Full-stack Engineer

• Provide end‑to‑end technical leadership for facility‑fit assessments for both inline and New Product Introduction (NPI) programs
• Lead the identification, prioritization, and resolution of engineering issues arising during facility‑fit activities
• Deliver strong technical oversight to ensure technical excellence and right‑first‑time execution during process transfers
• Act as a subject matter expert (SME) in biologics process equipment
• Serve as an SME in the development of digital twin solutions and strategic improvements
• Make recommendations for site equipment investments
• Provide technical input to upstream and downstream platform definitions
• Collaborate closely with broader Science & Technology (S&T) functions
• Establish and lead a small, focused team of engineers
• Develop, mentor, and coach engineering team members

Process and Technical Engineering Lead

Business Intelligence Analyst

• Lead the strategy, development, and governance of DSCS-wide analytics, data products, and business intelligence capabilities.
• Accelerate data-driven decision-making across functions by providing high-value insights, modern BI solutions, and scalable digital platforms.
• Define the vision for agentic business intelligence, lead a team of engineers/ analysts, standardize analytics workflows, and partner cross-functionally.
• Develop and own the Agentic Business Intelligence Strategy aligned with enterprise digital transformation goals.
• Ensure capabilities scale with business growth and scientific/technical needs.
• Design and Implement an organization and DSCS wide GenAI / Agentic AI Framework strategy.
• Build, mentor, and lead a high-performing team; create a culture of continuous improvement, innovation, and enable solutions that enable data-driven decision making.
• Translate complex business needs into data-driven solutions; ensure BI solutions support strategic decision-making and operational excellence.
• Develop and Implement strategy for GxP Usage of AI Solutions, partnering with Global Development Quality and stakeholders in Digital Manufacturing Division.

Director, Agentic Business Intelligence Lead

Clinical Research

• Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications.
• Providing clinical development support of business development assessments of external opportunities to grow the Immunology Pipeline
• Developing clinical development strategies for investigational drugs and planning clinical trials (design, operational plans, settings) based on these clinical development strategies.
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational drugs.
• Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and Participation in internal and joint internal/external research project teams relevant to the development of new compounds.

Senior Principal Scientist, Clinical Research, Immunology

Director

• Supports execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and regions.
• Serves as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, Commercial, Publications).
• Contributes to the development of a single global scientific communications platform.
• Consolidates actionable medical insights from countries and regions.
• Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about Our Company’s emerging science.
• Organizes global expert input events (advisory boards and expert input forums) to answer Our Company’s questions about how to develop and implement new medicines or vaccines.
• Aligns plans and activities with Global Human Health (commercial) executive directors.
• Organizes global symposia and educational meetings.
• Supports key countries with the development of local data generation study concepts and protocols.
• Reviews Investigator-Initiated Study proposals from key countries prior to headquarters submission (ex-USA).
• Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company medicines or vaccines.

Senior Global Director, Medical Affairs – Dermatology

Software Engineer

• Deliver robust DS strategies for successful commercialization
• Provide technical oversight of cell culture process development, process characterization and regulatory filing activities
• Support DS commercialization, process characterization, control strategy development, tech transfer to internal and external manufacturing sites, process validation, second generation process development and health authority licensure
• Collaborate with colleagues across the US and internationally to elevate standards in biologics commercialization and manufacturing
• Champion compliance and safety; promote a culture of diversity, inclusion, and equity
• Mentor a team of scientists specializing in biologics commercialization, serving as the scientific/technical mentor for junior staff

Senior Scientist, Engineering

Medical Director

• Engage and train internal employees to ensure they comprehend the science behind the medicine
• Develop ongoing professional relationships with healthcare decision makers within a regional territory
• Provide accurate information across the full company product portfolio, clinical science, and quality management
• Collaborate and coordinate with other Medical Affairs colleagues to bring relevant health care solutions
• Serve as a resource for the USMA management team on health systems within territory
• Leads medical account management and planning with associated medical affairs functions for regional accounts and markets
• Maintain a macro view of the account to appropriately allocate company resources
• Build and develop breath and depth of relationships with key decision makers

