Join Minerva Imaging as a Project Manager for our CDMO unit and lead the journey from tech transfer to clinical supply
Minerva Imaging is looking for an experienced Project Manager to join our growing organization and help drive sponsor projects forward in a collaborative and innovative environment.
As a Project Manager for CDMO projects, you will be responsible for leading sponsor projects in our CDMO unit, managing internal and external stakeholders, and cross-functional cooperation. You will lead projects from tech transfer from sponsor or the contract research organization to clinical supply of product. You have a strong background in managing and leading CMC development and manufacturing projects from the CRO/CDMO, biotech or pharma industry. Moreover, you demonstrate a sound regulatory understanding.
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.
About the Role
As a Project Manager for CDMO projects, you will play a crucial role in guiding our projects from the initial tech transfer to the clinical supply of product. You will work closely with both internal and external stakeholders, ensuring seamless cooperation and successful project outcomes.
Furthermore, you demonstrate excellent communication and collaboration skills, which are indispensable in this role. Your ability to effectively set direction, drive progress, and maintain a balance between quality and speed, is highly valued. Respecting and incorporating others' opinions and viewpoints, even when they differ from your own, is crucial.
You will join the Project Management Office and a team of 4 colleagues all dedicated to driving projects forward for the CRO and CDMO units. Moreover, we are continuously optimizing and streamlining the way we work in projects across the organization.
Your key responsibilities will include:
- Facilitate efficient process and knowledge transfer from sponsors or CRO projects to our CDMO unit.
- Lead project teams in the development and optimization of radiopharmaceutical formulations and manufacturing processes.
- Collaborate with partners to meet project timelines, budgets, and quality standards.
- Manage CMC-related documentation and ensure compliance with regulatory guidelines across late-stage development and commercialization activities.
- Interpret and implement relevant regulatory guidelines (FDA, EMA, ICH) into project strategies and execution.
- Contribute to the development of the project management framework, processes and tools within Minerva Imaging.
Qualifications:
- Being a team player who can coach and mentor colleagues, fostering growth both in the individuals and the team
- A master’s degree or PhD degree combined with relevant working experience
- A minimum of 3 years of project management experience driving CMC/CDMO projects.
- Understanding of CMC regulatory requirements and guidelines (e.g., FDA, EMA, ICH) and experience with GMP and CMC-related documentation.
- Broad expertise in utilizing various project tools, coupled with a systematic and methodical approach to work and tasks.
- Strong written and verbal communication skills in English.
Minerva offers:
We believe in creating an agile working environment, so we have flexible working options including the option of working from home. We care about our employees’ well-being and offer health insurance and a quality conscious lunch scheme and monthly social activities.
We are an informal organization with a strong focus on open and honest communication. We value humour and a natural care for one another.
Application:
The application must include a motivated cover letter and a CV addressing the listed qualifications. Applications through LinkedIn are not accepted and will not get a response. Applications will be evaluated continuously. If you have questions regarding the position, please contact Trine Skovlund Neerup at tsn@minervaimaging.com.
Deadline for application: 12-10-2025 via our website: Project Manager for Minerva Imaging CDMO projects I Career Site
About Minerva Imaging:
Minerva Imaging is a scientifically driven and integrated CRO and CDMO specialized in targeted radionuclide therapies. We focus on the use of advanced animal models within oncology, cardiovascular diseases, and in vivo molecular imaging for translational research and drug development. We engage with our sponsors to understand their scientific questions and discuss how our methods and capabilities can provide answers. Our facility located in Ølstykke, Denmark offers best–in–industry fully integrated radiopharmaceutical research, drug development, and manufacturing services.
As part of Minerva Imaging's recruitment policy we expect all candidates to provide their personal criminal record. Minerva Imaging is an equal opportunity employer, and we encourage candidates of all backgrounds and experiences to apply.
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