Software Engineer

• Oversee facility start-up /readiness for FLEx2 (GES capital project) and the daily operation of FLEx1 (facility in operation).
• This includes equipment engineering, automation, bio-sterile validation, maintenance & calibration, safety and compliance requirements to support development or GMP activities
• Oversee engineering activity and support for the Sterile Liquids Pilot Plant (WP17 SLP)
• Manage, develop, and grow a team of facility-facing engineers
• Provide trouble-shooting support on the shop floor
• Support internal capability development by evaluating and deploying innovative sterile manufacturing technologies to support new product development, both automated and non-automated
• Collaborate effectively within and across functional areas and possess advanced knowledge or experience in specialized engineering areas.
• Develop and lead Commissioning, Qualification & Validation activities (CQV)
• Participate in external and internal audits, tours, and inspections
• Ensure closure of investigations, as needed
• Establish and manage expense and capital projects, including expenditures via financial budgets and forecasts associated with the FLEx Center and the SLP
• Maintain facility and equipment systems in a state of permanent inspection readiness
• Recruit and develop staff, through objective setting, rewards and recognition, stretch leadership and/or technical assignments, and learning opportunities that broaden experience
• Sponsor and drive a culture of continuous improvement across these facilities

Director, Sterile Engineering

• Lead the development, maintenance, and assignment of training curricula, ensuring content remains current, relevant, and aligned with compliance requirements.
• Monitor, track, and report on training completion, effectiveness, and adoption of training technologies, supporting continuous improvement.
• Monitor the facility's environmental monitoring (EM) program, including data review, investigations, and execution of risk assessments to maintain compliance.
• Support inspection readiness and participate in internal and external audits, including GMP compliance audits and Safety/GMP walkthroughs.
• Review and assess evolving Quality Management System (QMS) documentation and procedures, assessing facility alignment with regulatory and internal requirements.
• Manage SOP governance, including periodic reviews and updates driven by quality or operational changes.
• Provide oversight for departmental investigations and change controls, ensuring timely closure, robust root‑cause analysis, effective action plans and CAPAs, and trend monitoring.
• Oversight and further establishment of the facility Aseptic Observer Program, performing observations, data mining, CAPA development, and cross‑functional communication of results.
• Lead operational responsibilities for the PSIM program, including protocol authorship, execution and planning oversight, management of annual qualifications, and support for sterility investigations.
• Drive skills development initiatives, including onboarding strategies, COE/consortium participation, and establishment and maintenance of competency and improvement trackers.
• Collaborate with Production, QA, and cross-functional teams to support compliance initiatives, continuous improvement efforts, and evaluation of new technologies.

Associate Director, Engineering

Data Analyst

• Develop techniques for quantitative analysis of multidimensional images
• Identify biomarkers in biological datasets
• Apply machine learning, deep learning, data mining, image processing, and signal processing techniques

Image Data Analytics Intern

DevOps Engineer

• Design, implement, and maintain IaC solutions using Terraform, Bicep, or ARM templates in Azure, with GitHub Actions for CI/CD pipelines and automated production deployments.
• Collaborate with security and infrastructure SMEs to integrate tools like Microsoft Sentinel, ADX, and Cribl into IaC workflows, ensuring seamless telemetry and analytics.
• Automate integrations across Azure services (e.g., Logic Apps, Event Hubs, Functions, Key Vault) to build resilient, scalable systems.
• Develop and deploy automated pipelines for data ingestion, monitoring, and compliance, partnering with teams to meet enterprise standards.
• Conduct code reviews, performance tuning, and cost optimization, iterating based on SME input to refine and deploy updates to production.
• Implement observability and monitoring practices (e.g., using Azure Monitor or Prometheus) to ensure system reliability and quick issue resolution.
• Mentor junior engineers and advise on IaC best practices, fostering a collaborative DevOps culture.
• Work in agile teams with incident response, threat hunting, and cloud engineering groups to translate requirements into deployable solutions.
• Ensure all deployments adhere to regulatory compliance (e.g., HIPAA, GDPR) in a biopharma context.

