Eli Lilly

Senior Director role in Construction Capital Procurement for Eli Lilly, a global healthcare leader. The role focuses on leading procurement for major capital projects, including engineering, automation, equipment, and construction services, supporting multi-billion dollar expansion plans. Responsibilities include strategic sourcing, project leadership, client engagement, team development, and ensuring compliance within a regulated environment.

Supervisor for Biologics Operations in the Lilly Medicine Foundry, responsible for leading process operators, overseeing safety and quality, ensuring production schedules are met, and managing employee relations in a GMP manufacturing environment. Requires API supervisory experience and experience in biologics/biotechnology processing.

Associate Director of Engineering (Facilities) for a new API manufacturing facility in Houston, TX. This role will lead strategic planning, development, and execution of all facilities management aspects, including maintenance, reliability, and compliance with GMP operations. The position involves supervising engineers, managing external contracts, and ensuring site facilities meet business needs during the startup and operational phases.

Associate role in Parenteral Operations at Eli Lilly, focusing on implementing and monitoring manufacturing projects, driving process improvements, and ensuring a safe work environment. Requires a Bachelor's degree or equivalent experience in Parenteral Operations.

This role is responsible for executing and maintaining global regulatory submissions throughout the product lifecycle, coordinating the creation and legalization of submission documents, and ensuring adherence to regulatory agency electronic common technical document (eCTD) specifications. The role requires technical proficiency in publishing tools like RIM, Adobe Acrobat, Lorenz, and ISIToolbox, and involves collaboration with various internal and external stakeholders to ensure timely and compliant submissions.

This role is for a Pharmaceutical Sales Representative specializing in Gastroenterology. The responsibilities include building customer relationships, conducting technical discussions with healthcare professionals, developing account strategies, and promoting pharmaceutical products. The role requires a background as a certified pharmaceutical representative or a science degree, sales experience, and strong interpersonal skills.

Senior Director role focused on leading embedded systems, manufacturing technologies, automated assembly processes, and global automation/control strategies for drug delivery systems and pharmaceutical devices within a healthcare company. The role involves functional and strategic leadership, defining and governing assembly solutions, and ensuring scalability, compliance, and robustness.

Perform solutions preparations, chemical tests, and analysis of samples in a QC laboratory setting, following analytical methods and SOPs. Requires knowledge of laboratory analysis, methods, practices, and specific chromatography and wet chemistry techniques.

Pharmaceutical Sales- Associate Territory Manager- Cardiometabolic Health role at Eli Lilly. This position involves account-based selling to healthcare providers, promoting priority products, understanding the marketplace, and driving results through Lilly's selling models. The role requires business ownership, strong selling skills, and effective execution to meet sales targets and build customer relationships. It also involves leveraging AI-approved tools and analytical capabilities to streamline customer interactions.

Pharmaceutical Sales Territory Manager for Eli Lilly's Dermatology Specialty division. Responsibilities include account-based selling to healthcare providers, building relationships, understanding the territory and reimbursement landscape, and promoting the product portfolio to achieve sales goals. Requires a Bachelor's degree, valid driver's license, and strong sales and business acumen. Experience in pharmaceutical sales, specialty pharmacy, or selling injectable/infusion molecules is preferred.

The Sr. Director-Medical role at Eli Lilly provides leadership, supervision, coordination, coaching, career development, and performance management for staff within a specified therapeutic or product subgroup of Development. This role involves administrative and technical responsibilities, strategic planning for clinical research and medical support, interaction with external consultants and regulatory agencies, and ensuring compliance with all relevant regulations and company policies. The position plays a significant role in submission, registration, and product launch, and maintains contact with relevant local and global clinical research management, marketing management, and corporate teams. The Sr. Director-Medical also maintains ongoing responsibilities as a Clinical Research Physician.

