Eli Lilly

Senior Director of Health, Safety & Environmental (HSE) for a new state-of-the-art oral solid dosage manufacturing facility in Katwijk, Netherlands. This role leads the EHS function, ensuring compliance with Dutch and EU regulations, developing safety strategies, and integrating EHS into all aspects of the site's operations, from design to start-up and ongoing manufacturing. The position requires strong leadership, strategic planning, and experience in pharmaceutical manufacturing environments.

Associate Director - IT Systems Delivery Lead for a global healthcare leader in the pharmaceutical industry. This role will oversee and align multiple programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. Responsibilities include program management, release train engineering, GxP compliance, stakeholder management, risk management, resource allocation, and reporting. Requires a strong business understanding, analytical skills, and the ability to manage large-scale, cross-functional projects. Experience in Pharma and GMP Manufacturing is required.

This role is for a (Senior) Advisor-Medical Affairs CMH in Primary Care at Eli Lilly, focusing on the CardioMetabolic Health portfolio. The individual will act as a medical expert, translate clinical insights into strategies, manage relationships with healthcare professionals, and contribute to medical strategy development and execution within the primary care setting. The role requires a medical degree (BIG registration) and experience in CMH-related care, preferably in primary care or the pharmaceutical industry.

Senior Director role responsible for the technical strategy and process excellence of drug product manufacturing at an Oral Solid Dosage manufacturing site. This includes technical oversight for drug product intermediates control strategy from spray dried dispersion through tablet and capsule manufacturing. Serves as the site’s authority on technology transfer, scale-up, and manufacturing science for oral solid dose forms (tablets, capsules).

Senior Director of Quality Assurance for a new pharmaceutical manufacturing facility in Katwijk, Netherlands. Accountable for setting and executing the site's QA strategy, ensuring cGMP compliance, regulatory readiness, and fostering a strong quality culture. This role involves executive quality leadership, governance, compliance, operational oversight, talent development, strategic planning, and EHS accountability within a highly regulated pharmaceutical manufacturing environment.

This role is for a Sr. Director of Project Management within Global Facilities Delivery at Eli Lilly, focusing on delivering large capital assets for medical innovation and medicine supply chains. The position requires leading cross-functional teams to manage projects from conceptual design through operational qualification, ensuring safety, cost, schedule, and quality. Key responsibilities include stakeholder communication, compliance with company policies, and developing safety/environmental execution plans. The role is based in various locations including the Netherlands and US, with travel flexibility required.