Full-stack Engineer

• Lead the technical strategy, architecture, and design for the collar
• Translate customer and business needs into practical technical solutions
• Ensure the collar meets requirements for performance, reliability, manufacturability, and cost
• Work cross-functionally to support product discovery, experimentation, and field learning
• Define and oversee validation, quality, and launch readiness activities
• Identify and manage technical and production risks early
• Support field issue investigations and drive continuous improvement
• Track technical metrics and use data to guide engineering decisions

Lead Collar Tech

Research Scientist

• Participate in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical drug substance processes
• Conduct laboratory-scale and manufacturing-scale studies to support commercial process validation and characterization
• Design experiments, analyze data, and mentor junior staff, ensuring excellence in execution
• Provide technical leadership in interpreting trends from commercial process monitoring, driving further investigations and process improvements
• Actively interact with internal and external partners, representing your functional area on cross-functional teams to foster collaboration and innovation
• Author regulatory and technical documentation, ensuring all processes align with our company’s expectations
• Manage a small team of junior staff, guiding them in their professional development

Associate Principal Scientist, Biologics Drug Substance Commercialization – Associate Director

Director

• Leading a team of up to 7 QP2 scientists including people management, scientific and operational oversight, under the direction of the Therapeutic Area Head of Immunology
• Leveraging end-to-end drug discovery/development and disease area expertise to independently provide day-to-day scientific oversight to individual contributors
• Maintaining a comprehensive understanding of global regulatory expectations for all relevant modalities, shaping the clinical pharmacology regulatory strategy for selected immunology assets, and ensuring high quality regulatory documents (INDs, CSRs, CTDs)
• Applies immunology knowledge and strategic thinking to identify, prioritize and develop enabling modeling platforms (disease, mechanistic, comparator models) at scale to create a differentiated immunology portfolio in an end-to-end manner in partnership with key internal/external collaborators
• Implements quantitative clinical pharmacology, pharmacometrics and translational modeling efforts to streamline drug discovery and development strategies and integrating knowledge to inform key decisions
• Engaging as an expert representative for QP2 in cross-functional and governance discussions, including business development and licensing evaluations
• Setting priorities for direct reports and driving performance management, hiring and retention, staff development and training, and input into calibration and talent management processes
• In partnership with the Therapeutic Area Head of Immunology, identify resource needs and contribute to resource allocation internally
• Fostering a culture of collaborative and high-performing teaming

Executive Director, Quantitative Pharmacology, Pharmacometrics

Operations

• Manage the technical interface between our Company and External Partners (EP)
• Provide process support to External Partners for existing supply products to resolve production issues
• Evaluate and manage process change requests
• Proactively assess, and manage process/technical risks
• Provide guidance on process improvement and capacity optimization
• Provide oversight of External Partners during New Product Introductions and Technical Transfers
• Proactively identify process/technical risks as part of pre-execution activities
• Provide on-site support during execution
• Support post-execution activities
• Foster proactive partnerships with External Partners to meet business goals, identify and mitigate risks, and continuously enhance performance
• Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence.

Associate Director, Chemical Technical Operations

• Contribute to the creation and maintenance of access strategies, including:
• Value messaging
• Evidence generation
• Customer-facing resource development
• Contracting options across segments, including value-based approaches
• Distribution & specialty pharmacy
• Organized customer segmentation & site-of-care
• Provider access & reimbursement
• Patient access & affordability
• Impact of federal and state legislative policy
• Collaborate closely with internal stakeholders (account leads, medical affairs, brand marketing, global marketing & access teams, pricing, regulatory, compliance, legal, etc.) and external partners (agencies, etc.) to aid in the development of US market access strategy
• Create and implement innovative marketing materials to support engagement with organized customers and formulary decision makers at launch and throughout Intismeran’s life cycle
• In collaboration with cross-functional stakeholders, develop internal materials and trainings to ensure launch readiness, including any future operational changes and new indications
• Partner cross-functionally with US and global teams (Access, Marketing, Finance, Regulatory, and V&I Outcomes Research) to identify evidence gaps and align on access opportunities, evidence generation, and launch readiness.
• Aid in aligning finance inputs for annual and long-term forecasting of new products
• Build capabilities through the creation and maintenance of modeling, research, dashboards, and analysis supporting early product access

Associate Director, US Oncology Market Access – New Product

QA Engineer

• Oversee the end‑to‑end quality program for an assigned product value chain in antibody drug conjugates.
• Be a core member of the Value Chain Management Team, partnering across functions to ensure a reliable supply of high‑quality products throughout their commercial lifecycle.
• Lead end‑to‑end quality oversight for the product program, ensuring compliance with procedures and regulations.
• Develop and maintain the Product Quality Strategy and Product Analytical Strategy in line with supply strategy.
• Partner with Quality, Regulatory, Technical, Supply Chain, and site Quality teams to align priorities and resolve issues.
• Strengthen and harmonize Quality Management Systems and ways of working, sharing best practices across sites.
• Stay current with regulatory requirements, support or lead inspections, and drive ongoing inspection readiness.
• Provide quality leadership to product focus teams, the Value Chain Management Team, and related working groups.
• Lead quality communications across the network, including meetings, updates, and escalation of issues and risks.
• Support analytical siting strategies and broader value‑chain projects, ensuring quality input and follow‑through.
• Track and interpret change control, complaints, and quality performance data to identify trends.
• Review Annual Product Reviews, evaluations, and post‑marketing product reviews to assess and communicate risks.
• Monitor, report and mitigate quality and supply chain risks across the franchise.