The Kilo Lab Lead Technician at Eli Lilly supports the startup of a new advanced manufacturing and drug development center (Lilly Medicine Foundry). This role involves bringing manufacturing equipment into service, becoming an expert in assigned areas, and training other technicians. Upon project completion, the technician will provide on-the-floor leadership for API molecule production, ensuring safety and quality. Responsibilities include enforcing compliance, training junior technicians, operating equipment, conducting experiments, dispensing materials, maintaining equipment, leading troubleshooting, and promoting a strong safety culture. The role requires collaboration, creativity, and resilience during the transition from design to operations.

This role focuses on scientific and clinical exchange within the cardiometabolic health therapeutic area, acting as a liaison between Eli Lilly and healthcare professionals (SEs/CEs). The Associate Director will provide in-depth scientific and clinical information, gather insights, and support research and development efforts. The role requires deep content knowledge, continuous learning, and strategic engagement with key opinion leaders.

The Lilly Medicine Foundry Kilo Lab Technician supports the startup and operation of a new advanced manufacturing and drug development center. This role involves transferring chemical processes, operating equipment, conducting experiments, and ensuring compliance with safety and quality standards for clinical supply of various drug modalities. The technician will also support troubleshooting and process improvements.

District Sales Manager for Cardiometabolic Health (Mounjaro) in Hungary, responsible for achieving sales goals, implementing drug strategy, managing a team of medical visitors, and optimizing customer targeting.

Sales Representative role focused on promoting and selling Cardiometabolic health products to healthcare professionals, driving sales growth, and building client relationships. Requires developing sales strategies, identifying business opportunities, and adhering to compliance guidelines.

This is a pharmaceutical sales role focused on promoting Alzheimer's disease treatments within a specific territory. The role involves account management, educating healthcare providers, and driving business results through strategic promotion and understanding of the healthcare ecosystem.

This role is for a Brand Manager in the Cardiometabolic Health division at Eli Lilly, focusing on a flagship Type-2-Diabetes brand in Germany. The position requires full end-to-end responsibility for brand strategy, planning, budget, execution, and performance, involving leadership of cross-functional teams and management of integrated, multichannel campaigns. The role demands strong commercial judgment, deep understanding of the German healthcare environment, and compliance with local regulations.

Logistics Intern at Eli Lilly's Sesto Fiorentino manufacturing site, focusing on raw material management, process optimization, data analysis, and team collaboration within a regulated healthcare environment. Requires a Master's in Management Engineering and strong English skills.

Associate Director of Regulatory Affairs for China at Eli Lilly, focusing on developing and implementing regulatory strategies to accelerate drug submissions, approvals, and launches in the Chinese market. This role involves close collaboration with global and local teams, interaction with regulatory authorities, and ensuring compliance with local laws and Lilly's policies. The position requires expertise in drug development, risk assessment in a regulated environment, and strong communication and negotiation skills in both Chinese and English.

Associate Director, Product Quality & Quality Information (PQQI) at Eli Lilly Japan, responsible for setting strategy and leading teams focused on product quality and quality information management throughout the product lifecycle, ensuring compliance with GQP and Japanese regulatory requirements, driving operational excellence, and supporting product launches.

Senior Application Support Engineer role focused on providing advanced technical support for a suite of products in the healthcare domain. Responsibilities include troubleshooting, diagnosing, and resolving incidents related to application functionality, integrations, performance, and security, acting as an escalation point for L2 support and customer queries. The role involves collaboration with development teams, monitoring application health, maintaining knowledge base articles, supporting deployment activities, and ensuring compliance with regulations like GDPR and HIPAA.

This is a Brand Manager role for a pharmaceutical product (Kisunla) in the Neuroscience division, focusing on strategic brand planning, launch preparedness, and lifecycle management for Alzheimer's disease treatments. The role involves managing the brand P&L, stakeholder relationships, and ensuring compliance with regulatory requirements.

Apprenticeship role focused on electrical instrumentation maintenance within a regulated GMP environment at a pharmaceutical manufacturing site. Responsibilities include supporting repair, replacement, installation, and maintenance of equipment, working with industrial control systems, interpreting schematics, and analyzing system faults.