Regional Health Systems Medical Affairs Director – TN, MS, LA

• Drives execution of the annual V&I plan with medical affairs colleagues from key countries and regions with a focus on the U.S.
• Acts as an empowered partner, making informed decisions with a strategic and agile mindset.
• Serves as the SME and connector across assigned therapeutic areas, translating global scientific platforms into actionable Medical Value Narratives (MVNs).
• Actively engages with country-level stakeholders—including medical advisors, payers, and scientific leaders—to ensure strategic alignment and support local data generation, congress planning, and advisory boards.
• Serves as the medical representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and Label), leveraging the V&I GMSA vision to drive strategic planning, outcome delivery, and tactical execution.
• Communicates pertinent information to stakeholders to inform and influence country and regional planning.
• Acts as the subject-matter expert, collaborating closely with V&I Outcomes Research (VIOR), Policy, Commercial, and Market Access teams to identify and address opportunities and barriers in key countries.
• Serves as a strategic partner for Big Country Markets (U.S., China, Japan) with no RDMA role.
• Plays a pivotal role in bridging global strategy with local execution, including understanding the needs of the U.S. Market.
• Consolidates actionable medical insights from countries and regions.
• Engages with a network of international scientific leaders and other key stakeholders about our company’s emerging science.
• Monitors external changing environment in partnership with the competitive intelligence (CI) team.
• Organizes global expert-input events to answer our company’s questions about how to develop and implement new medicines or vaccines.

Global Director – Medical Affairs, Atherosclerosis

Mechanical Engineer

• demonstrates working knowledge of combination product devices
• experienced in the design, development, and performance testing of secondary packaging for combination products with demonstrated experience operating packaging CAD programs (Solidworks and Artios) to design machinable, sustainable packaging solutions with deliverable solutions which perform in distribution testing
• designs, prototypes, conducts testing and analyzes data to inform design development activities
• has experience in design verification specifically focused on package distribution testing for combination products
• can specify standards for packaging materials not limited to paperboard and corrugate as well as packaging equipment for label application, carton and blister forming
• can generate drawings and specifications (design outputs) to be captured in Design History File
• collaborate with systems engineering team to develop robust set of design input requirements based on user needs and target product profile
• apply DFM/DFA principles to interrogate sourced device and packaging components or design bespoke device or packaging components
• develop test plans to understand design space and to ensure device and packaging technology is adequately suited for the combination product
• conduct or analyze tolerance stack ups utilizing worst-case and statistical methods such as RSS or Monte-Carlo simulation
• identify critical to function/safety and critical to process dimensions and ensure adequate controls exist to maintain device performance within acceptable range
• interface with key stakeholders in cross-functional development teams and provide technical insight and leadership on the device design aspects of the development program
• travel to OEMs/Suppliers to review product design, functional data, manufacturing processes and conduct due diligence on robustness of their product and process
• author design/ process FMEA to capture design related risks and identify appropriate risk controls to ensure robust and efficient device functionality
• author protocols, reports, create drawings and specifications to ensure proper documentation of development activities in accordance with relevant SOPs
• stay current with new device technologies, relevant worldwide regulations, standards, and effectively share this knowledge with others
• understand Process validation activities like IQ, OQ, PPQ etc.
• review and approve Process validation documentation

Device and Clinical Package Design Engineer

Artificial Intelligence

• 在指定的区域内, 达到指定产品的目标业绩,市场占有率和增长率,并有效地利用资源和控制费用
• 制定相应医疗机构的拜访计划并实施
• 向医疗机构提供医疗咨讯并介绍产品,使其了解并接受产品之特性和利益
• 挖掘现有市场潜力,并不断开发潜在市场,确保公司产品市场占有率的增长
• 执行公司市场开发策略和计划,完成新产品的进药计划
• 根据公司的推广策略组织有特色的学术活动推广产品

Senior Pharmaceutical Info Specialist, AI

Supply Chain

• Analyze large, multi-source datasets (ERP, APS, TMS, WMS) to identify trends, risks, and performance improvement opportunities
• Develop statistical models and analytics to support service levels, safety stock, forecast accuracy, lead time variability and inventory optimization
• Design and maintain dashboards and reporting tools that support daily execution and strategic supply chain decisions
• Establish, standardize and monitor global supply chain focused KPIs (e.g., OTIF, inventory turns, working capital, forecast accuracy)
• Leverage SAP expertise to align analytical outputs with planning parameters and system execution
• Partner with stakeholders to translate business challenges into structured analytical requirements and scalable solutions
• Present insights clearly to senior leaders and operational teams to enable confident, data-driven decisions
• Support digital supply chain initiatives by integrating analytics into APS, TMS, and WMS platforms
• Drive continuous improvement within a regulated, manufacturing-focused environment

Senior Specialist, Supply Chain Management Data – Analytics

Learning and Development

• Lead a global, multidisciplinary team responsible for end-to-end learning experience creation in support of an assigned Therapeutic Area (TA) and/or Commercial Capability portfolio.
• Conduct learning analysis, develop learning blueprints, and oversee creation of learning assets at global scale.
• Translate business and capability needs into innovative, scalable, and compliant learning solutions that drive performance, accelerate talent development, and support strategic priorities.
• Deliver learner‑centric, science‑based, inclusive learning experiences that meet our company's quality standards and produce measurable business impact.
• Partner with business stakeholders and GLD colleagues to analyze performance needs, identify skill gaps, and define clear learning and success outcomes.
• Ensure adherence to formal legal and medical review processes for compliant delivery of learning.
• Create and maintain high‑level designs and learning journeys for assigned portfolios.
• Lead and coach a global team of designers, developers, and vendors in a matrixed environment.
• Provide creative and quality oversight across all learning formats, reviewing designs and final deliverables.
• Serve as a trusted partner to business and GLD stakeholders throughout delivery.

