Life Scientist (m/w/d) (Biologe/Biologin)

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...