Senior DevOps Engineer

Marketing

• Support development of commercial data and insights for Global Vaccines portfolio priorities
• Conceptualize set of analytics capabilities and tools anchored to our marketing and launch frameworks to support decision making for Global Vaccines portfolio and assets
• Partner with global marketing teams, DHH teams, and other cross-functional teams to help inform strategic decisions and increase commercial rigor through all phases of pipeline asset development
• Serve as the Insights & Analytics quarterback to address key business questions through digital, data and analytics capabilities
• Understand and assist Strategic Portfolio Reviews, Trimester Business Reviews (QBRs), Prioritization meetings, etc.
• Synthesize & document key trade-off decisions and DHH aspirations for executive audiences via active updates to ongoing inventory of projects/initiatives (Book of Work)
• Analytics projects delivery with expertise in data manipulation, analysis, and visualization using tools such as Excel-VBA, PowerBI or similar technologies and capabilities

Specialist, Vaccines Global Marketing Engagement

Account Executive

• Engage with customers to address identified needs
• Educate key stakeholders about our oncology products
• Communicate with the broader oncology community
• Achieve or exceed assigned sales goals within the territory
• Work collaboratively with team members to ensure customers have a seamless experience
• Analyze and identify trends in a complex buying environment and develop strategies accordingly

Oncology Sales Representative

Clinical Operations

• Responsible for specific clinical/scientific activities on a single study or across multi e studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials).
• Support development of Protocol and related study materials (e.g., ICF documents/amendments, data management deliverables).
• May interact with internal and external stakeholders (e.g., country operations, committees, vendors) in support of clinical study objectives.
• Support development of site and CRA training materials
• Prepare clinical narratives
• Collaborate cross-functionally to monitor clinical study data to ensure quality, completeness, and integrity of trial conduct.
• Participate in CRF design to ensures data collection is in alignment with the protocol.

Scientist, Clinical Operations

Research Scientist

• Work with the Associate Vice President Immunology Discovery SD Research & Development Division and other project leads on site as well as other Research & Development Division Immunology Discovery sites to define and execute drug discovery immunology programs in the portfolio as part of the Immunology TA strategy
• Closely collaborate with a cross-functional group of experts across Our Company to design and execute the Research Operating Plan to advance projects through Discovery
• Lead the discovery and creation of cellular, molecular and functional assays required for design and execution of the Research Operating Plan to advance projects through Discovery and toward early development
• Partner closely with cross functional colleagues, including Computational Scientists (DAGS), modelers, PKPD, to advance projects forward through stages of Discovery
• Lead the discovery and creation of cellular, molecular and functional assays that serve as biomarkers for prosecution of programs as they advance through the Discovery stages toward Early Development
• Contribute to discovery and creation of translational data strategy for immunology including partnering internally and externally in the generation of actionable science packages to identify, validate and execute novel targets implicated in the pathogenesis of TA disease areas including diseases in the Derm, Rheum and GI areas
• Collaborate with Translational Medicine and Biomarker colleagues for programs moving toward Early Development to ensure transition of early discovery biomarkers and biomarkers plans for execution during development stages
• Champion the use of new technologies and modalities to drive discovery and prosecution of novel targets in immunological disease through various modalities and approaches including small molecules, peptides, biologics, T cell engagers and others
• Actively contribute to the overall company's Immunology TA strategy
• Maintaining awareness of scientific developments within area of expertise, in terms of new scientific findings, research methodologies, novel platforms and modalities
• Attend appropriate scientific meetings to maintain cutting edge knowledge and competency in the field

Senior Principal Scientist, Discovery and Translational Immunology

• Under the guidance of the Executive Director/Associate VP, Value & Implementation Outcomes Research, develop integrated evidence strategies for cardiometabolic products
• Plan and implement Outcomes Research and Real World evidence programs
• Represent V&I Outcomes Research on one or more Value Teams
• Critically assess drivers and barriers to reimbursement
• Develop the integrated evidence strategy including HTA/OR strategy
• Develop and evaluate health programs that enhance value and use of company products
• Generate value evidence deliverables, including global value dossier and health economic evaluations
• Collaborate with various teams and departments to communicate Outcomes Research findings

