Minerva Imaging’s vision is to become the leading contract research and contract development organization for targeted radionuclide therapy and imaging, enabling improved treatment regimens for cancer patients.
We aim to excel in delivering customized cancer radiopharmaceutical research and serve as an extended research team to our collaborators. We have built a global leading R&D platform for targeted radionuclide therapy and Contract Development and Manufacturing (CDMO) to enable integrated planning and faster execution of promising new radionuclide theragnostic projects in close collaboration with leading researchers, biotech, and pharmaceutical companies.
We are in a fast-paced environment, where our scientists and technicians directly impact the advancement of new improved and lifesaving drugs for cancer patients. We have the ambition to make a difference for our clients, collaborating on advancing new treatment modalities for patients.
As Head of Production, you will oversee the daily operations of our GMP manufacturing processes for radiotherapeutic compounds. You will lead a dedicated team of technicians and scientists, ensuring consistent quality, on-time delivery, and continuous process improvements. In this role, you will also serve as a primary point of contact for our clients, providing clear, professional communication regarding project status, timelines, technical requirements, and any deviations. You will collaborate closely with client representatives during technology transfers, scale-up activities, and routine production to ensure their expectations are fully aligned with our operational capabilities.
The ideal candidate is a strong team player with excellent communication skills, a keen eye for detail, and a commitment to efficiency, upholding the high standards of quality and data integrity for which we are known. You will be leading an experienced team, and your role will, among other things, include:
- Lead and oversee GMP manufacturing operations, including planning, coordination, and resource allocation.
- Ensure compliance with GMP regulations, regulatory requirements, and internal SOPs.
- Manage, develop, and motivate the production team.
- Contribute to project management for technology transfers, process scale-up, and new production lines.
- Collaborate with QA, QC and CMC to ensure smooth operations.
- Identify and implement process improvements with a focus on quality, efficiency, and safety.
Qualifications:
- Degree in pharmacy, chemistry, biotechnology, or related technical/scientific discipline.
- Minimum 5 years experience in GMP manufacturing within the pharmaceutical industry, ideally with radiopharmaceuticals or sterile products.
- Proven leadership experience with direct staff management.
- Strong project management skills and experience with technology transfer.
- Solid understanding of regulatory requirements and inspection processes.
- Fluency in English (written and spoken)
As a person, you:
- Structured and decisive, with an eye for both detail and the bigger picture.
- Ability to create a positive and results-driven work environment.
- High level of responsibility and integrity.
- Proactive and solution-oriented, with a focus on continuous improvement.
- Flexible and adaptable and able to quickly adjust to changing tasks, processes, or priorities.
Minerva offers:
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:
Please submit your application to us no later than 15th of September. The application must include a motivated cover letter and a CV addressing the listed qualifications. Applications will be evaluated continuously.
If you have questions regarding the position, please contact Camilla Christensen, Head of CDMO at cch@minervaimaging.com
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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