65 job matcher din søgning
Evaxion Biotech ApS, Copenhagen
You will be working across the drug discovery and development continuum supporting coordination and execution of preclinical experiments; you will be conducting mouse tumor studies and ex vivo analyses for immuno-oncology vaccine trial testing.
Your top priority will be to coordinate and assist on in vivo studies to assess anti-tumor responses of targeted immunogens and to conduct established immune assays to detect and quantitate immunological responses. You will participate in discussions with project leaders and experimental team concerning specific project-related data analysis and discuss future directions of projects.
- Conducting in vivo pharmacology studies and ex vivo immuno-profiling assays
- Ensuring scientifically correct and consistent experimental setup and analysis using state-of-the-art approaches
- Coordinating task between relevant team members
Chr. Hansen A/S, Hvidovre
Your focus area will be analytical QC methods giving performance results of the products as a part of the QC release. Different analytical technics as continuous measurement of pH, volatile compounds by GC (VOC), Spectrophotometry, Flowcytometry and others are currently used. Experience in Microbiology would be beneficial.
Expected travel days per year between 10-25 days.
Your primary responsibilities
- Drive and coordinate optimization projects (e.g. validation of methods, automation, improvement of sensibility and variability) on existing and new analytical methods across all QC laboratories
- Secure alignment of analytical methods and procedures across all QC laboratories
- Managing and facilitating global analytical QC networks
We are opening 2 newly established positions as Project Managers to strengthen our project management within RD Portfolio Management and Global Project Leadership. We manage all global development programs through a strong matrix organisation.
You will refer to the Global Project Lead. Your role is to ensure that the project progression is executed according to the global project strategy and plan. You will work closely with the GPL and line of business to ensure alignment and execution of plans.
Your primary responsibilities will include project planning and management, tracking of critical issues, tracking of timelines, tracking of project goals and deliverables, risk management, monthly reporting, meeting planning, presentation preparation, as well as driving the overall project forward by various ad hoc-tasks.
A typical work week is usually booked some weeks in advance and you spend Monday to Thursday at customers’ sites typically working with preventive maintenance and validation. It is normally a day’s work or 2 per visit if you are travelling. As a true Field Service Engineer, you like to have an eye on your e-mail and phone to make sure you can respond quickly and fit in another visit at a nearby site if your schedule allows it.
- Become technically proficient in the support of our Biologics, BioResearch, Drug Discovery and Imaging products so that you can provide consistent, world class levels of service and support to our customers
- Take ownership of all assigned customer service calls including repairs, installations, preventative maintenance and operational qualification schedules and ensure timely closure of outstanding service issues
LEO Pharma, Ballerup
Do you want to work with drug safety in clinical development?
As Senior Safety Advisor you will be a key player in the safety surveillance and development of one of LEO Pharma’s new biologics Tralokinumab for the treatment of atopic dermatitis.
We are offering a job with considerable individual responsibility, challenges, and the opportunity to develop your professional and personal competencies. As Senior Safety Advisor, your main focus is to be globally responsible for effective safety risk management processes with main tasks being:
- Signal detection and management
- Participation in clinical trial teams providing safety input to clinical development discussions and documents, e.g. trial protocols and Investigator’s Brochure
- Preparation of safety input to various regulatory documents
Xellia Pharmaceuticals ApS, Copenhagen
Do you want to take the lead in order to ensure the highest quality processes on a daily basis?
At Xellia, you will step into an internationally growing company with good development opportunities. You will be able to influence the business and be part of an entrepreneurial and successful organization owned by Novo Holding A/S.
As our new Manager MQA API, we will promise you an exciting and challenging position where you will contribute to the running and managing of MQA API in a cost-efficient manner. You will be budget responsible, which includes having to follow up on the department’s expenses.
Carlsberg Breweries A/S, Copenhagen
The Carlsberg Research Laboratory is looking for a Beverage Technician to strengthen our New Ingredients Platform. As a technician, you will join an experienced international team of technicians and scientists and work in a dynamic research environment. You will be part of a world leading global company with outstanding research facilities.
- Support beverage development projects and other activities within the New Ingredients Platform.
