Serum Life Science Europe GmbH (SLS Europe) is a consulting and service company for the biopharmaceutical industry. We provide tailor-made solutions across the full product development value chain, from bench to market. Our expertise includes regulatory consultancy, translational project management, quality management, and clinical trial oversight. As a subsidiary of the Serum Institute of India Pvt. Ltd., the world’s largest vaccine manufacturer, we are committed to supporting the development and availability of life-saving and affordable medicines globally. To support our team of Project Managers responsible for company and client projects, we are looking for an: Associate Project Manager (m/f/d) Full-time | Office-based in Hannover, Germany | Start: as soon as possible Are you looking for a role where you can apply your scientific background to complex pharmaceutical development projects? Do you enjoy structured thinking, analytical planning, and working across disciplines? SLS Europe offers you the opportunity to take responsibility, contribute to international projects, and grow within an ambitious and experienced team. As Associate Project Manager, you will support the planning, coordination, and follow-up of national and international pharmaceutical development projects. Your tasks will include: Supporting project planning and management activities in areas such as: Manufacture and quality control of medicinal products Non-clinical studies National and international regulatory interactions Clinical trials Supporting project budget, resource, and timeline management Contributing to the planning and facilitation of clinical development activities for innovative medicines from bench to market Reviewing and evaluating project proposals, plans, reports, and project-related documentation Coordinating input from cross-functional teams to help ensure that project milestones are met on time and within budget Supporting national and international collaboration with customers, partners, service providers, and internal stakeholders Contributing to the development and implementation of project management best practices, tools, and templates Completed Master’s degree in life sciences, medicine, pharmacy, or a related field; a doctoral degree or other relevant academic qualification is an advantage Preferably first experience in pharmaceutical research and development, the pharmaceutical/biotech industry, or an equivalent environment Interest in one or more of the following areas: manufacturing, quality control, non-clinical development, clinical trials, or regulatory affairs Excellent self-organization skills and a structured, analytical working style Ability to understand complex scientific and development projects and prioritize required actions Proactive mindset, flexibility, and willingness to take responsibility Enjoyment of interdisciplinary and cross-functional teamwork Strong communication and interpersonal skills when working with stakeholders at different levels Excellent written and spoken English language skills Professional working knowledge of common software packages, especially Microsoft Office; experience with MS Project or other project management tools is an advantage Willingness to travel internationally approximately 4-8 times per year The opportunity to contribute to our mission of making life-saving and affordable medicines available globally Involvement in cutting-edge national and international projects in the pharmaceutical development of vaccines, biologicals, and other medicinal products A diverse, international, experienced, and highly motivated team with a supportive working environment A structured onboarding process, including targeted training and personal mentoring Opportunities for professional development through internal and external training Non-monetary incentives that support sustainability within the company and the environment An office-base...