About us

Minerva Imaging’s vision is to become the leading contract research and contract development organization for targeted radionuclide therapy, enabling improved treatment regimens for cancer patients with a focus on the use of advanced animal models within oncology and cardiovascular diseases and in vivo molecular imaging for translational research and drug development.

Click here to apply.

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 now add 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.

Minerva is at the forefront of R&D in the theragnostic area. We are in a very fast-paced environment, where our researchers directly impact the advancement of new improved, and lifesaving drugs for seriously ill cancer patients. We have the ambition to make a difference for our clients, collaborating on advancing new treatment modalities for patients.

Our plans for the new Production/QC Scientist CDMO

The role will support Minerva Imagining for the establishment of its new expanded cGMP radiotracer production. The job will involve working with radiation with all appropriate health and safety measures in place.

As a Production/QC Scientist CDMO, you will be a key team player in the development of the GMP supporting structure needed to ensure high-quality and efficient outcomes. You will take responsibility for the daily operations at our manufacturing site and collaborate with technology transfers. As a key scientist in manufacturing and QC you will drive some of the processes related to products to be onboarded at our state-of-the-art facilities/equipment.

The ideal candidate has a strong scientific understanding of GMP processes and, preferably, some experience related to production processes involving radio metals. A high level of GMP writing skills is also expected. Your interest in quality assurance and your dedication to delivering high-quality work is more important than many years of industry experience.
As an individual, you are detail-oriented, thorough, reflected, and work structured with a persistent attitude and a critical thinking mindset to deliver high-quality work. You are a relaxed, kind, and a great team player.

You will be joining a team that is composed of 4 highly skilled and committed professionals that integrate key competencies required to be a best-in-class radiopharmaceutical CDMO.

Tasks:

• Drive the scientific tracer development Support initial production batches for validation for Minerva Imaging regulatory approvals.
• Support chemistry development work for new metal-based tracers as per the Minerva Imaging project pipeline
• Lead technical feasibility and optimization of radionuclide production.
• Support GMP compliance programs both for manufacturing and QC.

Experience

• GMP radiopharmaceutical production
• Radiometals, including nuclide production/purification and tracer labeling.
• GMP experience or other significant GMP insight
• Analytical chemistry or isotope production and characterization
• Writing GMP documents.

Qualifications:

• Chemist/Physicist (min. MSc)
• Problem-solving and make-it-work attitude.
• Good team player and eager to learn
• Strong analytical skills and attention to detail
• Thrive in a fast-paced and service-oriented organization.
• English is required, and Danish is an advantage.

Please submit your application no later than February 21st, 2023, by applying the link. The application must include a motivated cover letter and a CV addressing the listed qualifications. Applications will be evaluated continuously, and potential candidates will be invited for job interviews in week 8 and 9.

About Minerva Imaging
Minerva Imaging is a scientifically-driven CRO founded in 2011 counting 130 employees. Our focus is on the use of advanced animal models within oncology and cardiovascular diseases and in vivo molecular imaging for translational research and drug development.

We engage with our collaborators to understand their scientific questions and discuss how our methods and capabilities can provide answers. We are rapidly growing, and the right candidate will be a key contributor to maintaining the scientific foundation and our approach to research while expanding our business. You will join a highly specialized CRO/CDMO, with ambitions of taking disease treatment to the next generation of personalized medicines.

We are an informal organization with a strong focus on open and honest communication. We value humor and natural care for one another, meaning stepping up and lending a helping hand to a colleague when needed.

Follow Minerva Imaging on LinkedIn for the latest news.

Click here to apply.

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 focus on using advanced animal models within oncology and cardiovascular diseases and in vivo molecular imaging for translational research and drug development.

Click here to apply.

We aim to excel in delivering customized cancer radiopharmaceutical research and serve as an extended research team to our collaborators. We have built a leading global 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.