Learning Creation Lead, Associate Director – Global Learning and Development

Content Marketing Manager

• Develops and adapts the Value & Implementation Planning & Scientific Platform for GSVC Annual Product and Disease State Plans
• Authors or works with vendors to create GSVC content aligned with Annual GSVC Plans, ensuring scientific accuracy and consistency
• Reviews and communicates GSVC content, integrating feedback from stakeholders
• Implements GSVC Plans, including medical information letters (MILs), verbal response documents (VRDs), slide decks, digital and modular content, innovative formats, and global congress medical booth materials, including staffing these booths
• Leads product- or disease area-related projects and initiatives, providing solutions for complex problems and mentoring junior staff
• Collaborates with global stakeholders to ensure assets align with strategic medical plans and meet customer and internal needs
• Identifies gaps and leads initiatives such as creating departmental processes, standard operating procedures (SOPs), and cross-functional activities
• Builds collaborative relationships across divisions and regions
• Drives alignment of scientific content strategy and plans with other V&I partners, such as Publications, Clinical and Outcomes Research
• Aims to ensure the timely availability of effective and compliant resources for Medical Information and Field Medical teams
• Provides training to internal stakeholders on GSVC-developed disease and product content

Global Scientific and Value Content Associate Director – Oncology, Breast and Gynecologic Malignancies

Customer Support

• reports to the Associate Vice President of US Marketing Operations in Commercial Excellence & Innovation
• leads the overall US Customer Service Center organization with accountability to direct the strategy and execution of engagements with Healthcare Professionals, Patients, Consumers, and Employees across five contact centers
• sets the vision, strategy, and governance for a critical service organization that supports Healthcare Professionals, consumers, patients, and employees
• directs a complex, multi-layered organization of approximately 80 Full Time Employees
• modernizes service centers through automation, advanced analytics, digital self-service, and AI-enabled customer engagement
• owns the design, governance, and performance of the CSC’s technology and AI-enabled service ecosystem

Executive Director, Customer Service Center Strategy – Ops Leader

• Lead and act as the primary interface on technical issues between technical operations and external partner
• Provide technical leadership within technical operations group for commercialization and manufacture of drug substance
• Provides technical guidance to external partner, assesses viability of technology in proposed process configurations
• Collaborates with external manufacturing operations, external quality, regulatory, to evaluate external partner performances
• Executes technical due diligence assessments at external partner
• Ensures tech transfers are positioned for successful business outcomes
• Executes validation strategies for new and existing products
• Provides manufacturing process support to external partners to resolve production issues
• Supports/coordinates/manages complex investigations
• Drives and supports continuous process verification and process performance monitoring program
• Understands the true regulatory requirements and partners with operations, quality, to develop more efficient ways to meet these requirements.

Associate Director – External Manufacturing

Marketing

• Strategic partner and Content Expert to Global Brand Team, ensuring strategy realization during launch lifecycle
• Leads core content creative execution efforts from briefing creation (Workfront), content development and management (tools/technology enhancements), Medical Legal Review (PRT) and compliant content accessibility & storage (DAM)
• Embraces and implements technology advances to drive further content creation efficiency
• Co-manage and provide oversight in day-to-day agency relationships specific to core content creation (timelines, consolidated direction, scope support)
• Partner with CA Agency Team for AOR escalations
• Consultative partner to development of Branding & Campaign Implementation Guidance ensuring brand consistency and standardization (supporting scalability)
• Collaborates to ensure ELMs/HHI have access to globally developed core strategic content, tools and technology for seamless re-use; executes governance plans
• Identifies and creates content to support Global Congress efforts for launch lifecycle, sharing recommendations with GHQ marketing stakeholders
• Manages content lifecycle during launch/post-launch period (global content renewals, updates, retirement)
• Model the Content Accelerator vision through rapid adoption of AI enhancements
• Consultant to Global Brand and Content Accelerator Teams providing input, guidance, updates and validation to operating model principles and structure

MSD