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Clinical Supply IRT/RTSM Specialist
Come help us deliver high-quality clinical trial supply to trials all over the world
We are looking for an IRT/RTSM specialist to help us ensure timely setup of IRT/RTSM systems to support the delivery of trial supply for Ferring clinical programs globally.
In this role you are expected to not only collaborate closely with cross-functional teams but also contribute to a knowledge-sharing mindset and promote a collaborative and innovative work environment. You must have a flair for respectful communication with a range of stakeholders such as Clinical Operations, IT and Quality Assurance.
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.
Senior Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.
Lab Maintenance Technician
We are looking for a Lab Maintenance Technician for our client’s brand-new semiconductor and fabrication laboratory in Copenhagen.
The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.
As a Lab Maintenance Technician, you will play a crucial role in making sure that the Lab is operational, and that equipment always is performing accordingly.
Senior Research Technician
Do you want to work with data and HPLC analysis?
You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.
Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:
- Perform analytical method development in close collaboration with the responsible scientists
- Support formulation development studies with analyses
Senior Research Technician
Do you want to use your experience and problem-solving skills to work with pharmaceutical product development and early-stage development with a focus on characterization (MFI, DSC, HPLC)?
As a senior research technician, you will spend most of your time in the lab, where your primary role will be to prepare, plan, and perform pharmaceutical development work, including stability studies.
Column Pack Operator
The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, our teams and looking for passionate, mission-driven people who want to make a real difference in people’s lives.
We are currently looking for candidates to work within Drug Substance Manufacturing (DSM) Support and become part of a newly established team, responsible for preparation, packing and qualification of chromatography columns.
Clinical Trial Assistant
Are you looking for the possibility to unfold your competences within clinical operations even further? Do you thrive in an innovative environment working alongside dedicated clinical research professionals? Are you a self-driven team player, who enjoys a varied and influential day at work?
Pharmacosmos A/S is a progressive and innovative pharmaceutical company with headquarters in Holbæk, Denmark. We are on an exciting journey of global growth inventing new and innovative treatments, and right now we are expanding our team with a Clinical Trial Assistant.
SAP Master Data Specialist
Do you want to be a part of Process Support in a company with a unique impact on global healthcare?
You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.
Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Biocompatibility Specialist
We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.
This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.
Creative Assistant
Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?
Your Focus will be:
- Always following correct compounding procedures
- Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
- Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.
Application Technician – Food Ingredients
We are looking for an employee with an interest in laboratory and food technology to assist in the AKV FoodLab in Aarhus, where you will become part of the team.
Here you will play an important role in relation to taking part in the ongoing laboratory work with a confident and collaborative team approach.
As an Application Technician in AKV FoodLab, your primary tasks will consist of:
- To assist the Senior Application Specialist with research by running trials of a broad range of applications in the FoodLab and conducting analysis and characterization of food products.
- Maintenance and cleaning of process equipment.
- Contribute where required in purchasing tasks for the FoodLab.
Senior Regulatory Specialist
The Senior Regulatory Affairs Specialist at Radiometer is responsible for collecting and generating documentation for product submissions to ensure compliance with international regulations. This role is critical for ensuring that Radiometer's products can be sold in markets around the world.
If you thrive in a fast-paced environment, are used to playing a critical supporting role and want to work in a world-class efficient team that is part of a Global RA department and have interactions and stakeholders to connect with in a global scale - read on.
Health, Safety and Environment (HSE) Manager
Are you a seasoned Health & Safety professional seeking an opportunity to thrive in a supportive and dynamic environment?
We have an exciting opportunity to recruit a Health & Safety Manager, you will play a crucial role in maintaining and enhancing the safety standards at our facility. Your responsibilities will include designing training programs, conducting risk assessments, identifying, and controlling hazards.
Regulatory Affairs Manager
The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.
This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:
- Ensure regulatory compliance to maintain market approvals
- Lead a team of skilled RA associates
- Ensure alignment with relevant stakeholders
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 Supplier Quality Engineer
This is a key role within the Global Quality function, where you will have the objective of supporting the maintenance and improvement of ConvaTec’s Global Supplier Quality program and conducting supplier audits to ensure compliance.
Key Duties & Responsibilities
- Support and lead where appropriate, supplier selection, evaluation, and approval.
- Generate appropriate key performance indicators to assess supplier.
- Drive resolution of corrective actions.
Regulatory Affairs - Senior Specialist
Do you want to join an advanced biotech company that expands exponentially to develop and manufacture the leading biological products on the market today and for the future?
Equipment QC Professional
Would you like to work with complex problem solving, optimization and collaboration in an ambitious Good Manufacturing Practice (GMP) environment?
Development Scientist
Are you a skilled protein purification professional with a strong interest in optimization and support?