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Join Minerva Imaging and take ownership of complex projects - driving them from early development through tech transfer to clinical supply as part of our contract development and manufacturing organization (CDMO). Minerva Imaging is looking for a proactive and empathic Project Manager who can lead through influence rather than authority, guiding cross-functional teams in a collaborative and innovative environment. As a Project Manager in our CDMO unit, you will be responsible for leading sponsor-related projects across a multidisciplinary setting, working closely with both internal experts and external partners. Success in this role requires strategic thinking, strong interpersonal skills, and the ability to navigate complexity while keeping people aligned and motivated. You will take ownership of projects spanning early development through technical transfer, ensuring a seamless transition from R&D – whether from sponsors or contract research organizations – into reliable clinical supply. We are looking for someone who can quickly understand new concepts, adapt to changing environments, and confidently navigate complex technical and regulatory landscapes. You may already bring experience from a CRO, CDMO, biotech, or pharmaceutical setting – or you might be an early-career professional with strong curiosity, drive, and the motivation to grow into the role. A solid or developing understanding of CMC and regulatory requirements is expected. If you are eager to join an innovative company that has been recognized with six Gazelle awards for our exceptional growth, we want to hear from you. We welcome both experienced professionals and motivated early-career candidates, and we will align the level and responsibilities of the role based on your experience and potential.
Job Responsibility:
Facilitate efficient transfer of processes and knowledge from sponsors or CROs into the CDMO unit
Lead cross-functional project teams in the development and optimization of radiopharmaceutical products (e.g., radioligand therapies) and manufacturing processes
Drive structured project execution while remaining flexible and responsive to fast change
Ensure alignment on timelines, budgets & quality standards with internal and external partners
Manage CMC-related documentation and support compliance with regulatory guidelines
Interpret and implement relevant regulatory guidelines (FDA, EMA, ICH) into project planning and execution
Contribute to the development of the project management framework, processes and tools within Minerva Imaging
Requirements:
A collaborative team player with the ability to influence, guide, and support others
A master’s degree or PhD degree combined with relevant working experience
Experience in project management or a strong ambition to develop within project management in a CMC/CDMO environment (for junior candidates: demonstrated curiosity, fast learning ability, and motivation to work with complex technical projects is a must)
Understanding (or strong interest in developing understanding) of CMC regulatory requirements and guidelines (e.g., FDA, EMA, ICH) and experience with GMP and CMC-related documentation
Structured and methodical approach to work, with familiarity in project management tools
Strong written and verbal communication skills in English
What we offer:
Flexible working options including the option of working from home