Do you want to be a key player in a high growth medical technology business? Are you passionate about developing and optimizing quality processes in a global organization? Do you want to have a positive impact on peoples’ lives? Do you want to grow and develop high performing teams?
in a biotech company focused on the discovery, design and development of innovative peptide-based medicines
in a biotech company focused on the discovery, design and development of innovative peptide-based medicines
In a biotech company focused on the discovery, design and development of innovative peptide-based medicines
An exciting opportunity has recently been created for a Sales Director at Mediq, and this might be the position for you!
PharmaRelations is now looking for a Head of Regulatory Services for Denmark who wants to build up and develop our In-House services within Quality Assurance, Regulatory Affairs, Pharmacovigilance and Medical Device in Denmark.
As Sr. Electronics Engineer you will join our System Engineering team, a cross-disciplinary team of 4-6 dedicated colleagues who has the overall responsibility for the entire ECGenius System. Your role will be to take responsibility for the electronics related tasks and design of the ECGenius System.
Do you want to be part of a highly competent Team when it comes to GxP and GAMP5 in relation to the delivery of automation and information projects to Life Science customers?
We are looking for a passionate Senior GCP/PV QA Manager, who will support the quality in Genmab’s promising product portfolio and promote GCP and safety compliance and continuous process improvement.
As Clinical Biometrics Oversight Lead, your overall objective is to support the operational excellence in Biometrics by supporting development of compliance, high-quality, and efficient processes and systems in collaboration with the relevant biometrics functions and other stakeholders across the organization as well as outside the organization
Join a clinical-stage and diversified pharmaceutical company focused on identifying, developing, and commercializing treatments for immunology and infectious diseases
Join a highly ambitious, transformative, and efficient biotechnology company that had 4 products ready for the market within only 4 years. c. Opslaget skal linke til stillingen på vores hjemmeside
Are you experienced in Regulatory CMC and are you able to drive and develop regulatory strategies for CMC activities? Then Symphogen is looking for you as their next member of the Global Regulatory Team!
Do you have a medical background, experience from designing trials and drug development programs and a track record in clinical research and science within gastro-intestinal, rare diseases or metabolic disease areas? Do you have the drive and the talent for leading a medical and scientific project team? Are you motivated by supporting, learning and collaborating?
The candidate will be part of a great team of three in the department; QA Computerized Systems which support the business with IT QA resources and GxP computerized system implementation and operation.
GSK Pharma is looking into several large launches in the nearest future across all their therapeutics areas and is now looking for an additionally colleague who can join and be a key member of the Market Access team who all works dedicated to secure access to GSK medicines through reimbursement and guidelines.
The quality area of Genmab is growing and looking for a new colleague to join the QA Department as Senior Manager, QA GMP.
Do you want to be part of driving CMC projects forward and coordinate the change portfolio for Lundbeck’s Biologics CMC projects and products?
Do you want to work in a production department in rapid development? Then you may be the technician we are looking for, to review and set for the release of produced batches of drug substance for ALK's tablet-based allergy vaccines.
Are you willing to challenge the status quo and embark on a transformational journey in a pharma company with an ambitious growth target in the years to come?
Would you like to have a key role in the clinical development in ALK and have the opportunity to influence the strategy on how to achieve the organizational goals of ALK?
Zealand Pharma A/S (Zealand) is looking for a CMC Submission Project Manager who is energized by working in close collaboration in teams on complex tasks with lots of fun and learnings.
The job includes execution and support to device development, device manufacturing and lifecycle management improvement projects for drug delivery devices.
As a Senior Teaching Fellow, do you want to help ensure more innovation in and future security of the Health Service?
An established leader in peptide innovation, our Medicinal Chemistry department in Copenhagen, is seeking a talented and motivated principal laboratory technologist to join our team.
Zealand Pharma A/S (Zealand) is a Copenhagen-based biotechnology company focused on the discovery and development of peptide-based medicines.
Exciting opportunity in a specialty biopharmaceutical company
Do you want to be part of a young organization and a team that is about to embark on an exciting journey to bring our IL-22 lead program to patients?
Are you experienced in testing of monoclonal antibodies, and do you want to push the boundaries of cancer treatment by applying your knowledge?
Our Medical team at Nykode are now looking for a Clinical Trial Manager! The Clinical Trial Manager (CTM) will be responsible for the overall planning, management, conduct and oversight of assigned clinical trials in Nykode.
A unique opening for a highly-skilled scientist for Antibody Engineering, Molecular Biology, and Drug Discovery
Exciting opportunity to lead safety assessment strategy during all non-clinical and clinical phases at Symphogen
Exciting opportunity to set your mark within Biomarkers at an innovative biotech company