Data Analyst

• Lead the Operational Reporting & Insights function at an organizational level
• Shape strategy, drive adoption of advanced reporting technologies, and foster talent development
• Define and drive clinical/operational reporting strategy across products, roles, and geographies
• Lead the roadmap and governance for solution delivery, including requirements, data readiness, development, testing, release, and maintenance
• Establish portfolio-level trend, risk, and opportunity reporting with executive-ready narratives and visualizations
• Translate insights into portfolio priorities and experiments while framing assumptions, caveats, risks, and success criteria
• Implement intake and prioritization for ad hoc analytics and convert recurring requests into scalable self-service solutions
• Direct industry benchmarking and synthesize insights into performance targets and investment decisions
• Define and govern reporting metrics and standards; use adoption and value metrics to refine priorities
• Oversee enablement and change management support for solutions
• Align data refresh and source priorities with business needs; establish reliability KPIs and communication norms for changes and incidents
• Set principles for access policies, workspace structures, and permission models
• Build team capability through development standards, documentation standards, mentoring, and upskilling
• Create a continuous learning and innovation agenda and operationalize new technologies and reporting methods
• Set objectives, assign work, set priorities, conduct reviews, coach performance, and provide recognition
• Develop career plans, growth opportunities, promotion cases, training, and mentoring
• Lead recruiting and hiring and manage sensitive employee relations with HR
• Balance workloads, coordinate contingent resources across geographies, and ensure effective handoffs
• Manage the operating budget and optimize spend
• Align teams around direction and facilitate team/functional meetings
• Champion organizational change and adoption of new operating models and digital capabilities
• Support staff in resolving unique operational challenges through engagement, facilitation, mentoring, and expert problem-solving

Director, Digital Process & Data Analytics, Global Data Management and Standards

Clinical Research

• Plan and direct clinical research activities involving new or marketed medicines in the Cardiovascular and Respiratory therapeutic area
• Manage the clinical development cycle for assigned studies, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication
• Plan clinical trials and collaborate on operational plans based on clinical development strategy
• Provide medical oversight and manage conduct of ongoing or new clinical trials for investigational or marketed drugs
• Analyze and summarize clinical findings to support safety and efficacy decisions, new drug applications, clinical study reports, and publications
• Participate in internal and joint internal/external research project teams
• Support business development assessments of external opportunities
• Engage with other functional areas to support study execution
• Collaborate with commercialization, regulatory affairs, statistics, and manufacturing experts to manage clinical development projects
• Keep colleagues informed about study progress involving company and competitor drugs
• Provide expert opinions internally and externally on relevant scientific questions
• Maintain awareness of scientific developments and research methodologies
• Identify strong investigators and establish communications with prominent clinical investigators
• Attend scientific meetings to maintain competency and awareness of research activities
• Author development documents, presentations, budgets, and position papers
• Facilitate collaborations with external researchers around the world
• Travel on company business to manage future or ongoing clinical research projects

Director – Principal Scientist, Clinical Research, Respiratory

General

• Provide technical and program leadership for the lifecycle management of critical biomaterials used in animal health biologics production and testing
• Lead biomaterials knowledge management, including production history, characterization, inventory status, qualification status, and method dependencies
• Manage biomaterials inventory strategy, including reorder levels, usage trends, lead times, expiry risks, and replacement triggers
• Lead replacement biomaterials planning through outsourcing, commercial vendors, and internal sourcing options
• Design, coordinate, and document equivalence qualification studies for replacement biomaterials to support USDA approval
• Lead or support method remediation when biomaterial changes or performance issues impact biological test methods
• Coordinate transfer of biomaterials and remediated methods to QC laboratories
• Prepare technical reports, qualification summaries, scientific justifications, and regulatory support documents for USDA review
• Partner cross-functionally with Manufacturing, QC, QA, Regulatory Affairs, R&D, and external suppliers