- Conduct laboratory/small scale beverage development trials in conjunction with scientists.
- Conduct small scale (laboratory) fermentation / brewing trials in conjunction with brewing scientists.
Genmab A/S, Copenhagen
The Drug Supply Manager will be responsible for managing outsourcing of packaging, labelling and distribution of clinical trial supplies for early as well as late stage Genmab clinical trials. Moving forward with many late stage trials in pipeline, the Drug Supply Manager will also assist in implementing IRT and integration to other systems.
Key responsibilities will be but not limited to:
- Manage and coordinate drug supply and to provide IMP for clinical trials
- Manage and coordinate ancillaries, pre-medication and comparators for clinical trials
- Implementing IRT and integration to other systems e.g. eCRF for trials
Genmab A/S, Copenhagen
Genmab is looking for an experienced CMC Regulatory Specialist to strengthen the Regulatory Affairs team in Copenhagen.
Genmab is an international biotechnology company specializing in the invention and development of differentiated human antibody therapeutics for the treatment of cancer and other important human diseases.
As RA Specialist at Genmab, you will be responsible for operational and strategic regulatory input on CMC matters to support worldwide development and commercialization.
You will be part of the operational teams directing and coordinating international regulatory submissions supporting the conduct of the clinical trials. You will be part of a team of 9 reporting to VP, Head of Global Regulatory Affairs.
Ferring Pharmaceuticals A/S, Copenhagen
Do you want to make your mark as part of a very well functioning specialist team?
If your field of expertise is clinical operational processes and you are looking for an opportunity to make a difference clearly above the average, this job is your perfect match. In this newly established position you will play a pivotal role in our efforts to take Ferring to the next level within smart and intuitive use of processes and systems to ensure global clinical compliance. Influence and impact are guaranteed just as help and positive knowledge sharing in our very well-functioning team.
Basically, your focus as Process & Systems Specialist is to help your colleagues across the global organisation to “work smarter, not harder”. You will do so by unfolding your skills on two parallel tracks: On one track, you will develop and optimise clinical operational processes handled in clinical operational systems.
Radiometer Medical ApS, Brønshøj
The role includes responsibility for both Upstream and Downstream Marketing activities. As such, the Product Manager is responsible for the daily product management activities around commercialization of the TC products and for defining features of the future TC monitors.
The TC Product Management team consists of two Global Product Managers responsible for both upstream and downstream Marketing activities. The Global Product Manager is responsible for his/her own product areas and collaborates with the other Product Manager in promoting the overall TC solution. In addition, the candidate interacts with many other functions in the Radiometers headquarter (e.g. Marcom, Clinical and Scientific Affairs, R&D, Regulatory Affairs) as well as with our subsidiaries worldwide.
LEO Pharma, Ballerup
Do you want to be part of the Global Bio-Dermatology marketing team working with LEOs first biologic?
You will be part of the global Bio-Dermatology team within LEO in Denmark. The team consists of dedicated experts who all share the common goal, passion and dedication of launching the first biologic in psoriasis for LEO Pharma. As part of this team you will report to the Senior Director in the Global Bio-Dermatology team.
Your job as a Global Senior Brand Manager (Global Senior Patient Solution Manager) is to drive/develop and implement all branded communication for our first biologic, Kyntheum® (including MCM (Multi Channel Marketing)). An important task is to continue develop and shape brand differentiation through innovative initiatives with thorough market insights.
Cirqle Biomedical Contraception IVS, Copenhagen
Cirqle Biomedical is seeking a talented scientist to take part in the development of a groundbreaking non-hormonal contraceptive for women.
As a R&D scientist you will be an essential driver of the scientific discoveries that will translate into commercially successful products. You will be conducting pre-clinical research with a network of researchers in and outside Denmark and report directly to the CSO. We provide both a competitive salary and attractive compensation in company shares.