Principal Scientist – Outcomes Research, Cardiometabolic

• Lead development of commercial data and insights for Global Vaccines portfolio priorities
• Conceptualize set of analytics capabilities and tools anchored to our marketing and launch frameworks to support decision making for Global Vaccines portfolio and assets
• Partner with global marketing teams, DHH teams, and other cross-functional teams to drive strategic decisions and increase commercial rigor through all phases of pipeline asset development
• Serve as the Insights & Analytics quarterback to address key business questions through digital, data and analytics capabilities
• Lead Strategic Portfolio Reviews, Trimester Business Reviews (QBRs), Prioritization meetings, etc.
• Proactively manage projects delivery with expertise in data manipulation, analysis, and visualization using tools such as Excel-VBA, PowerBI or similar technologies and capabilities
• Leverage a variety of patient modeling techniques including statistical, patient-flow, and simulations-based techniques for insight generation.

Associate Director, Vaccines Global Marketing Engagement

• Provide regulatory leadership, oversight, and strategy to a team of Regulatory CMC Professionals in developing global Regulatory CMC strategy and executing submissions related to small molecule, development products.
• Lead oversight of multiple programs in Respiratory franchise and some conventional small molecule programs.
• Prepare applicable IND/CTA’s, Agency Background Packages, Worldwide Marketing Applications, and transfer strategy to post-approval group for further submissions occurring within several years post-launch in the major markets.
• Support a project in a similar capacity by providing direction to the team members that are responsible for developing and overseeing implementation of regulatory strategies.
• Assess CMC changes during development, defining regulatory requirements, developing CMC regulatory strategies, ensuring high quality, accuracy, and high likelihood of approval of all regulatory submissions.
• Develop, execute & provide oversight of regulatory initiatives & strategies of significant complexity.

Principal Scientist – Regulatory Affairs, CMC

• Responsible for developing and implementing CMC regulatory strategies for pharmaceutical pipeline products
• Serve as a CMC Product Lead for assigned products
• Lead development and execution of global product and project regulatory strategy(ices)
• Manage execution of CMC documentation including IND/CTA, original NDA/MAA
• Prepare and communicate CMC Risk Assessments, contingency plans, lessons learned, and escalate potential regulatory issues to management
• Partner with quality colleagues to prepare for and support pre-approval and regulatory inspections

Associate Principal Scientist, Regulatory Affairs – CMC

Clinical Research

• Planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area
• Evaluating pre-clinical and translational work for generating early clinical development plans
• Developing clinical development strategies for investigational or marketed drugs in Endometrial Cancer
• Planning and designing clinical trials
• Medical oversight and conduct of ongoing or new clinical trials
• Analyzing and summarizing clinical findings from studies
• Participating in internal and joint internal/external research project teams
• Supporting business development assessments

Senior Principal Scientist, Clinical Research – Endometrial Cancer

• This position drives scientific planning, strategy and execution of Phase 1-4 clinical studies
• Under the direction of the Program Lead, you will collaborate with global, cross­ functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.
• Responsible for the clinical/scientific execution of clinical protocol(s)
• Serves as the lead clinical scientist on the clinical trial team
• Collaborates with the Medical Writer on clinical/scientific and regulatory documents
• Partners with Study Manager on study deliverables
• Participates in the set up and design during study start up (e.g., database set up)
• Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director
• Builds talent and capabilities of direct/indirect team members through proactive coaching, mentoring and development opportunities
• May include management of direct reports including assignment of resources, professional development, and performance management.
• May serve as a subject matter expert and/or participate on process improvement teams.

Associate Principal Scientist, Clinical Operations – Immunology

Manager

• contribute to the operational planning and execution of one or more clinical trials
• develop leadership and technical skills as part of a global, cross-functional team
• apply project management, communication, and collaboration skills in support of our clinical trials
• have specific operational responsibilities for a single study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, etc.)
• responsible for tracking study timelines using project management tools
• share technical expertise with team members
• interact with internal and external stakeholders (e.g., study team, vendors, committees) in support of clinical trial objectives

MSD