Eli Lilly and Company

General Counsel

• Develop strategy for, manage, and advise senior leadership and the business on litigation, investigations, pre-litigation disputes, and other high-risk matters in the United States and elsewhere
• Collaborate with cross-functional colleagues to provide practical and thoughtful legal counseling on a variety of business initiatives, emerging risk issues, and risk assessments
• Actively engage with and manage outside counsel, including by assembling virtual law firms, developing and managing to reasonable budgets, and aligning litigation strategies with business priorities
• Build and maintain relationships with key internal stakeholders
• Engage with key external parties and entities, including government agencies, industry groups, and outside counsel networks
• Review, analyze and keep current on litigation developments affecting the pharmaceutical industry

Senior Director – Counsel – Litigation & Investigations

Operations

• The Supervisor provides leadership and direct management to the process operators in the Medicine Foundry operations group.
• The Manufacturing Supervisor actively supports and oversees start-up activities to bring manufacturing equipment into service.
• The Supervisor leverages knowledge on their team and educates the team on the proper operation of the facility.
• This role requires domestic and international travel to collaborate, train, and learn from sites that currently produce APIs.
• Upon completion of the project phase, the Supervisor oversees the production of API molecules.
• The Supervisor ensures the team consistently employs a safety-first, quality-always approach while managing a production process that encompasses diverse unit operations and manufacturing skills.
• Responsible to enforce adherence to compliance requirements (safety, quality, and environmental) and appropriately escalating any adverse events.
• Overseeing operation of processes and equipment according to batch records, user manuals, design parameters, standard operating procedures, and work instructions to meet production schedule.
• Oversee monitoring, testing, cleaning, and operation of area equipment and systems.
• Ensure all systems are in good operating condition and maintained per applicable requirements.
• Serve as a key leader for site safety culture, promoting compliant operations and positive safety behaviors.
• Lead by example and promote accountability at all levels.
• Provide technical leadership for troubleshooting and reaction to process upsets, integrating operator input and escalating as appropriate.
• Follow all applicable procedures for safety event reporting and documentation.
• Follow all applicable procedures for quality event reporting and documentation.
• Oversee communication between shifts regarding the status of area operations and addressing any issues/problems that have occurred at shift passover.
• Participating in daily shift huddles/meetings to understand and set expectations for daily operational goals.
• Lead and make assignments for building and area operations such as safety audits, procedure coordination, housekeeping, and continuous improvement projects.
• Ensure all area personnel follow cGMP practices, safe work habits, plant dress code, hygiene standards, and housekeeping requirements unique to the work area and job classification.
• Enforce use of specified company-supplied personal protective equipment (PPE) as required.
• Responsible for the effective deployment of operators to meet production schedules, maintaining adequate cover for Emergency Response Teams, managing holiday and overtime levels across process and production operators, timecard and coding for process operators.
• Responsible for individuals’ performance on shift, managing employee relations and completing annual performance management processes.
• Ensure that all shift members are appropriately trained, and that operating procedures and training material are available and current.
• Partner with area Associate Director to understand Foundry strategy and future production needs.
• Represent and support this strategy in conversations with shift members.
• Manage collaborations between the shift and functional support groups such as maintenance, engineering, analytical laboratory, and Technical Support.

Supervisor, Hybrid Operations

Compliance

• Lead the digital transformation and automation agenda across Global Regulatory Affairs
• Drive implementation of AI/ML applications, advanced analytics and digital capabilities that accelerate regulatory delivery
• Establish performance metrics and real-time dashboards that track organizational effectiveness and demonstrate business impact
• Translate strategic digital and operational visions into tactical execution plans
• Drive end-to-end implementation of approved digital and operational initiatives across GRA
• Develop and implement comprehensive change-management plans including communication strategies and training programs
• Monitor external environment for novel digital trends, tools, and methods

Associate Vice President – Head of Digital Strategy and Innovation

Engineer

• Be the SME with a deep technical expertise in all systems under his/her responsibility
• understanding their applications in pharmaceutical manufacturing, understanding flow charts and process parameters, and awareness of industry trends
• Monitor all systems associated with the HYB and maintain KPI’s to assure that they are operating properly and in compliance with internal and external requirements.
• Act as the single point of contact for the HYB in order to ensure compliance related activities such as deviations, change controls and CAPA’s are resolved and implemented in conjunction with Operations, Process Engineering, Supply Chain, HSE and Quality Assurance.
• Apply “hands-on” problem solving skills in quickly and efficiently resolving equipment failures, troubleshooting.
• Provide internal customer consultation and notifications on issues that involve critical utilities and equipment associated with the HYB.
• Assure that all necessary corrective / preventive maintenance items are identified on the proper tracking systems, and ensure activities are completed by the required dates.
• Lead or participate in capital projects / changes for all systems under his/her responsibility in the HYB including project management, design, resource planning, budget adherence and Qualification/Verification activities (IQ/OQ/PQ).