Director, Quality Assurance – Value Chain Management

• Dispute resolution with appropriate escalation
• Balancing our company's delivery requirements with contract manufacturer’s production plan.
• Materials Management (ERP transactions, Logistics)
• Oversight of shop floor production (determining when an ExM functional rep should be deployed to the contract manufacturer’s facility)
• Continuous Improvement activities
• Partners with Procurement in the Identification/Selection of new contract manufacturers and Negotiation/Termination of Supply Agreements, as required
• Facilitates the collection of contract manufacturer’s capacity information (e.g. stated capacity, firm capacity, future capacity plans, time horizon/lead times required, comments/concerns, etc.), presents the information to Supply Chain Management and drives recommendations for capacity expansion at contract manufacturers, as required
• Ensuring alignment of the Supply and Quality agreements
• Executing ERP transactions associated with receipt and movement of company owned inventory, book-to-physical reconciling of company owned inventory at contract manufacturers, and documenting and witnessing destruction of company owned inventory
• Ensuring contract terms agreed upon by our company and the contract manufacturer including, but not limited to, purchase orders, forecasts, deliveries, and invoice payments are executed in compliance with the Supply Agreement
• Partners with the ExM Company Production System experts and other functionalities supporting ExM (e.g. technical, quality, procurement, etc.) to identify continuous improvement opportunities at contract manufacturers and supports Project management support to the DP NA regional team, and to ensure a greater coordination of ongoing projects within the region

Associate Director – External Manufacturing

• Design, develop, and maintain integrations with Veeva Vault Clinical using Veeva APIs (REST), Vault Loader, connectors, and MuleSoft (Anypoint Platform)
• Build and optimize data ingestion/extraction workflows (bulk loads, document transfers, metadata updates) using Vault Loader and automation scripts
• Create and execute API test suites in Postman; define collections, tests, environment variables, and automation to validate endpoints and workflows
• Produce complex reports and dashboards across Vault CTMS, including data modeling and transformations
• Collaborate with business stakeholders to translate requirements into technical solutions aligned to the Vault Clinical object model
• Manage releases across environments (DEV/VAL/PROD), including:
• o Configuration changes (lifecycles, workflows, object fields, roles/permissions)
• o SDLC adherence (requirements, design, code/config, testing, approvals, deployment)
• o Change control, versioning, and validation documentation (traceability, test evidence)
• Use JIRA for work management: create/maintain epics, stories, tasks; define acceptance criteria; manage sprints; track defects and release notes
• Implement operational monitoring and alerting; perform L2/L3 support and root-cause analysis for integrations, connectors, and reporting pipelines
• Maintain technical documentation (solution designs, mappings, API guides, job aids) and contribute to continuous improvement of engineering practices

Senior Software Engineering Specialist, Veeva Specialist

Account Executive

• Drive meaningful patient impact by leveraging scientific expertise and serving as the primary contact for customers within your assigned territory.
• Collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions.
• Develop and execute a territory-level business plan in alignment with company policies, standards, and ethics.
• Maintain current product knowledge and certifications for the company’s portfolio.
• Conduct balanced and compliant product sales discussions with health care providers and business professionals to align customer needs with company products according to product labeling.

Chronic Care Specialty Sales Representative

Compliance

• Supports products in the Oncology therapeutic area as part of a regulatory team
• Work closely with a global regulatory lead(s) to help develop and implement a global strategy for registration and/or maintenance of products
• Assisting in Regulatory Agency communications and submissions, including marketing applications, investigational new drug (IND) applications, pediatric plans and annual or other periodic reports
• Implementing strategy to develop Agency background packages and documents associated with regulatory submissions for marketing applications
• Communicating with Agencies and attending Agency meetings as needed
• Participating as an active member on the global regulatory team
• Conducting research and review of guidelines, regulatory precedence and competitive intelligence to facilitate development of regulatory strategy
• Assisting with process improvement initiative
• Performing regulatory administrative activities, as needed

