Eli Lilly

This role is for a Senior/Principal Scientist in Technical Transfer at Eli Lilly, focusing on manufacturing processes for insulin products. The responsibilities include technical support for new product introductions, ensuring accurate documentation and control strategies, and executing validation activities. The role requires a degree in a relevant field, knowledge of GMP and parenteral manufacturing, and strong project management skills.

This role is for an MES System Engineer in the pharmaceutical industry, focusing on designing, developing, implementing, and maintaining Manufacturing Execution Systems (MES) to optimize production processes, ensure data accuracy, and maintain compliance with GMP regulations. The role involves integrating production operations with business systems and collaborating with cross-functional teams.

Senior Scientist role at Eli Lilly in Germany focused on technical leadership and stewardship for aseptic filling processes in a new high-tech production facility. Responsibilities include supporting validation, lifecycle management, process issues, continuous improvement, and ensuring compliance with GMP and regulatory expectations. Requires a degree in a relevant field, professional experience in the industry, and knowledge of GMP operations.

The Sterility Assurance Advisor role at Eli Lilly is responsible for maintaining a safe work environment and understanding the scientific principles required for manufacturing parenteral drug products. This includes using sterility assurance risk management to evaluate manufacturing processes and controls, leading projects associated with sterility assurance programs, and developing/executing process and facility monitoring strategies. The role also involves leading deviations, staying updated on regulatory requirements, influencing corporate guidance, identifying continuous improvements, providing design input for new processes, defending sterility assurance programs during audits, assisting with regulatory submissions, and providing training and technical mentorship.

This role is for a Production Worker in the Parenteral department at Eli Lilly's new high-tech manufacturing facility in Alzey, Germany. The position involves operating machinery, ensuring health and safety compliance, collaborating with team members, following SOPs, troubleshooting issues, and participating in training. The ideal candidate has relevant experience in the pharmaceutical/biotech industry, experience with aseptic filling and/or isolator technology, and knowledge of cGMPs.

This role is for a Senior/Principal Scientist Validation at Eli Lilly's new production facility in Alzey, Germany. The primary focus is on instructing and supporting the validation of production equipment and systems, including sterilization, cleaning, filter, shipping, and process validation. The role involves preparing and reviewing technical documents, participating in process functional teams, and ensuring compliance with GMP and quality objectives. It is an onsite position requiring a degree in engineering or pharmacy with at least 5 years of industry experience and knowledge of GMP operations.

Responsible Scientist role in a Quality Control Microbiology Lab at Eli Lilly, focusing on in-depth problem solving, investigation of aberrant data, technical review, and mentoring lab staff within a GMP manufacturing environment. The role involves ensuring the quality of raw materials, in-process, and finished products.

The role is for a Quality Assurance Technician in a new parenteral manufacturing facility. Responsibilities include on-site quality monitoring during production shifts, material/equipment preparation, formulation and aseptic filling, visual inspection, supporting batch release, GMP documentation, and investigating deviations. The role requires a science/technical background, knowledge of cGMP, and experience in pharmaceutical QA/QC.

This role is for a Packaging Expert - Engineer/Scientist at Eli Lilly in Germany, focusing on device assembly and packaging operations. Responsibilities include technical transfer, process validation, maintaining validated states, establishing metrics, harmonizing control strategies, evaluating process improvements, and providing technical leadership. The role also involves mentoring, floor-level support, risk management, technical documentation, and supporting investigations and audits. Requires a Bachelor's degree in engineering or packaging science with 4+ years of manufacturing experience, preferably in pharmaceutical/medical device packaging.

Senior Manager of Quality Assurance for Parenteral production at a new high-tech pharmaceutical manufacturing site in Alzey, Germany. The role involves leading the operational QA organization, supporting the startup and routine operation of the facility, overseeing quality aspects, and developing a strong quality culture. Responsibilities include managing a team, ensuring compliance with cGMP regulations, and collaborating with cross-functional teams.

This role is for a Sr. Principal Site Molecule Steward at Eli Lilly's new manufacturing site in Alzey, Germany. The position focuses on providing scientific leadership and technical support for drug product manufacturing, acting as a subject matter expert for the site. Responsibilities include ownership of control strategy implementation, technical direction on deviations and change controls, and representing the TS/MS function in regulatory interactions. The role requires a minimum of a bachelor's degree in science or engineering and 5 years of experience supporting parenteral product manufacturing.

Senior Quality Scientist role in pharmaceutical device assembly and packaging, focusing on GMP compliance, quality systems, and regulatory adherence. This role involves overseeing manufacturing processes, investigating non-conformances, managing change controls, and ensuring readiness for inspections. It requires experience in the pharmaceutical industry and a strong understanding of cGMP regulations.

This role is for a Quality Assurance Technician in Device Assembly and Packaging at Eli Lilly's new production facility in Alzey, Germany. The technician will support the startup of the facility, ensure processes and products meet quality standards, monitor production on-site, assist with deviations and investigations, and support batch release. The role requires a technical education or bachelor's degree, knowledge of cGMP practices, and at least 2 years of experience in the pharmaceutical industry with a focus on shopfloor quality assurance.

This role is for a Production Shift Leader in parenteral manufacturing at Eli Lilly's new facility in Alzey, Germany. The position involves leading a team, ensuring safety and quality in sterile filling and inspection processes, and supporting the startup of the facility. It requires experience in sterile filling, production, and leadership, with knowledge of cGMP and FDA guidelines.

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.