensure balanced operations, on-time delivery, and business continuity through holidays, resource availability, and demand peaks.
Filling Set-up Sr. Technician, Operations - Onsite Merck & Co IncFilling Set-up Sr. Technician, Operations - OnsiteRahway, NJ$68,000–$107,000 / yearRequired Skills: Biopharmaceutical Manufacturing, Clinical Trials Operations, FDA Regulations, GMP Compliance, Good Manufacturing Practices (GMP), Laboratory Techniques, Manufacturing Quality Control, Manufacturing Support, Master Batch Records, Material Selection, Production Planning, Safety Protocols, SAP Enterprise Resource Planning (ERP), SAP Systems, Shift Work, Visual Inspections. Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.
Sr. Director, Materials Science Merck & Co IncSr. Director, Materials ScienceRahway, NJ$173,200–$272,600 / yearRequired Skills: Analytical Method Development, Analytical Thinking, Cross-Cultural Teams, Data Integrity, Drug Development, Materials Engineering, Materials Science, Materials Technology, Molecular Structure, Multidisciplinary Teamwork, Operational Excellence, Organizational Compliance, People Leadership, Technical Leadership. This leader is responsible for providing strategic and technical leadership for materials characterization methodologies, phase screening platforms, and extraneous matter investigations to enable deep understanding of drug substances and drug products and successful advancement of small molecules, biologics, and vaccines from discovery through development and commercial launch.
Powerhouse Assistant Chief Engineer Merck & Co IncPowerhouse Assistant Chief EngineerRahway, NJ$106,200–$167,200 / yearMaintain operational control of the Steam Plant (up to 900 psi), Electric Cogeneration Plant (15 MW capacity), Demineralized Water Plant, compressed air systems, potable water distribution systems, and process cooling tower operations. The Assistant Chief Engineer reports to the Associate Director of Engineering and is responsible for supervising Power Plant operating personnel while ensuring the safe, reliable, and efficient production and distribution of utility services supporting the Rahway site.
Director Global Market Access Oncology - New Product Merck & Co IncDirector Global Market Access Oncology - New ProductRahway, NJ$190,800–$300,300 / yearThe Director, Oncology Global Market Access - New Product, will report directly to the Associate Vice President, oGMAx and will be responsible to develop and lead the global access strategy development and execution for a new oncology pipeline asset with an extensive clinical development program across multiple indications. Engage with Product Development Teams to ensure clinical trial designs (e.g., endpoints, comparators, label language) and value evidence plans are thoughtfully informed by payer requirements and access objectives.
Executive Director, Patient Experience and Acceleration Merck & Co IncExecutive Director, Patient Experience and AccelerationRahway, NJ$255,800–$402,700 / yearRequired Skills: Agile Methodology, Agile Methodology, Biopharmaceutical Industry, CiviCRM, Cross-Cultural Awareness, Customer Relationship Management (CRM) Software, Decision Making, Developing Pricing Strategies, Direct Marketing, Extensive Traveling, Healthcare Innovation, Human Diseases, Interpersonal Relationships, Latin American Markets, Market Research, Organizational Performance Management, Patient Assistance Programs, People Leadership, Pricing Processes, Product Development, Product Management, Stakeholder Engagement, Stakeholder Management, Strategic Management, Strategic Thinking {+ 2 more}. Necessary Skills and Competencies: 12+ years in biopharma patient services, commercial operations, or hub/vendor management, with experience leading patient support organizations or CoEs at multi-brand across hub, access, affordability, adherence, and FRM.
Executive Director, Direct-to-Patient Platform Merck & Co IncExecutive Director, Direct-to-Patient PlatformRahway, NJ$255,800–$402,700 / yearRequired Skills: Cross-Cultural Awareness, Cross-Cultural Awareness, Decision Making, Developing Pricing Strategies, Direct Marketing, E-Commerce, Extensive Traveling, Human Resource Management, Interpersonal Relationships, Latin American Markets, Logistics Management, Market Research, Medical Records Management, Operating Models, Operational Performance Management (PM), Organizational Performance Management, Patient Assistance Programs, People Leadership, Pharmacy Operations, Pricing Processes, Product Development, Product Management, Regulatory Requirements, Retail Pharmacy, Strategic Thinking {+ 2 more}. Necessary Skills and Competencies: 12+ years in biopharma patient services, specialty pharmacy operations, or channel/fulfillment operations - or equivalent experience in direct-to-consumer logistics, e-commerce fulfillment, or telehealth operations - with prior experience leading platform capabilities: operating model design, vendor governance, and performance management.
Principal Scientist, Pharmaceutical Analytical Sciences Merck & Co IncPrincipal Scientist, Pharmaceutical Analytical SciencesRahway, NJ$156,900–$247,000 / yearRequired Skills: Analytical Characterization, Analytical Chemistry, Analytical Method Development, Assay Development, Bioanalysis, Chromatographic Techniques, Chromatography, Clinical Judgment, Clinical Trials, Conducting Experiments, Data Science, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Method Validation, Product Development, Scientific Study Design, Stability Testing. Your main responsibilities, in not particular order and by no means complete, include: Driving our company's Pipeline: Leading analytical teams driving the development of drugs in our company's pipeline, with a deep understanding of product development from early stage through commercialization.