Area Engineer – Hybrids Building

Manager

• Leads the cross-functional study team in clinical trials development and execution
• Accountable for delivering trials with quality, on time, and within scope and budget
• Coordinates efforts to achieve or exceed trial deliverables
• Manages budget components and monitors trial-level risks
• Acts as a single point of contact for trial communication and relationships

Associate/Senior Associate, Manager – Clinical Development Trial Lead

Account Executive

• Know and stay up to date on the products being promoted, and on diseases and treatments related to diabetes and obesity
• Stay informed about the pharmaceutical market and competitors
• Conduct territorial analysis using reports provided by the company
• Manage physician records based on territorial analyses and field knowledge
• Visit physicians to promote the product line, provide relevant technical information, and build relationships
• Implement events: contact speakers, schedule venue and date, invite physicians, and execute events locally in-person or virtually
• Prepare reports of visits, sales, and expenses for management control

Mid-level Sales Representative – Cardiometabolic

QA Engineer

• This position is responsible for developing and carrying out the control strategy, routine quality oversight, risk management, and continuous improvement of a globally based large network of Radiopharmaceutical contract manufacturers for the reliable supply of investigational and commercially approved Lilly compounds, out licensed and externally purchased products.
• This role ensures phase appropriate CDMO qualification and third-party quality oversight is established and remains successful.
• This position defines goals in support of company objectives and collaborates with Global Quality Systems for developing or effectively integrating the unique challenges with radiopharmaceuticals with company standards.
• The individual works closely with R&D, CMC, Global External Manufacturing, Lilly Affiliates, leadership, and project teams to plan for and execute these responsibilities.
• This role interfaces with external trade and pharmaceutical associations to support the evolving Radiopharmaceutical regulatory landscape, new product innovation, articulating unique guidelines for the manufacture of radiopharmaceuticals, and the global delivery of products.
• As lead of global contracted radiopharmaceutical manufacturing, this role is responsible for organizational and resource management, staff development, and career planning.
• The individual manages a functional team of professional staff responsible for establishing the quality oversight strategy and maintaining drug product CDMOs manufacturing at various stages of development from Phase 1-3 and commercially marketed products.
• This position works with business and compliance team members to identify solutions including automated and AI opportunities to drive efficiencies in work effort, time, right first time, and an increase in productivity.

Senior Director – Quality Assurance, Radiopharmaceutical External Manufacturing

QA Automation Engineer

• Mentor process control team, including design, controls philosophy, implementation and commissioning
• Process control work implementation and coordination
• Review and monitor financial performance; commit to meeting targets
• Develop and implement the Automation Engineering Project Plan.
• Technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications.
• Lead/Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs
• Lead a team of automation engineers supporting commissioning
• Provide periodic status updates to Project Management
• Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering
• DCS and SCADA software design, coding/configuration and testing (sequence logic, graphics, batch software etc.)
• Perform automation engineering activities including design, tuning and troubleshooting of control loops
• Implement and support electronic systems (such as plant historians, applications and software integration) used to capture process automation related production data
• Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation
• Automation support for capital projects including new product introductions
• Promoting the use of automation to improve productivity, operational efficiency and compliance
• Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed
• In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.
• Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines.
• Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement
• Demonstrated ability to influence peers and business partners
• Good written and verbal communication skills for both technical and non-technical audiences

Advisor Engineer – Automation Engineering

Project Manager

• Lead study teams in the planning and execution of Phase 1 clinical studies
• Manage study timelines, risk, and budget
• Serve as the trial level owner of communication across functional personnel
• Proactively identify and communicate project status, issues, and risks
• Provide oversight and approval of cross-functional vendor results
• Work with exploratory and bio-pharmaceutics clinical development colleagues to acquire study cost estimates
• Track study-level spending and change needs
• Initiate contracts with investigators and external entities
• Ensure site initiation, monitoring and closeout visits are performed
• Provide scientific consultation for clinical and regulatory documents

Clinical Trial Project Manager, Clinical Delivery

Director

• MSLs will be required to engage in continuous learning to maintain the highest level of technical expertise within the therapeutic area they represent.
• MSLs will spend the majority of their time on customer facing activities.
• MSLs will be expected to demonstrate strategic analysis, planning, and prioritization to maximize efficiency.
• MSLs effectively synthesize and communicate actionable customer/clinical insights to internal Lilly medical and cross functional teams.
• MSL will execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws.

Associate Director – Medical Science Liaison, Rheumatology

• Work with a team of experienced professionals to help clients optimize information governance/records and information management practices
• Contribute directly to delivering first class services to our clients
• Lead delivery of multiple simultaneous large enterprise-wide projects
• Provide Technical SME support and consultation across Records Management domains
• Lead engagement planning, budgeting, and economics
• Develop and lead strategic solutioning across RIM initiatives
• Be responsible for day-to-day interactions with internal clients and Lilly teams
• Facilitate consensus of proposed solutions from senior client collaborators
• Perform Corporate RIM Due Diligence on potential acquisitions

Associate Director – Global Records Information Management

Account Manager

• The Key Account Manager will be responsible for managing, developing, and growing strategic accounts within pharmacy chains/distributors and emerging channels.
• Develop and execute Joint Business Plans (JBPs) with assigned pharmacy chain accounts.
• Build and maintain strong, long-term relationships with key decision-makers and stakeholders within pharmacy chains.
• Lead commercial negotiations, ensuring win-win outcomes aligned with Lilly’s business objectives.
• Analyze market trends, sales data, and account performance to identify growth opportunities.
• Coordinate cross-functional collaboration with Sales, Marketing, Finance, Supply Chain, Market Access, and Medical teams.
• Ensure excellence in execution of commercial strategies at account level.
• Monitor KPIs, forecast sales, and manage budgets for assigned accounts.
• Act as the main point of contact between Lilly and assigned key accounts.

