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Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Senior Regulatory Affairs Manager

This pivotal role will involve navigating the complex regulatory landscape associated with technologies for the production of hydrogen, its derivatives and other related technologies. This critical role will also involve ensuring compliance and strategically influencing regulatory development to support our mission.

The ideal candidate will have a deep understanding of energy regulations, a passion for sustainability, and the expertise to guide our company through the evolving regulatory environment.

Science Lab Technician

Are you the lab wiz that will support our science teachers in making science the new favourite at CIS?

You will be providing technical support for our laboratory facilities including ensuring that our teachers and students have the right equipment for their lessons and that the lab environment is clean, safe and well-stocked in-line with Health and Safety requirements.

You probably have a background in the sciences and can cover science classes in the event of teacher absence.

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

Operations Data Coordinator for Drug Substance Production

The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.

You will be part of a team with a great sense of humor and a high willingness to support where needed.

Lab Quality Coordinator, GCLP Laboratory

As Documentation Coordinator at the laboratory in Lund at MinervaX, you will play a central role in the establishment of a GCLP laboratory for clinical samples from MinervaX’s prophylactic vaccine targeting Group B Streptococcus (GBS). The GLCP laboratory is established to move into phase III clinical trials. You will be responsible for the writing, coordination, storage, and maintenance of documentation in the whole laboratory area.

This is a unique opportunity to join the journey into building a GLCP compliant laboratory. As this is a new position you can develop this role according to your own ambitions and will be primary person on documentation support.

QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Research Analyst

Are you in the right job? Do you want a challenge out of the ordinary?

The Primary Research Analyst has the responsibility of identifying, developing, and maintaining a network of contacts and relationships in the pharmaceutical and biotech industry and organizations.

An academic background in pharmacy or in biotechnology is an advantage but not a necessity as extensive internal training will be provided.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

Sales Manager

Are you seeking to make a difference in an innovative, fast growing medtech company with a cutting-edge technology? We're currently seeking a dedicated individual to fill a position as Sales Manager.

Your main responsibilities

• Lead generation
• Develop and execute sales strategies
• Customer relationship management

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.