Apprenticeship role focused on mechanical automation and maintenance fitting within a regulated GMP environment to support production activities. Responsibilities include installation, repair, and maintenance of plant and machinery, working with various machine tools, and understanding technical drawings.

This role is for a Chemist Laboratory position at Eli Lilly in Puerto Rico. The primary responsibilities include ensuring laboratory compliance with regulations, reviewing analytical results, generating and reviewing laboratory documents, and providing analytical and technical support. Requirements include a Bachelor's or Master's degree in Chemistry, a chemist license, and at least three years of experience in a manufacturing environment. The role emphasizes leadership, customer focus, continuous improvement, computer literacy, teamwork, and strong communication skills. Bilingualism is also required.

This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health division. Responsibilities include achieving sales targets, building and maintaining customer relationships, providing product information, and gathering market intelligence. A bachelor's degree in a pharmaceutical-related field and prior sales experience are preferred.

This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health division. Responsibilities include achieving sales targets, building and maintaining customer relationships, providing product information, gathering market intelligence, and collaborating with internal teams.

Lead Analyst for Cyber Threat Intelligence (CTI) at Eli Lilly, focusing on strategy, operations, and team development. This player/coach role involves hands-on technical leadership in threat analysis and attribution, while also shaping the function's strategy, developing analysts, and representing the team in various forums. Responsibilities include threat actor tracking, brand and executive protection, partner collaboration, intelligence sharing, team leadership, and enhancing tooling for automated enrichment and response workflows.

Supervisor providing leadership and direct management to process operators in the Medicine Foundry operations group, overseeing the production of API molecules with a safety-first, quality-always approach. Responsibilities include enforcing compliance, overseeing operations, leading safety culture, troubleshooting process upsets, reporting safety and quality events, managing shift communications, and ensuring personnel follow cGMP practices.

This role provides support in the implementation of research studies in Mexico, focusing on administrative and regulatory activities. The intern will gain knowledge of the regulatory, logistical, and administrative processes involved in research protocol development and implementation, ensuring compliance with national and international regulations.

This role is a senior operational and strategic leader accountable for the end-to-end process and systems architecture applied by Exploratory Medicine and Pharmacology (EMP). It ensures EMP can deliver its clinical portfolio compliantly and efficiently through external vendors and CRO partners, while remaining aligned to Lilly's internal quality and regulatory frameworks. The role involves process and systems integration, compliant outsourcing process design, and acquisition/program integration.

This role owns and leads the entire digital strategy for healthcare professionals (HCPs) not visited by sales reps, focusing on measurable prescription impact through digital channels. It involves designing and implementing digital engagement models, tracking performance outcomes, leading agencies, developing data analysis frameworks, optimizing expenses, and acting as the digital business owner to influence omnichannel strategy and future planning.

Associate Director, Clinical Development Trial Lead (CDTL) at Eli Lilly, responsible for leading cross-functional teams in the development and execution of complex clinical trials. This role involves project management, risk assessment, budget management, and ensuring trial quality, timeliness, and adherence to scope and budget. The position requires deep understanding of clinical drug development processes and regulatory requirements to ensure inspection readiness and drive continuous improvement.

This is an accounting intern position at Eli Lilly, a global healthcare company. The role involves controlling and accounting for expense reclassification requests, bank account reconciliation, import control, freight and storage reconciliation, monthly industrial research data, purchase order control for the accounting department, and supporting internal and external audits. Requires a degree in Accounting with a completion forecast from December 2027, intermediate English, and desirable Excel skills.

Operator role in biotechnology manufacturing, responsible for performing production tasks, following GMP, and ensuring safety and quality. Requires an Associate's degree and experience in fermentation or isolation.

Student internship role focused on digital marketing, omnichannel strategy, and AI within the Specialty Business Unit (Oncology, Immunology, Neuroscience) at Eli Lilly. The role involves supporting digital engagement, campaign execution, expanding reach, contributing to omnichannel strategy, and collaborating cross-functionally. Familiarity with AI and digital tools is a plus.