Filling Set-up Sr. Technician, Operations (2nd Shift) - Onsite Merck & Co IncFilling Set-up Sr. Technician, Operations (2nd Shift) - OnsiteRahway, NJ$68,000–$107,000 / yearRequired Skills: Applied Research, Applied Research, Biopharmaceutical Manufacturing, CNC Operations, Computer Literacy, Data Analysis, Enterprise Resource Planning (ERP), Enterprise Resource Planning (ERP) Systems, FDA Regulations, GMP Compliance, Good Manufacturing Practices (GMP), Laboratory Techniques, Manufacturing Quality Control, Manufacturing Support, Master Batch Records, Material Selection, Pharmaceutical Process Development, Preventive Action, Production Planning, Regulatory Compliance, Safety Protocols, SAP Enterprise Resource Planning (ERP), SAP Systems, Shift Work, Sterile Procedures {+ 1 more}. Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.
Director of GMP Analytical, Pharmaceutical Analytical Sciences Merck & Co IncDirector of GMP Analytical, Pharmaceutical Analytical SciencesRahway, NJ$173,200–$272,600 / yearRequired Skills: Analytical Method Development, Analytical Reports, Analytical Testing, Biologics License Application (BLA), Chromatographic Techniques, Compliance Oversight, Dosage Forms, GMP Compliance, Inspection Readiness, People Leadership, Pharmaceutical Management, Process Analytical Technology (PAT), Project Management, Regulatory Compliance, Regulatory Submissions, Risk Analysis, Risk Assessments, Risk Evaluation And Mitigation Strategy (REMS), Spectroscopy, Talent Development, Team Leadership, Technical Writing. In this role, the Director will lead a team of scientists in Rahway supporting various GMP analytical activities including method validation, clinical release, and stability testing for drug substance and drug product across the entirety of our small molecule clinical portfolio (oral solid dosage forms and sterile liquids).
Toledo, OH Territory Manager Merck & Co IncToledo, OH Territory ManagerRahway, NJ$96,200–$151,400 / yearThis position is responsible for working in their respective territory to understand and identify veterinary clinic, shelter facility, and corporate account customer needs, by selling our Company's Animal Health division, Companion Animal product portfolio, supporting pull-through activities relative to the customer strategy, and ensuring that our Company's Animal Health division is viewed as bringing value and technical innovations aligned to our strategic focus - The Science of Healthier Animals. Primary point of contact for assigned customers, meet with key personnel/decision makers to understand practice structure, business model, key influencers (Owner/Practice Manager/Key Tech/Associate Vet/Front office staff), customer needs and identifies business opportunities.
Director, Chemical Engineering R&D Merck & Co IncDirector, Chemical Engineering R&DRahway, NJ$173,200–$272,600 / yearRequired Skills: Chemical Engineering, Chemical Technology, Clinical Manufacturing, Collaborative Communications, Diversity and Inclusion (D&I), Drug Development, Good Manufacturing Practices (GMP), Pharmaceutical Process Development, Pharmaceutical Process Engineering, Process Manufacturing, Project Portfolio Management (PPM), Regulatory Compliance, Technical Leadership, Technology Transfer, Vaccine Manufacturing. Critical tasks involve technical and strategic oversight of chemical engineering staff who directly contribute to the development, characterization and scale-up of various unit operations for manufacturing processes, including batch and continuous reactions, crystallizations, extractions, membrane separations, distillation, filtration and drying.
Associate Director - CMC Data Steward - DSCS Digital Merck & Co IncAssociate Director - CMC Data Steward - DSCS DigitalRahway, NJ$129,000–$203,100 / yearDSCS Digital Technologies is seeking an experienced Data Steward to drive the quality, consistency, usability, and business value of critical data assets across the Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) landscape. Partner with Manufacturing, R&D, Quality, Supply Chain, Regulatory, and IT teams to ensure data assets are appropriately governed for regulatory submissions and inspections, advanced analytics, machine learning, predictive modeling, and AI applications.
Director Global Oncology Market Access, Sac-TMT and Women's Cancers Merck & Co IncDirector Global Oncology Market Access, Sac-TMT and Women's CancersRahway, NJ$190,800–$300,300 / yearRequired Skills: Collaboration, Commercial Acumen, Cross-Cultural Awareness, Data Analysis, Global Market Access (GMA), Market Access, Market Research, Oncology Marketing, Patient Access, Payer Reimbursement, Strategic Planning, Strategic Thinking. Engage with Product Development Teams (including Clinical, V&I, Regulatory Affairs) to ensure clinical trial designs (e.g., endpoints, comparators, label language) and value evidence plans are thoughtfully informed by payer requirements and access objectives.
Senior Scientist, Biocatalysis Merck & Co IncSenior Scientist, BiocatalysisRahway, NJ$117,000–$184,200 / yearThey will give scientific presentations internally and externally, contribute to publications and patents, contribute to defining the scientific strategy on programs, and develop new approaches that accelerate research and development while advancing the fields of enzyme engineering and biocatalysis. The Biocatalysis group within the Small Molecule Process Research & Development Department in Rahway, New Jersey is seeking a Senior Scientist to expand our capabilities to design and deliver world-class biocatalytic solutions that enable the development of medicines.
Prin. Scientist, Clinical Research Merck & Co IncPrin. Scientist, Clinical ResearchRahway, NJ$190,800–$300,300 / yearInterface broadly with key functions including Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research throughout research sites around the world. Contributing to the identification of novel targets by partnering with discovery research teams to bring a clinical perspective into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in order to justify investment in clinical development programs.
Associate Director, Quantitative Pharmacology and Pharmacometrics - Immuno-Oncology (QP2‑IO) Merck & Co IncAssociate Director, Quantitative Pharmacology and Pharmacometrics - Immuno-Oncology (QP2‑IO)Rahway, NJRemote$156,900–$247,000 / yearWe are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs)), and representing QP2-IO at regulatory meetings.