Director

• Translate business needs and priorities to build analytical plans that answer business questions by providing actionable insights.
• Effectively communicating advanced analytics to stakeholders to inform business decisions.
• Communicate & collaborate effectively with cross functional teams with competencies in market research, forecasting, commercial analytics, data science, customer engagement, data strategy, population health, competitive insights, marketing operations, medical & clinical backgrounds.
• Analyze data across disparate databases/sources (including claims/EMR Data and other sources) to develop insights that inform commercial business strategies.
• Stay current with industry trends and advancements in analytical methodologies to bring new ideas forward (including application of GenAI) that will enhance analytic capabilities of the organization.
• Contribute to innovative experiments, specifically to idea generation, idea incubation and/or experimentation, identifying tangible and measurable criteria to make meaningful improvements to the business processes and strategies.
• Derive actionable business insights from various data sources, develop clear data story, and communicate effectively to business stakeholders.
• Lead and mentor a team of data scientists and business analysts (on-shore and off-shore), providing guidance on best practices in data analytics, modeling and data visualization, through the scope of a project.

Associate Director, Business Insights & Analytics, Immunology

• Develop and co-own with Digital Manufacturing a multi-year digital and data strategy for biologics late-stage pipeline and inline aligned with enterprise priorities; translate strategy into a prioritized execution roadmap with clear business cases and ROI metrics., and drive execution against that roadmap.
• Establish approach and drive acceleration of adoption of analytics, statistics, modeling, AI/ML and structured content practices in Bio S&T, while holding functions accountable for execution.
• This role will also be responsible for integrating across the Bio S&T functions in driving a robust knowledge management and document management strategy for CMC filings.
• This will be done in close integration and collaboration with Digital Manufacturing and Digital CMC.
• This role will oversee the integrated data architecture and governance model within Bio S&T that unifies process data across upstream/downstream, scale-up/tech transfer and commercial operations, including external CMOs/CDMOs.
• Serve as Bio S&T functional owner for key lab/process systems across Bio S&T (e.g ELN, utilization of VTN, KX etc); drive adoption and enable cross program learnings.
• Coordinate and sustain maintenance of process platforms and standards across Bio S&T functions, with functions holding content accountability.
• Identify needs, develop biologics tech business strategy for mechanistic/statistical modeling, predictive analytics, digital twins, and support NLP-enabled data extraction driving Bio S&T level execution of Digital CMC strategies, ensuring sustainability and efficiency.
• Drive strong collaboration with Digital Manufacturing to link business and data science & analytics capabilities in Digital Manufacturing.
• Define, track and report KPIs for data quality, model impact, process performance (yield, cycle time, first-pass success), submission timelines and cost savings, while driving execution through Bio S&T functions.
• Drive operationalization of analytics into workflows (experimental design, tech transfer, manufacturing control, lot release) and partner with continuous improvement teams to capture efficiencies.
• Integrate at site technology process data leads and above site process data leads driving to efficient and sustainable execution of overarching biologics data strategy and process monitoring.
• Oversee and streamline statistics support & training across Manufacturing process and analytical working groups, and functions.
• This role will partner very closely with Digital Manufacturing and Digital CMC to drive an integrated strategy for biologics across Bio S&T functions.
• This team will integrate existing local efforts on data management, data strategy, modeling, statistics, data sciences within Bio S&T.
• Drive change and adoption of data and digital mindset within Bio S&T across all functions and all levels of the organization.
• Recruit, develop and retain a multidisciplinary team; champion inclusive talent management and succession planning.

Executive Director, Bio S&T Platform, Data, Statistics & Modeling

Data Scientist

Associate Director, Business Insights, Analytics & Data Science, Ophthalmology

Operations

• Lead a team to manage a network of contract manufacturing organizations, ensuring achievement of KPIs around supply, compliance and cost.
• Lead the cross-functional team of Operations, Quality, Technology, Procurement, and Supply Chain to manage all aspects of supply.
• Develop and manage a forward-looking strategy for this CMO Platform.
• Develop a risk management process, continuously assess and mitigate supply and compliance risks.
• Responsible for all aspects of 3rd party risk – including EHS, bribery/corruption, labor, etc.
• Exhibit a high level of financial compliance and financial stewardship.
• Develop an industry-leading team of operations managers.
• Drive productivity and discard reduction.
• Drive improvements in service, lead time and productivity.
• Maintain GMP compliance across the network.
• Interface with CMO Business Leaders as needed to resolve issues and to create business opportunities.

