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Compass Human Resources Group A/S recruiting on behalf of Y-mAbs Therapeutics A/S in Hørsholm
Y-mAbs Therapeutics A/S is a late-stage clinical biopharmaceutical company focused on the development and commercialization of novel antibody-based therapeutic products for the treatment of cancer.
As CMC Project Manager for Y-mAbs, you will get the opportunity to contribute to state of the art research and be a part of a fantastic journey. With direct report to SVP Technical Operations, you will manage, coordinate and drive the chemistry, manufacturing and control part of projects in early and late stage development with specific focus on analytical and stability issues.
Also, the coordination of development activities within drug product formulation, assay development, control strategies, and quality control using external vendors together with writing and reviewing the technical content of the regulatory documents for submissions will be some of your tasks.
Would you like to use your bioinformatics skills within the area of depression research? Are you fascinated by working with large data sets and combining different types of data to gain new knowledge? Then we offer a 3-year Ph.D scholarship as a collaboration between the Bioinformatics Department at H. Lundbeck A/S and the Section for Computational and RNA Biology, Department of Biology, University of Copenhagen.
As a Ph.D candidate, your task is to analyze and combine these data in order to expand our knowledge about depression and patient subgroups. This will include using existing tools and developing new methods as needed. You will be collaborating closely with both bioinformatics and clinical experts at Lundbeck and University of Copenhagen. You will be expected to present your results both internally, at international meetings and in scientific publications.
Arla Foods, Viby J.
Are you ready to use your expert knowledge of how nutritional components affects the human physiology and biochemistry?
As Nutrition Scientist in the commercial business unit, “Health and Performance”, your work will focus on collecting, communicating and creating scientific documentation for the health effects of our ingredients for use in medical nutrition products. It will be your responsibility to manage a series of clinical trials within this area, and you will be overall accountable for securing the nutrition science evidence base supporting our ingredients.
Moreover, you are an essential part of the development of sales and marketing material and provide input to the development of new ingredients. As such, you also contribute to fuelling our ingredient pipeline with innovative ideas and a basis of valid knowledge for the further development of new products.
The successful candidate will become the Personal Assistant for the Integrated Operations Leader, Nutrition and Health.
In this role, you will work closely with and for the Integrated Operations Leader with a multitude of different tasks. The Global Integrated Operations Organization covers Manufacturing, Supply Chain, Planning and Logistics, SHEQS, Engineering, Lean/Six Sigma, Continuous Improvement for more than 50 sites.
- Heading the communication internally in the Integrated Operations organization globally
- Managing the agenda and travels of the Leader of Integrated Operations
- Arranging global meetings for Integrated Operations
Fontibus HR ApS recruiting on behalf of Amgen in Hellerup and Søborg
First - We trust that you are motivated by the Amgen mission of serving patients?
Also, we hope that you would like to join a professional, respected and growing biotech company with about 45 employees in Denmark and about 19.000 employees globally? If this resonances with you, then you are very welcome to consider joining Amgen, the world’s largest pure play biotechnology company.
The Human Resources Manager position is “a single contributor role”, and thus a board HR Role where you will be the HR point-of-contact in Denmark, the first local HR resource as well as a role where you within 6-12 months will be taking on additional HR Responsibilities/Projects within the Nordic-Baltic Region.
You will be based in Denmark, part of the Nordic-Baltic HR Team of 3 HR Professionals who are working out of Stockholm.
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to be part of a great, growing team responsible for global safety surveillance of Ferring’s portfolio within reproductive health and gastroenterology? Do you thrive in an international environment of great change where you can influence the surroundings? Do you like to work both with post-marketing and clinical activities?
We are looking for a permanent, experienced Pharmacovigilance Manager with good drive and positive energy.
As Senior Pharmacovigilance Manager you will play an important role in leading drug safety for a key area of Ferring’s portfolio working as an integrated member of a highly motivated and dedicated team collaborating with clinical development, regulatory affairs, affiliates and partners for assigned products/projects.
LEO Pharma, Ballerup
You can look forward to unfolding your skills in an international environment among truly passionate and talented colleagues and partners. You will become the team’s primary responsible for establishing design requirements in a systematic way and translating these into specifications – while ensuring design control all the way to verification and validation. You will focus on connectivity in order to capture data related to the use of LEO Pharma’s products, injection devices as well as lotions. You will:
- Develop cutting edge products within digital healthcare – combining HW and SW
- Translate requirements into specifications
- Ensure design control and create technical documentation all the way to verification and validation – aligned with our quality management system
Novartis Healthcare A/S, Copenhagen
Do you want to work for a Global Pharmaceutical company where you will be recognized for your contribution and commitment? Look no further, apply today for Head Market Access & External Affairs Denmark.
The Head Market Access & External Affairs Denmark (MAX & EA) has overall responsibility for securing market access of Novartis’ oncology products in Denmark. He or she leverages on a deep understanding of Danish political environment, healthcare structure and regulations to devise innovative MAX & EA initiatives that will provide a sustainable competitive advantage in a given business environment.
The Head MAX & EA Denmark ensures patient access to Novartis’ pharmaceuticals and therapies, and in collaboration with other functions influences and develops health political legislation, regulations and reimbursement systems.