Minerva is at the forefront of R&D in the theragnostic area. We are in a very fast-paced environment where our scientists directly impact the advancement of new, improved, and lifesaving drugs for seriously ill cancer patients. We have the ambition to make a difference for our clients, collaborating on advancing new treatment modalities for patients.

Our plans for the new Production QC technician for CDMO

The role will support Minerva Imagining for the establishment of its new expanded cGMP radiotracer production. The job will involve working with radiation with all appropriate health and safety measures in place.

As a Production/QC technician for CDMO, initially -till we will achieve the milestone of having GMP accreditation-, you will be a key team player in the development of the GMP supporting structure needed to ensure high-quality and efficient outcomes. Once GMP-operation starts, you will take part in the daily manufacturing and QC tasks at our new site. You will also be involved and collaborate with developments within technology transfer tasks needed for processes to become established within GMP standards.

The ideal candidate has a strong background as a technician in the production of radiopharmaceutical products, preferably with a good understanding of GMP-processes. Experience related to processes involving radio-metals is an advantage for this role.

As an individual, you are detail-oriented, thorough, reflected, work structured with a persistent attitude and a critical thinking mindset to deliver high-quality work. You are a relaxed, kind, and great team player.

Your interest in quality assurance and dedication to delivering GMP high-quality work is more important than many years of industry experience.

You will be joining a team that is composed of 5 highly skilled and committed professionals that integrate key competencies required to be a best-in-class radiopharmaceutical CDMO.

Tasks:

• Perform daily manufacturing and QC tasks thoroughly following CDMO and radioprotection procedures, including Environmental Monitoring.
• Support process developments and initial production batches for validation for Minerva regulatory approvals.
• Support chemistry development work for new metal-based tracers as per the Minerva project pipeline
• Support technical feasibility and optimization of radionuclide production.
• Support GMP compliance programs both for manufacturing and QC

Experience

• GMP radiopharmaceutical production (preferred)
• Radiometals, including nuclide production/purification and tracer labeling is an advantage.
• Analytical chemistry (e.g., HPLC, GC, ICP, radio-TLC) or isotope production.
• Writing GMP documents (preferred).

Qualifications:

• You have a background as a laboratory technician within radiopharmaceutical production or QC environments.
• You have a GMP mindset, allowing yourself to operate efficiently according to pre-established procedures.
• You have good problem-solving skills and a get-it-done/make-it-work attitude.
• You are an excellent team-player.
• You are eager to learn from peers and curious enough to make continuous improvement your “motto”.
• You are punctual and take pride in working with high quality – and you can also handle changes with a smile.
• You thrive in a fast-paced and service-oriented organization.
• You master English in writing and speaking (English is required, and Danish is an advantage).

Please submit your application by applying the link until April 10, 2023. The application must include a motivated cover letter and a CV addressing the listed qualifications. Applications will be evaluated continuously, and potential candidates will be invited for job interviews accordingly.

If you have questions regarding the position, please contact the Head of CDMO, Pablo Moreno, at pmo@minervaimaging.com

About Minerva Imaging
Minerva Imaging is a scientifically-driven CRO/CDMO founded in 2011, counting 130 employees. Our focus is on the use of advanced animal models within oncology and cardiovascular diseases and in vivo molecular imaging for translational research and drug development.

We engage with our collaborators to understand their scientific questions and discuss how our methods and capabilities can provide answers. We are rapidly growing, and the right candidate will be a key contributor to maintaining the scientific foundation and our approach to research while expanding our business. You will join a highly specialized CRO/CDMO with ambitions of taking disease treatment to the next generation of personalized medicines.

We are an informal organization that strongly focuses on open and honest communication. We value humor and natural care for one another, meaning stepping up and lending a helping hand to a colleague when needed.

We offer a combined compensation package that includes a base salary, pension, and an attractive bonus program. We care about our employees’ well-being and offer health insurance and a quality-conscious lunch scheme and arrange monthly social activities. Follow Minerva Imaging on LinkedIn for the latest news.

Click here to apply.