Executive Director, Animal Health External Manufacturing Operations

• Assist with data collection, cleaning, preprocessing, and analysis from diverse biomedical and research sources.
• Contribute to the development, implementation, and validation of data models and analytics pipelines.
• Work collaboratively with data scientists, IT specialists, and research staff to analyze experimental results and generate actionable insights.
• Develop visualizations and dashboards to communicate findings to both technical and non-technical stakeholders.
• Document methods, code, and results following department and industry standards.
• Participate in team meetings, present work progress, and contribute to brainstorming sessions.

Data Science and Scientific Informatics Intern

Controller

• Track and report on program budgets, actuals, run rates, and KPIs
• Support financial governance and compliance with reporting standards
• Prepare financial dashboards and reports for leadership review
• Collaborate with PMO and program leads to manage financial risks and dependencies
• Ensure transparency and traceability of financial data across the program
• Assist in identifying cost optimization opportunities and efficiency strategies
• Maintain documentation and audit trails for financial transactions and decisions
• Contribute to continuous improvement of financial management processes
• Responsible for an in-depth understanding of the business case and set-up of budget to serve as baseline
• Partner closely with budget owners on the required budget tracking and establishing acceptable thresholds against baseline

Financial Controller

Research Scientist

• Provide statistical support and leadership for projects related to the evaluation of clinical safety data.
• Interact with cross-functional Risk Management Safety Teams (RMSTs) on planning and executing evaluations of safety data for clinical development programs.
• Design, develop and evaluate processes, methods and tools for safety data evaluation.
• Collaborate with Clinical Safety and Risk Management, Clinical Research, Early Development Statistics, Late Development Statistics, Epidemiology, Scientific Programming, and other groups, on drug/vaccine safety evaluation from the Investigational New Drug (IND) through New Drug Application (NDA) to post-marketing phases of development programs.
• Provide statistical support and leadership to cross-functional RMSTs for strategic planning and statistical analysis activities supporting safety evaluations.
• Collaborate on planning and executing aggregate safety evaluations for: clinical trials during a development program, regulatory documents (e.g., DSUR, IB), and responses to safety-related inquiries.
• Ensure that all deliverables meet analysis requirements, standard operating procedures, and regulatory requirements.
• Evaluate the appropriateness of available software for planned analyses and ascertain the need for development of novel statistical methods or programming.
• Design, develop and evaluate processes, methodology and tools for product safety evaluation to support ongoing aggregate safety data analysis.
• Prepare oral and written reports and presentations to effectively communicate safety analysis results to project teams, management, regulatory agencies, or individual investigators.
• Stay current regarding regulatory guidance and methods for the evaluation of safety data.
• Participate in research activities for innovative statistical methods and applications in clinical safety evaluation.

Associate Principal Scientist, Biostatistics, Clinical Safety Statistics

QA Engineer

• Oversee the end‑to‑end quality program for an assigned product value chain in antibody drug conjugates.
• Coach, influence and connect teams across the network, bringing clarity on quality expectations and helping others solve complex problems.
• 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.
• Track and interpret change control, complaints, and quality performance data to identify trends.

Director, Quality Assurance – Value Chain Management

Technical Product Manager

• Analyze business problems and translate requirements into actionable product backlog items and user stories
• Incorporate input from Business System Owner (BSO) and other stakeholders to ensure alignment with strategic goals
• Support product team to prioritize high-impact work and continuously reassess priorities as new insights and data become available
• Maintain and prioritize a healthy backlog of well-formed epics, features and user stories which align with the overall roadmap and serve as requirements for the delivery squad based on the objectives and Key results
• Partner with squad members including but not limited to scrum masters, technical lead(s) and development team in release planning to manage high-quality product delivery leveraging Agile and Digital SDLC methodology
• Conduct and/or participate in agile ceremonies (sprint planning, reviews, retrospectives)
• Collaborate with engineering and design to ensure work is well refined, scoped and ready for delivery; accept user stories before they enter sprints
• Provide an escalation point for delivery issues or deconflicting dependencies that affect multiple teams across products
• Capture dependencies for execution and focus on reducing impact
• Communicate product updates, progress, risks, and plans to stakeholders