This role is for a Medical Science Liaison (MSL) in Sweden, focusing on incretins. The MSL will be a field-based scientific expert, facilitating communication between Lilly and healthcare professionals, providing in-depth scientific information, and gathering insights. Responsibilities include maintaining deep scientific knowledge, engaging with experts, supporting research studies, and managing a territory strategically. Requires an advanced degree in Health Sciences with relevant experience, strong communication and interpersonal skills, and adherence to ethical and regulatory standards.

Executive Medical Director role in Early Clinical Development for the Immunology team at Eli Lilly, focusing on developing transformational medicines for autoimmune and inflammatory diseases. The role involves strategic leadership, designing and executing early clinical studies, integrating translational endpoints, and collaborating with cross-functional teams, regulatory affairs, and external experts. Requires a physician scientist with strong clinical translational experience and leadership skills.

This role is for a Visual Inspection Operator in a pharmaceutical manufacturing site. The primary responsibilities include safely inspecting high-quality pharmaceutical products using Lilly standards, operating automated and semi-automated equipment, and adhering to Good Manufacturing Practices (GMPs). The role requires strong attention to detail, basic math and computer skills, and the ability to work in a manufacturing environment. Experience with GMPs and pharmaceutical manufacturing is preferred.

Associate Director for Biotech Operations at Eli Lilly, leading manufacturing operations and cross-functional process teams in a new, advanced biotech facility. Focuses on daily operations, people management, site leadership, and startup priorities, ensuring safety, quality, and productivity.

Associate Vice President for Health Economics and Outcomes Research (HEOR) in the Oncology Business Unit, responsible for global HEOR strategy and execution. This leadership role involves partnering with cross-functional teams to build a strong evidence base supporting the clinical and economic value of oncology medicines, managing the HEOR program end-to-end, and ensuring alignment with asset milestones and payer access needs.

Senior/Principal Process Engineer at Eli Lilly focused on API External Manufacturing for Peptides. The role involves providing technical leadership and expertise to contract manufacturers, ensuring reliable supply and commercialization of medicines. Key responsibilities include developing and sustaining process knowledge, coaching team members, leading tech transfers and scale-up, supporting process optimization, ensuring equipment capability, and overseeing health, safety, and environmental (HSE) and process safety management (PSM) elements at contract manufacturing sites. The role requires a strong understanding of chemical engineering principles and experience in a regulated manufacturing environment.

Internship role supporting the Human Resources team at Eli Lilly, focusing on core HR operations, employee lifecycle processes, recruitment support, HR metrics tracking, and contributing to HR process improvement, AI, and automation projects.

Associate Director - Digital & Data Lead at Eli Lilly, responsible for overseeing and aligning digital programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. The role involves championing digital plant strategy, influencing senior leadership on technology direction, providing input to business and strategic financial plans, and ensuring GxP compliance for all digital solutions. This position requires a deep understanding of manufacturing, lab, and quality processes, and the ability to translate business needs into actionable digital strategies.

Territory Manager role focused on enhancing customer experience by identifying needs and delivering pharmaceutical healthcare solutions to achieve business objectives. Responsibilities include analyzing market trends, developing sales plans, engaging with doctors and other stakeholders to promote company products, and achieving sales targets within the assigned territory in India.

This entry-level role supports the development, configuration, and localization of global manufacturing applications on the Tulip platform, aiming to eliminate paper-based processes. The associate will contribute across the full delivery lifecycle, including requirements, configuration, validation, deployment, and support, while adhering to GxP and data integrity principles. The role also involves exploring AI-assisted development and AI/automation use cases to advance paperless manufacturing goals.

The Sr. Principal Scientist, Advisor role in Global Regulatory Affairs (GRA) at Eli Lilly focuses on providing strategic and operational direction for Chemistry, Manufacturing, and Controls (CMC) development and regulatory strategies for market registrations and lifecycle maintenance in the EMEA region. This involves deep knowledge of global and regional regulations, manufacturing processes, and collaboration with various internal and external stakeholders to ensure timely and successful product registrations.