Key Account Manager

• Establish and sustain strong, trusted relationships with haematologists, clinical nurse consultants, pharmacists, and multidisciplinary teams across hospital and specialist settings
• Navigate complex pathways within accounts, identifying opportunities to enhance the patient experience and drive positive outcomes in readiness for an upcoming launch
• Serve as a strategic partner to clinicians and accounts, aligning our commercial approach to support both patient and business objectives
• Demonstrate a deep understanding of Haematological malignancies and benign Haematology disease areas relevant to the portfolio
• Confidently and compliantly communicate clinical evidence tailored to customer needs
• Develop and execute a robust territory business plans aligned to national brand strategy and local insights
• Collaborate closely with internal colleagues to ensure the seamless execution of initiatives and deliver outstanding customer satisfaction

Haematology Business Manager

• The Clinical Research Scientist applies scientific and clinical expertise as a key member of the Medical Affairs team, supporting healthcare readiness, product launch, commercialization, and development activities.
• The CRS serves as a strategic partner to brand teams, development groups, and regulatory functions while ensuring all activities comply with regulations, Good Clinical Practices (GCPs), and company policies.
• Address scientific and clinical information needs of patients, healthcare providers, and payers related to disease states and specific molecules.
• Contribute medical expertise to brand commercialization strategies and business planning.
• Support pricing, reimbursement, and access (PRA) initiatives with clinical insights.
• Partner with corporate affairs regarding advocacy, communication, and environment shaping.
• Engage with healthcare professionals to gain insights into key medical questions.
• Review and approve promotional materials.
• Train sales representatives and medical staff.
• Participate in trade associations as appropriate.
• Respond to unsolicited scientific inquiries from healthcare professionals per compliance guidelines.
• Plan and support symposia, advisory boards, and professional meetings.
• Present data at congresses and conferences.
• Generate scientific disclosures that address key therapeutic area needs.
• Develop relationships with key opinion leaders and scientific experts.
• Prepare publications, abstracts, and scientific presentations.
• Collaborate with global teams on late-phase clinical trials.
• Support preparation and review of local product labeling.
• Maintain deep knowledge of local labels and competitive landscape.
• Generate and share relevant medical information emanating from clinical trials.
• Partner with Real World Evidence teams for data addressing key disease state or asset evidence needs.
• Stay current with medical literature and therapeutic area developments.
• Monitor competitive products and emerging trends (1–5-year outlook).
• Attend scientific congresses and pursue external learning opportunities.
• Serve as scientific consultant to study teams.
• Support medical budget preparation and administration.
• Coach and provide feedback to colleagues and direct reports (if applicable).

Director – CRS-US & Global Med Affairs, NBU, Psych & Substance Use Disorders

Content Marketing Manager

• Serve as enterprise system owner for the AI-powered learning platform (i.e. Sana, Docebo, Absorb), handling performance, upgrades, vendor coordination, and system usage education
• Lead the strategy for functional system settings, integrations and workflows to support evolving L&D strategies and compliance requirements
• Serve as the global lead for resolving platform issues, ensuring learner impact is minimized through effective coordination with support teams
• Establish systems and tools to supervise platform usage data and recommend enhancements through organizational change processes
• Develop and implement the hosting and eLearning technical standards portion of the content management strategy for global and business learning content
• Partner with IT, GLCS and Business L&D to guide decisions and establish requirements for content hosting, system and partner integrations and troubleshooting
• Define learning platform standards for content formats (e.g., SCORM, xAPI), accessibility, and hosting
• Ensure content is organized on servers, aligned with technical standards, and optimized for global use based on storage and access, as well as handled according to global records retention requirements
• Guide L&D teams on eLearning technical standards and platform capabilities
• Author and maintain guidelines and job aids for hosting and eLearning standards supporting content development and deployment
• Collaborate with IT, HR, vendors, and L&D teams to align platform initiatives with business needs
• Coordinate collaborator input for system enhancements and process improvements, including the SuccessFactors LMS and the Global Learning Content Services team
• Ensure seamless integration with enterprise systems and data flows
• Represent global business needs in platform decisions and strategy
• Drive continuous improvement initiatives to enhance learner experience and platform effectiveness
• Ensure consistent standards and scalable solutions across regions
• Conduct ongoing external benchmarking and market scanning to stay apprised of emerging learning technologies, AI capabilities, and industry protocols, ensuring Lilly’s learning ecosystem remains innovative, driven, and future-ready