Eli Lilly

Production operator for packaging area at a pharmaceutical company, responsible for operating and cleaning machinery, following packaging orders, and ensuring quality and safety standards are met.

Senior Advisor, Clinical Research at Eli Lilly, focusing on providing medical expertise for clinical strategic planning and execution in drug development and medical affairs within the Chinese market. Responsibilities include collaborating on clinical trial design and conduct, communicating with health authorities, developing evidence generation plans, supporting brand commercialization, and managing medical meetings and publications.

This role is responsible for building and improving an affiliate risk management environment by leading projects in digital and automation solutions, conducting risk-based monitoring, and driving data intelligence. The position involves cross-functional collaboration to execute risk management strategy and enhance risk detection and prevention capabilities.

This role is for an Engineering Senior Director focused on leading site expansion projects within a pharmaceutical manufacturing environment. It involves project delivery, operational excellence, and effective communication to ensure seamless integration of new facilities into existing operations. The role requires strong engineering and project management experience, particularly in parenteral manufacturing.

This role is in quality assurance within a pharmaceutical company, focusing on the management of lab equipment and systems used for quality control and analytical testing of pharmaceutical products. It involves qualification, maintenance, and retirement of equipment, as well as documentation and process improvement. The role is not directly involved in AI/ML development.

This role is for an Advisor in Technical Services and Manufacturing Science (TSMS) within a pharmaceutical API manufacturing facility. The focus is on laboratory operations, process development, analytical expertise, and ensuring compliance with cGMP regulations. It involves experimental design, data analysis, troubleshooting, and mentoring. The role requires expertise in small molecule and peptide manufacturing, advanced analytical techniques, and regulatory knowledge.

This role focuses on the development and engineering of linker-payload (L-P) chemistry and bioconjugation processes for Antibody-Drug Conjugates (ADCs) and Antibody-Oligonucleotide/siRNA conjugates (AOCs) within a pharmaceutical R&D organization. It involves laboratory experimentation, process design, and collaboration with cross-functional teams to support drug development from early stages through manufacturing.

This role is in Quality Assurance for a pharmaceutical company, focusing on product quality testing, including chemical and microbial analysis, procedure verification, deviation investigation, and change management. It involves collaboration with global teams and potentially team management for higher positions. The role requires experience in QC/analytical testing within the pharmaceutical, medical device, cosmetics, or chemical industries.

This role focuses on the implementation and integration of Manufacturing Execution Systems (MES) and other production IT systems within a pharmaceutical manufacturing environment. The primary responsibilities include bridging business needs with technology, developing and integrating MES components, supporting system startups, ensuring compliance with validation requirements, and evaluating new technologies. The role requires experience with MES platforms and understanding of GMP regulations and Computer System Validation (CSV).

Senior Director for Strategy at Eli Lilly, focusing on external innovation in the China and Asia-Pacific region. The role involves identifying, assessing, and coordinating external search and evaluation efforts for in-licensing opportunities, including agents, technologies, platforms, or targets that align with Lilly's internal R&D pipeline and address unmet patient needs. This includes leading due diligence, partnering with therapeutic area teams, developing relationships within the external pharmaceutical community, and supporting business development initiatives.

Scientist/Sr Scientist role focused on large-scale oligonucleotide synthesis for RNAi-based therapeutic modalities in healthcare. Responsibilities include leading the synthesis scale-up team, developing internal capabilities, collaborating with chemistry teams, and supporting drug candidate discovery. Requires expertise in synthetic organic and nucleic acid chemistry.

This role is for a Technician in Quality Assurance for parenteral manufacturing at a new Eli Lilly production facility in Germany. The primary focus is on ensuring compliance with cGMP standards during the setup and operation of the facility, including material preparation, aseptic filling, and visual inspection. The role involves on-site quality monitoring, deviation management, batch release support, and GMP documentation.

This role focuses on ADME (Absorption, Distribution, Metabolism, and Excretion) and DMPK (Drug Metabolism and Pharmacokinetics) studies for genetic medicines, including siRNAs, ASOs, mRNAs, gene editing, and gene therapy. The scientist will lead studies, interpret data, and collaborate with multidisciplinary teams to support preclinical and clinical development, and prepare regulatory communications. The role requires a PhD and experience in pharmaceutical/biotechnology settings, with knowledge of PK/PD modeling and bioanalytical methods being preferred.

Senior Director role overseeing Operational Controls within the Quality Management System (QMS) for a global healthcare company. Focuses on process excellence, governance, compliance with regulatory standards, and continuous improvement across commercial and clinical supply functions. Requires leadership of Global Process Owners and collaboration with various internal and external stakeholders.

A one-year talent program for junior and senior university students in the pharma sector, focusing on developing future leaders through cross-functional collaboration, project assignments, and training.

Associate Director for Technical Services/Manufacturing Science (TSMS) at a new API manufacturing facility. Responsibilities include managing technical staff, overseeing technical projects, process optimizations, ensuring cGMP compliance, and collaborating cross-functionally. The role involves building the organization and systems for a greenfield startup into GMP operations.

Senior Director role focused on managing and developing strategic alliances with external Contract Development and Manufacturing Organizations (CDMOs) for synthetic molecule design and development (SMDD) in drug substance and drug product. The role involves ensuring capabilities, capacity, and agility in external partnerships to support the development and supply of materials for toxicology and clinical trials, driving novel technologies, operational excellence, and relationship management within a regulated healthcare environment.