Associate Director, Regulatory Liaison – Oncology

DevOps Engineer

• Build relationships across the broader IT organization to increase adoption and maturity of SRE, Observability, and Resilience practices
• Define and evolve the strategic vision for enterprise reliability engineering and ensure alignment across product, platform, and ITSM teams
• Establish and enforce standards for Service Level Objectives, observability frameworks, and resilience engineering practices
• Collaborate with engineering teams to ensure reliability is embedded into architecture, design, and delivery processes
• Drive adoption of Service Level Objectives using Nobl9 as the system of record for reliability governance
• Lead evaluation and introduction of new technologies that improve reliability outcomes while integrating with existing platforms
• Apply AI capabilities to enhance reliability practices, including incident triage, diagnostics, and automation, in a governed and controlled manner
• Collaborate within efforts to standardize observability across logs, metrics, traces, and events to improve system visibility and decision-making
• Consult and promote resilience patterns including fault isolation, failover strategies, and recovery mechanisms
• Guide improvements surrounding incident lifecycle effectiveness, including detection, response, root cause analysis, and continuous improvement
• Lead and mentor a community of reliability practitioners to grow organizational capability and maturity
• Represent reliability engineering practice in architecture reviews, governance forums, and key IT initiatives
• Drive continuous improvement of reliability practices through research, innovation, and feedback from engineering teams

Senior Staff Reliability Engineer, Software Engineering

Medical Director

• planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area
• manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication
• Evaluating pre-clinical and translational work for generating early clinical development plans and Investigational New Drug applications
• Developing clinical development strategies for investigational or marketed RCC drugs
• Planning clinical trials based on the clinical development strategy
• Medical oversight and overall conduct of ongoing or new clinical trials for investigational or marketed drugs
• Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy
• Participating in internal and joint internal/external research project teams relevant to drug development
• Supporting business development assessments of external opportunities

Senior Clinical Director, Clinical Research

Clinical Research

• Managing and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group and in the field of Thoracic Oncology.
• Managing the entire cycle of clinical development, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meetings.
• Provide internal scientific leadership for cross-functional areas supporting clinical trials and interact externally with key opinion leaders.
• Evaluating pre-clinical and translational work for generating early clinical development plans and Investigational New Drug applications.
• Developing clinical development strategies for investigational or marketed agents that incorporate the latest scientific developments, regulatory requirements, competitive landscape, and commercial considerations.
• Planning clinical trials based on these strategies.
• Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed agents.
• Analyzing and summarizing clinical findings to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publications.
• Participation in internal and joint research project teams relevant to the development of new compounds and the further study of marketed compounds.

Distinguished Scientist, Clinical Research, Thoracic Malignancies

• Sets vision and strategy for cheminformatics capabilities and platforms that accelerate scientific learning and decision-making in drug discovery
• Leads a multi-site team of cheminformatics and data science specialists, spanning data engineering, analytics, and scientific software development
• Actively develops talent, fosters diversity of thought, and builds an inclusive culture that engages and empowers all team members
• Engages stakeholders across the drug discovery spectrum—from early target identification and chemical biology through lead optimization and safety—to understand needs and enable impactful solutions
• Translates scientific challenges into scalable data architectures, workflows, and algorithmic approaches that can be broadly leveraged across multiple projects
• Drives development of next-generation cheminformatics workflows through integration of modern technologies, including machine learning (e.g., generative and predictive modeling), knowledge graphs, and emerging AI approaches
• Ensures that developed capabilities are effectively deployed and adopted in collaboration with project teams and modeling partners
• Builds and maintains strong partnerships with IT to co-develop robust, sustainable platforms supporting scientific workflows
• Balances strategic investment in new capabilities with effective utilization of existing solutions to maximize organizational value
• Collaborates with leaders across Bioinformatics, Biostatistics, Quantitative Biology, and Modeling to align on data science strategy and priorities
• Contributes to cross-divisional alignment on the role of data science and informatics in the organization
• Works closely with Modeling, Structure, and Biophysics leadership to identify opportunities where cheminformatics can enhance broader modeling and discovery efforts
• Maintains visibility across the discovery portfolio to identify emerging needs and opportunities for scalable cheminformatics support

Director, Cheminformatics – Modeling & Informatics

• Collaborating with internal and external stakeholders across transportation, warehouse operations, supporting functions, and finance to ensure the timely payment of our Company’s freight invoices in accordance with contracts.
• Producing key financial reports and collaborating with regional and local finance to facilitate month-end close and accruals.
• Supporting global transportation budget overview and reporting to monitor and explain monthly performance against the plan.
• Ensuring accurate general ledger coding and cost allocation.
• Collaborating with division and corporate leadership to identify requirements and develop strategies for the development, implementation, and monitoring of freight audit and payment processes both within the region and globally.
• Ensuring compliance with internal accounting requirements including industry and legal requirements and standards.
• Measuring and reporting the effectiveness of the audit and payment processes.
• Ensuring the transfer of freight payment data from the audit and/or payment provider into our company’s system of record.
• Ensuring our company’s reporting system and the provider’s system are in balance.
• Determining metrics, implementing changes to drive business improvements, and maintaining dashboards to achieve targets and communicate progress monthly, quarterly, annually.
• Conducting regular process improvement reviews to identify automation or enhancement opportunities and managing those improvement projects to completion within the Fiscal Year Targets.
• Managing relationship and ongoing improvement projects with third-party freight audit providers.
• Mentoring and training team members and new hires on freight audit and payment policies, procedures, and system functionalities to foster a collaborative and knowledgeable team environment.

MSD