Biomaterials Program Lead

Communications

• Lead strategic communications for all U.S. Human Health manufacturing sites
• Develop and execute communications strategies supporting site and network business objectives, employee engagement, change, and reputation
• Advise Site Leadership Teams and work with Plant Managers and cross-functional program leads
• Lead a team of four U.S. site communicators
• Lead sensitive communications involving workforce restructurings, environmental or safety incidents, and regulatory enforcement
• Coordinate with U.S. and Asia site communicators to align global communications and standardize best practices
• Lead end-to-end employee communications on strategy, performance, priorities, safety, quality, compliance, and inclusion
• Partner with HR, Operations, EHS, Quality, and communications/corporate affairs teams on change management, organizational design, and network transformations
• Coordinate external communications, media engagement, community and stakeholder relations, and major announcements
• Lead issues management and crisis communications, including localized plans, scenarios, messaging, and response coordination
• Support communications for regulatory inspections, approvals, capital projects, technology transfers, new product introductions, and other milestones
• Develop content including leader messages, intranet content, presentations, videos, talking points, and FAQs
• Build a community of practice for U.S. site communicators and partners
• Establish and track communications KPIs and provide insights and recommendations to leadership
• Co-lead executive visits and events at U.S. sites
• Manage external agencies, consultants, and vendors
• Coordinate with global Manufacturing Division communications colleagues
• Represent the Manufacturing Division on enterprise and product communications councils and teams
• Lead global communications for the External Manufacturing team

Director, Site Communications – Human Health Manufacturing

Operator

• Work directly on the production line by monitoring, supplying, and packaging products on the machines
• Ensure product quality standards and maintain an organized workstation in accordance with safety regulations
• Follow the company’s golden safety rules and safeguard your own safety and that of other employees
• Perform activities in accordance with the company’s safety and environmental procedures
• Supply raw materials and consumables and package finished products according to standard procedures
• Keep the workstation clean and organized in accordance with 5S and TPM programs
• Monitor and operate machines correctly, requesting maintenance when necessary
• Ensure accurate production reporting
• Share knowledge of activities when necessary
• Complete production forms according to the department’s standards
• Ensure product quality and perform process inspections
• Report and ensure production volumes, explaining any variances
• Perform rework and product inspections when necessary
• Implement improvement projects within the department
• Support other departments when requested
• Work the afternoon shift: Monday through Friday from 1:30 p.m. to 10:00 p.m. and Saturday from 9:00 a.m. to 1:00 p.m.

Production Operator I – Afternoon Shift

Compliance

• Implement CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance, and defined regulatory strategies
• Prepare and review information required for regulatory CMC dossiers for commercial products
• Provide input to global product and project regulatory strategies by assessing CMC changes and identifying global regulatory requirements
• Evaluate supporting documentation for acceptability and potential risks
• Lead development, authoring, and review of CMC submission components for post-approval supplements/variations, annual reports, registration renewals, and health authority responses
• Liaise with global CMC, Manufacturing, and external partners to support compliant change management
• Assess and communicate regulatory risks and propose mitigation strategies
• Deliver regulatory milestones across the product lifecycle
• Identify and communicate regulatory issues to GRACS CMC management as needed

Manager, Regulatory Affairs – CMC

Platform Engineer

• Lead engineering execution across the Veeva Platform ecosystem
• Translate platform engineering strategy into executable plans and measurable outcomes
• Manage and develop a multidisciplinary team of engineers and specialists
• Partner with Product Owners, Scrum Masters, business stakeholders, Vault teams, vendors, and matrix teams
• Drive adoption of reusable engineering standards, integration patterns, release practices, and configuration best practices
• Balance divisional requirements with scalable, secure, reusable enterprise platform objectives
• Provide technical leadership across Veeva Vault implementations, integrations, and platform services
• Lead security initiatives including MFA enablement, authentication modernization, OAuth adoption, and technical-risk remediation
• Manage vendors and matrix teams in a complex global environment
• Champion AI-enabled engineering practices, automation, and continuous improvement
• Build and operationalize a high-performing Veeva Platform Engineering delivery team
• Deliver strategic platform backlog initiatives and roadmap-aligned engineering commitments
• Optimize release management across the Veeva ecosystem
• Promote enterprise-first thinking and evolve the Veeva Platform into a scalable, secure, reusable enterprise capability

Associate Director, Veeva Platform Engineering Lead

Security Engineer

• Design, implement, and support HashiCorp Vault in on-premises environments
• Develop reusable patterns, standards, and onboarding guidance for HashiCorp Vault and secrets management
• Support HashiCorp Vault integrations with CI/CD platforms, deployment pipelines, automation workflows, and application delivery processes
• Enable secure injection, retrieval, rotation, and lifecycle management of secrets for build, release, and runtime environments
• Integrate privileged access management with enterprise applications, infrastructure, cloud platforms, and APIs
• Troubleshoot complex technical issues and support production operations
• Develop automation, standards, and operational processes that improve security, efficiency, and audit readiness
• Collaborate across identity, automation, cloud, infrastructure, and application teams