Junior Technical Product Manager

• Provide Competitive Intelligence (CI) leadership by deeply understanding the external healthcare environment and our company's internal business
• Utilize business and competitive intelligence to provide unbiased and fact-based competitive insights, benchmarking, and recommendations for commercialization strategies, portfolio prioritization, clinical development/research strategies, and Business Development initiatives
• Partner with discovery and clinical colleagues to shape research programs
• Analyze select competitor activities through strategic assessments, such as market situation analysis, strategic forecasting, and operational benchmarking
• Monitor and benchmark strategic plans and insights into our company's competitors, providing early warning for potential threats and opportunities
• Maintain a comprehensive understanding of relevant healthcare environment matters, including policy, regulatory, and health technology
• Develop a global internal network of subject matter experts to share intelligence and support strategic activities
• Support the design and execution of competitive planning initiatives for products subject to significant competitive events
• Ensure the effective implementation and integrity of all competitive and business intelligence activities
• Apply ethical and legal standards to all competitive intelligence activities.

Atherosclerosis and Metabolic Disease Competitive Intelligence Director

• Lead all administrative and operational functions of the company's Research Laboratory Institutional Animal Care and Use Committee (IACUC) in South San Francisco
• Participate in the continued development, implementation and oversight of the post-approval monitoring program
• Support quality improvement activities to promote research integrity across all research sites
• Ensure that the research carried meets both statutory, regulatory, and company ethical obligations
• Provide day to day management and oversight of the animal use protocol review process using a web-based protocol tracking system for submission
• Interface with IACUC members and investigators
• Serve as the primary contact for the principal investigators for questions related to the protocol review process
• Act as a resource for investigators on issues relating to the regulatory requirements for the use of animals in research
• Plan and coordinate IACUC meetings
• Prepare the IACUC Meeting Agenda and accurately record IACUC Meeting actions
• Prepare semi-annual program reviews by the IACUC
• Conduct initial administrative and compliance review of all submitted protocols and amendments
• Use professional knowledge to assess completeness
• Assist investigators in preparation of animal procedure statements and/or responses to requests or revisions made the IACUC
• Maintain all protocol records, IACUC minutes, semi-annual program reviews, AAALAC program descriptions and correspondence
• Report results and findings of the facility inspections to the IACUC
• Prepare the semi-annual report for the Institutional Official
• Ensure that IACUC appointment letters are current for all required positions
• Discuss with laboratory and research staff to ensure that protocols and approved procedures are being followed and that research personnel performing the procedures have been appropriately trained and are approved by the IACUC to participate in research projects
• Review in-life procedures, records and other forms of documentation to further ensure that protocols and procedures are being conducted as approved in the IACUC protocols
• Report findings as well as recurrent, program-wide issues to the IACUC
• Support routine and/or ad hoc requests for data trending & metrics and analysis
• Plan, initiate, conduct and lead vendor assessments & audits
• Promptly report significant compliance issues to the Animal Welfare team and to the IACUC
• Ensure tracking and completion of audit findings and reports

Associate Director, Animal Welfare

Clinical Operations

• This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.
• Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s).
• Serving as the lead clinical scientist on the clinical trial team.
• Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director.
• Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments);
• Partners with the Study Manager on study deliverables.
• Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming.
• Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct.
• Providing tactical/scientific mentorship to other clinical scientists.

Senior Scientist, Clinical Operations – ID/Vaccines

• The intern work is mainly in the Corporate Aviation function for the Company.
• This includes working with the pilot and operations functions supporting the transport of key company's personnel in worldwide operations.
• Providing general administrative support.
• Collecting information and developing solutions to specific projects of a limited scope.
• Assignments may be designed to develop professional knowledge and to provide broad experience and familiarization with our Company's Aviation and our Company's methods, standards, procedures, and practices.

Aviation Operations Associate – Intern

• Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations.
• Coordinate and/or support the preparation of procedures, processes and quality improvements.
• Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times.
• Assists in the coordination of significant quality events including fact finding, investigation support
• Collaboration across IPT functional and business areas to ensure robust processing, continuous improvement and cross-functional team building.
• Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities.

Quality Assurance Specialist

Software Engineer

• The Sr. Facilities/Utilities Engineer is a member of the Plant Engineering team providing technical support to the Wilson Site
• This support position will focus on investigation of utility/facility system excursions, system improvements and optimizations.
• The incumbent will also be responsible for leading plant engineering improvement projects and implementation of productivity enhancement initiatives.
• Manages capital projects involving plant engineering equipment replacement/upgrades.
• Apply management skills to align work activities with department objectives.
• Participate in the identification and implementation of process improvement projects, productivity initiatives and corrective actions while focusing on equipment uptime, minimizing cost, and maintaining process consistency.

MSD