- Perform scientific experiments and generate data to support the development of the product
- Analyse and present data to the management team
- Produce documentation of protocols, procedures and results
Danmarks Tekniske Universitet, Kongens Lyngby
DTU Biosustain announces a vacancy in the Bacterial Signal Transduction group headed by Professor Ivan Mijakovic. The focus of our research in this domain is the production of green metallic nanoparticles by microorganisms. We seek to generate functionalized metallic nanoparticles that will be optimized for medical applications, e.g. treatment of cancer, inflammations, biofilm problems etc.
The research field of the position is within the area of green nanoparticles production, characterization and their medical applications. The production will be carried out in the model organisms such as B. subtilis, E. coli or other strains enhanced via genetic engineering to produce well-defined metallic nanoparticles.
Samplix ApS, Herlev
We are seeking a Sales Development Manager, Nordics to bring novel, advanced products and technology for genetic analysis on single DNA molecules to the market in the area of next generation sequencing
Do you want to be a part of an interdisciplinary dynamic team who shares the vision of better healthcare by improving next generation sequencing and securing the integrity of DNA information?
We are looking for an experienced and highly motivated Sales Development Manager for the Nordic countries. You have strong technical knowledge in the area of next generation sequencing with credibility to effectively consult on solutions, products and technologies with key decision makers. You are excited to work with a dynamic team of talented professionals to introduce and grow the Xdrop™ technology and products in your region.
Immudex ApS, Copenhagen
Immudex is looking for a Sales Territory Manager for the territory of Europe to cover a twelve months maternity leave.
We are looking for a Sales Territory Manager with a deep knowledge of immunology/immune monitoring to be our European customer facing lead, leveraging scientific understanding of immunology in a commercial role.
- Work proactively to maintain and grow the European Customer base by
- managing sales process for customers within the territory incl. responding to customer enquiries
- performing visits to and telecom calls with customers to establish optimal solutions for their technical challenges and applications of Immudex’ products
- identifying and developing new accounts and sales opportunities.
LEO Pharma, Ballerup
Do you have a background within inflammation or dermatology? And a passionate interest in using your strong protein and molecular biology knowledge to build in vitro biological & biophysical assays for screening and characterizing new compounds to help bring new treatments to skin disease patients? Then you could be our new colleague in the In vitro Biology department.
We are looking for a scientist to join us for a 2-year position. You will be working within early pipeline projects, towards the common goal of identifying new compounds that target pathways involved in the pathogenesis of inflammatory skin diseases. Using your expertise within techniques such as SPR, HTRF, and endogenous tagging technologies, you will set up assays to analyze protein-protein interactions and molecular events – enabling project progress.
Antimicrobial resistance (AMR) is among the biggest challenges for human and animal health. If global drivers of this could be identified we might perform interventions at a much earlier stage.
We are seeking a candidate for a vacant postdoc position in epidemiology within the area of global surveillance and predictive epidemiological modelling of infectious diseases with a focus on antimicrobial resistance (AMR).
You will be affiliated with the Genomic Epidemiology Research Group, which primary task is to conduct targeted research with the aim of predicting and preventing infectious diseases in humans and animals, and supporting global detection, surveillance and control.
GEA Process Engineering A/S, Søborg
As part of the growth plan for the Service business, GEA is seeking a Service Product Manager for the Application Dairy, Food and Beverage.
You will be responsible for a global service product portfolio and the product development process within that portfolio from idea generation to commercialisation. The portfolio will be linked to customer applications as well as technologies. Time-to-market is crucial and you will ensure that key challenges in the supply-chain are addressed in the development. You will further develop and optimize products that are already introduced to the market.
- Product management of application portfolio Dairy, Food and Beverage.
- Ensure that GEA have the full needed product portfolio for a strong service business
- Project management including planning, budgeting, resource management
We are looking for an experienced academic who will provide scientific and project management leadership for analytical development activities.
Joining us, you will be part of an organization which is solely focused on development of new drug candidates for brain diseases, and you will be part of the Chemical and Pharmaceutical Research (CPR) area which is responsible for CMC development at Lundbeck.
You will be responsible for the analytical development in our global development projects and coordinate the CMC analytical input for clinical studies. You use your experience within API analyses to drive the discussions and internal procedures covering fate and purge of API impurities, and the corresponding regulatory documentation.