Senior Cybersecurity Engineering Specialist

Medical Director

• Lead business-facing digital and visual analytics and AI-driven initiatives modernizing clinical data review and medical monitoring
• Drive organizational change to modernize study-team review, patient safety monitoring, clinical signal identification, and real-time decision-making
• Partner with Clinical Science leadership, study teams, Data Management, Biostatistics, Statistical Programming, Digital, Data Science, AI, IT, and Quality
• Serve as Clinical Development business lead for digital, analytics, and AI-enabled capabilities
• Identify and prioritize opportunities involving visual analytics, automation, AI, and digital capabilities
• Lead improvements to clinical data review for usability, consistency, quality, and timeliness
• Implement visual analytics and data-review capabilities for earlier identification of safety signals, efficacy trends, protocol deviations, data-quality issues, and operational risks
• Improve medical monitoring workflows and transition from static reports and manual review to interactive, risk-based approaches
• Partner with Clinical Development Learning on training, communication, change enablement, and adoption
• Represent Clinical Development workflows and scientific requirements in cross-functional technology, digital, and AI initiatives
• Support implementation of new tools and capabilities across Clinical Development
• Develop stakeholder engagement, communication, training, and adoption-tracking plans
• Gather end-user feedback, assess effectiveness, and refine capabilities
• Promote consistent use of approved tools and processes across studies and programs
• Support governance, validation, documentation, and oversight for new capabilities, including AI-enabled solutions
• Monitor external developments in clinical data review, medical monitoring, analytics, and AI
• Establish success measures for adoption, quality, efficiency, and user experience
• Provide strategic direction, line management, coaching, and professional development for direct reports
• Oversee the Innovation Team's project portfolio and align efforts with clinical pipelines and CoE priorities
• Foster scientific curiosity, technical expertise, and collaborative problem-solving

Senior Director, Clinical Data Intelligence, Medical Monitoring Innovation

Director

• Lead the large molecule drug substance portfolio across the global CMO network, primarily supporting commercial technology
• Lead or technically lead process transfer and/or development, scale-up, full-scale production, and commercial lifecycle management
• Manage sourcing, technical transfer, R&D, process improvement and innovation, and troubleshooting projects, with a focus on viral product network transfers
• Conduct spot audits and provide sourcing support
• Lead end-to-end execution after supplier selection, managing internal drug product customers and external suppliers
• Lead Supplier Technical Management for assigned suppliers and selected drug substances
• Lead cross-functional supplier meetings and track changes, deviations, and improvement projects
• Lead process change teams with formulation facilities, regulatory, and quality functions
• Follow up on deviations and ensure timely, appropriate resolution
• Ensure drug substance technology knowledge management
• Develop supplier innovation projects to improve process efficiency and reduce cost of goods
• Guide supplier process development for R&D projects
• Use software systems for supplier communication and change control
• Create project schedules with regulatory, formulation, supply chain, quality, procurement, and R&D input
• Assess manufacturing processes and equipment and mitigate scale-up, transfer, and process-change risks
• Present status updates in governance forums using Microsoft PowerPoint
• Assist supplier troubleshooting communications and conduct facility due diligence visits
• Partner with Network, Global Procurement, Science & Technology, Quality Assurance, and site manufacturing teams

Associate Director – Large Molecule External Manufacturing Technology, Network & Viral Lead

• Support the Outcomes Research Oncology team and the company’s product portfolio, focusing on gastrointestinal malignancies
• Gain experience with real-world data generation, health economic modeling, and reimbursement/health technology assessment requirements
• Contribute to the development and implementation of Outcomes Research and Real-World Evidence programs
• Address value evidence needs of clinicians, key decision makers, and payers
• Write, coordinate, and validate study designs, protocols, data analysis plans, scientific abstracts, and final reports/publications
• Contribute to outcomes research strategies and plans for cross-functional senior management approval