Clinical Development Physician role in Neuroscience at Eli Lilly, focusing on leading and supporting clinical development and medical affairs activities for new drugs throughout their lifecycle. Requires a medical license with 5+ years of clinical experience, specialization in neuroscience, and experience in clinical trial support, regulatory submissions, KOL engagement, and scientific data publication. The role involves close collaboration with global teams and supporting post-launch product value enhancement.

This role is for a Sr. Director of Quality Control in API manufacturing at Eli Lilly. It involves strategic leadership for quality control and analytical sciences laboratories, ensuring GMP compliance, and building a high-performing team for a new manufacturing site. The role focuses on operational excellence, regulatory compliance, and personnel development within a healthcare manufacturing context.

Senior Director of Engineering role focused on leading process engineering, automation, and maintenance for a new API manufacturing facility at Eli Lilly. The role involves building the organization, facility, and culture for startup and long-term manufacturing goals, ensuring safety, quality, and operational excellence within a regulated pharmaceutical environment.

Senior Principal Engineer role focused on automation engineering within Biologics manufacturing at Eli Lilly. The role involves providing automation support for operating areas and capital projects, ensuring reliable and compliant control applications and systems. Responsibilities include technical leadership, mentoring, overseeing system integrators, designing and implementing DCS/SCADA software, troubleshooting control loops, supporting electronic systems for data capture, maintaining validated systems, and supporting capital projects. The role requires experience in biopharma engineering, SCADA, DCS, PLC, and MES systems, with a strong emphasis on GMP and computer system validation.

Eli Lilly is seeking an Associate Director for Biotech Operations in Limerick, Ireland, to lead a new, advanced manufacturing facility. This role involves providing technical leadership, managing daily operations, ensuring safety and quality, and building and developing a team. The position requires strong GMP manufacturing experience, leadership skills, and the ability to collaborate with cross-functional teams during the facility's startup phase, focusing on implementing new technologies and processes.

The Senior Director – Quality Control will provide administrative and technical leadership for the Quality Control Labs during the startup, implementation, and operation of a new API manufacturing facility. This role involves managing technical staff, ensuring GMP compliance, overseeing technical projects, and collaborating cross-functionally to meet quality and business objectives in a regulated pharmaceutical manufacturing environment.

Seeking a scientific laboratory leader with a solid background in Neuroscience to join the Psychiatry, Pain and Neuronal Health Team within Neuroscience Discovery Group. The role involves leading a laboratory, developing preclinical in vivo biomarker assays, and contributing to cross-functional teams focused on developing novel medicines for neurological and psychiatric disorders.

Consumer Marketing Manager for Eli Lilly in Czech Republic, Slovakia, and Hungary, responsible for developing and executing marketing strategies to accelerate the reach of medicines, leveraging data analytics, and driving consumer engagement.

This role focuses on ADME (Absorption, Distribution, Metabolism, and Excretion) and DMPK (Drug Metabolism and Pharmacokinetics) studies to support the preclinical and clinical development of genetic medicines at Eli Lilly. The scientist will lead studies, interpret data, collaborate with multidisciplinary teams, and contribute to regulatory communications. The role requires a Ph.D. and experience in ADME or PK/PD within the pharmaceutical/biotechnology industry.

This role is for a Solution Delivery Lead/Manager at Eli Lilly Japan, responsible for leading the execution of IT projects, ensuring alignment between business needs and technical requirements, managing vendors, and overseeing project delivery within budget and on time. The role requires experience in IT project management, system design, development, and implementation, with a strong emphasis on cloud technologies and global communication skills.

This role provides technical leadership and expertise for the manufacturing of peptide Active Pharmaceutical Ingredients (APIs) at contract manufacturers. It involves developing and sustaining process knowledge, ensuring compliance with cGMPs and regulatory expectations, supporting technical transfers, process validation, and process data monitoring. The role also focuses on building relationships, providing process support, leading issue resolution, and driving process optimization and continuous improvement. The ideal candidate will have a strong understanding of manufacturing principles, Lilly systems, and regulatory requirements, with experience in root cause analysis and problem-solving.

This role is for a Supply Chain Planning Associate/Senior Associate at Eli Lilly's Seishin laboratories in Kobe, Japan. The primary responsibilities include planning raw material and intermediate product requirements, purchase timing, and production schedules based on the S&OP process. The role involves ownership as a product leader within the manufacturing division, coordinating with various departments to ensure stable supply of Lilly products. Key tasks include inventory planning, standard production planning, coordinating with international manufacturing sites and global supply chains, risk identification and mitigation, and maintaining/operating production planning systems like SAP and APO. Required experience includes at least 3 years in production planning/execution or procurement/delivery management in a manufacturing company (preferably chemical industry), and strong English and Japanese language skills.

Talent pool for various business areas including Sales, Marketing, Finance, Medical, HR, Regulatory, Legal, Corporate Affairs, Clinical Research, and Quality at Eli Lilly.

This is a reskilling program for individuals with disabilities at Eli Lilly's Kobe office in Japan. The role involves supporting HR recruitment and talent development operations, focusing on general administrative tasks. It requires basic knowledge of HR, administrative skills (Word, Excel), problem-solving, and communication skills. The program is a contract position with a maximum duration of two years.

This is a job posting for back-office positions (HR, IT, Finance, Marketing, etc.) at Eli Lilly in Kobe, Japan, specifically for individuals with disabilities. It requires business-level English and offers various benefits and a standard work environment. The role is not AI-related.