Outcomes Research Intern

Representative

• Work face-to-face with customers in the Springfield, Massachusetts territory
• Understand and identify veterinary clinic, shelter facility, and corporate account customer needs
• Sell the company's Animal Health Companion Animal product portfolio
• Support pull-through activities related to customer strategy
• Position the Animal Health division as a source of value and technical innovation
• Communicate the Animal Health product portfolio in meaningful, customer-relevant ways
• Serve as primary point of contact for assigned customers and meet key personnel and decision-makers
• Understand practice structures, business models, key influencers, customer needs, and business opportunities
• Develop customer strategies for interactions, relationships, solutions, partner involvement, offerings, and sales growth
• Develop territory and account plans for key customers
• Partner with National Account Managers, Corporate Account Team, and Distribution Field Partners on key accounts and corporate-owned clinics
• Collaborate across the organization to increase knowledge of the Animal Health product portfolio
• Share knowledge with regional team members to support team growth and development
• Analyze monthly sales results and manage expenses within budget guidelines
• Identify programs and services to address customer needs and provide education and training opportunities
• Work with leadership and Field Professional Services to develop and deliver relevant customer offerings
• Maintain current knowledge of Animal Health products, industry trends, and competitors
• Communicate relevant customer, industry, product, and market trends throughout the organization
• Develop and meet learning and development objectives agreed with leadership

Companion Animal Territory Representative

Account Specialist

• Serve as a key point of contact for customer accounts in the Pulmonary Arterial Hypertension business
• Generate demand for company products and build relationships with healthcare providers and office staff
• Engage and support account executives who secure formulary access
• Design and execute account strategies addressing local customer needs
• Manage the overall customer experience within target accounts
• Develop account insights, conduct quarterly strategic planning, coordinate account strategy execution, and track progress
• Provide approved disease and product information and resources to patient care teams
• Share target profiles to support identification of appropriate patients
• Educate providers on appropriate product administration and patient support programs
• Coordinate with customer-facing roles to meet care team needs compliantly
• Plan and host medical education events and support company presence at congress and society events
• Build provider-provider connections and partner with headquarters roles on thought-leader events
• Cover the state of Colorado, including Denver, Colorado Springs, Grand Junction, and Fort Collins
• Travel approximately 25% depending on candidate location and business needs

Rare Disease Account Specialist, PAH

Sales

• Engage customers to address identified needs and educate key stakeholders about oncology products
• Communicate with the broader oncology community and achieve or exceed assigned sales goals
• Cover the Cincinnati, Ohio territory, including Dayton, Ohio
• Work with territory team members to attain or exceed assigned geographic sales goals
• Meet key stakeholders to understand practice structure, business models, and influencers while building relationships and trust
• Use approved resources and messaging to communicate patient-centered value of oncology products
• Apply knowledge of multidisciplinary care teams, cancer staging, treatment options, pathways, and guidelines across tumors and diseases
• Analyze trends in complex buying environments, including GPOs, wholesalers, and specialty pharmacies
• Review product purchasing and prescribing patterns across outpatient and inpatient infusion settings, hospitals, and GPO contracts
• Develop and execute short- and long-term plans with the local team and district manager/Oncology Customer Team Leader
• Understand customer priorities and needs through insightful questioning
• Ensure consistent customer experiences across divisions and functions
• Communicate and collaborate with Customer Team Leaders, Key Account Managers, Nurse Educators, Field Reimbursement Associates, Medicare Account Executives, and other customer-team members

Oncology Sales Specialist

Research Scientist

• Provide strategic and scientific biomarker leadership across Neuroscience programs
• Lead the design, execution, analysis, and communication of translational and clinical biomarker strategies
• Develop decision-centric biomarker strategies integrating therapeutic mechanism, disease biology, pharmacodynamics, patient heterogeneity, dose and regimen selection, clinical endpoints, and precision medicine opportunities
• Develop and lead integrated biomarker strategies with cross-functional development teams
• Translate disease biology and therapeutic mechanism into translational hypotheses and fit-for-purpose biomarker approaches
• Define biomarker applications for proof of biology, target engagement, dose and regimen selection, patient stratification, response assessment, and go/no-go decisions
• Serve as biomarker representative on cross-functional program teams
• Partner with Discovery, Clinical Development, Quantitative Sciences, Regulatory, Data Science, Clinical Operations, and other functions
• Lead interpretation of biomarker and clinical datasets and translate findings into actionable recommendations
• Identify disease heterogeneity, therapeutic response, resistance or non-response, and biological drivers of clinical outcomes
• Develop strategies using fluid sampling, imaging, and digital modalities as appropriate
• Evaluate emerging biomarker technologies and analytical approaches
• Communicate strategies, results, risks, and recommendations to cross-functional teams and stakeholders
• Provide scientific guidance and mentorship to biomarker scientists
• Drive publications, scientific presentations, external collaborations, and interactions with external experts

MSD