Ferring Pharmaceuticals A/S, Copenhagen
Your main focus is to work within the device development projects as responsible for the design controls from project initiation until successful design verification, validation and transfer. The position is an opportunity to contribute to the development and documentation aspects of the device part of drug delivery projects including responsibility for the risk management activities, as they move from project initiation to clinical studies, manufacturing, global submission and commercialization.
Your main responsibilities will be:
- Structure and execute on design documentation as defined in development plans for projects across therapeutic areas. This includes collaboration with external development partners
- Structure and execute risk management documentation (plan, analysis & summaries)
- Setup review for documentation and secure stakeholder involvement underway
Til Commercial Packaging søger vi dedikerede og dygtige operatører til nathold hurtigst muligt. Commercial & Clinical Packaging er en del af Lundbecks farmaceutiske produktion, og vi er pt. 70 engagerede kollegaer fordelt på 6 team af operatører, support og ledelse.
Du vil få base i Commercial Packaging, i et team på 11/12 dedikerede kollegaer fordelt på 3 skift, der har ansvaret for en pakkelinje til pakning af tabletter i blisterkort og karton. Der arbejdes under GMP regler og jobbet består hovedsageligt i maskinbetjening, maskinoptimering, proceskontrol, omstilling, rengøring og løbende dokumentation af disse aktiviteter. Opgaverne løses i tæt samarbejde med dine kollegaer.
Widex A/S, Lynge
The Applied Research team is part of the Audiology department. Our core areas of work are within audiology and the application of audiological test methods. We support the R&D department by validating concepts, features, and products, with the aim of guiding the development of new hearing aids and apps. We use our knowledge of audiology to ensure that our products are as meaningful and useful as possible for our customers.
The main tasks and areas of responsibility are:
- Applying audiology and hearing science expertise in the evaluation of new hearing solutions.
- Experiment design and execution.
- Statistics, both on own projects and as sparring for the group.
Novo Nordisk A/S, Bagsværd
Maternity covers in Global Safety as a Senior Safety Surveillance Adviser (Biopharm) and a Safety Surveillance Adviser (GLP-1) are open for hire from July and August 2018 respectively.
Would you like to be part of an organisation of highly talented pharmacovigilance professionals? Are you naturally curious and analytical? Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? Then you may be our new colleague in Global Safety.
In the positions you will be responsible independently or together with colleagues for the ongoing safety surveillance of one or more of our products. Key responsibilities include analysis of safety data (e.g. potential side effects), medical evaluation of safety information received from sites participating in our clinical trials, or from patients or prescribers using a marketed product.
Novo Nordisk A/S, Bagsværd
Are you looking for an opportunity to work in drug safety and use your skills as a scientific communicator? Do you build strong relationships with stakeholders and enjoy putting plans into action? Join us as a Safety Medical Writer and use your skills to ensure patient safety and best practice.
As a Safety Medical Writer in Safety Surveillance Reporting at Novo Nordisk, you will be responsible for planning and managing document preparation of Development Safety Update Reports [DSURs], Periodic Safety Update Reports [PSURs] and Clinical Risk Management Plans [RMPs] in a cross-functional environment and ensuring high quality scientific writing.
You will work in close collaboration with Safety Surveillance Advisers, Medical Specialists from Global Development, Medical Advisers from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers.
Ambu A/S, Ballerup
Are you looking for independence in your job and a working day characterised by exciting new challenges? Would you like to be part of Ambu’s new product development groups and ensure that we meet all regulatory requirements? And are you looking for an international job? Then Ambu might be your next career move…
As Senior Regulatory Affairs Professional, you will be responsible for ensuring compliance with regulatory requirements for products and processes.
Your primary responsibilities will be to:
- Participate in development projects as a regulatory professional sparring partner.
- Contribute to Ambu successfully implementing new EU medical device regulations.
- Have fully updated knowledge about regulatory requirements.
The iLoop (Iterative Cell Factory Development Loop) Core section at The Novo Nordisk Foundation Center for Biosustainability (DTU Biosustain) is a translational research unit focused on microbial cell factory engineering.
As part of the design-build-test cycle operated in the iLoop, the generation of relevant analytical data constitutes an important part of the test and design phases of cell factory engineering. In particular, mass-spectrometry data can be helpful in elucidating the internal state of engineered cells.
We seek a highly motivated PhD student to apply modern machine learning methods to the analysis of metabolomics data. Specific application areas will include raw mass-spectrometry data processing, compound identification, and biomarker elucidation.
3Shape A/S, Copenhagen
Are you an experienced Product Marketeer and love to commercialize products that change the work-life of your customers – products that helps our customer provide better treatment for their patients? Are you looking to develop yourself and your colleagues and achieve ambitious goals?
As Product Marketing Manager, you will have the following responsibilities:
- Launch new products in the market place and ensure organizational readiness to maximize commercial success
- Responsible for the full product life-cycle commercial activities keeping the product top-of-mind with resellers, partners and end-users
- Contribute to product roadmaps working closely with product management
LEO Pharma, Ballerup
If you bring hands-on CRA experience backed by solid leadership skills within remote management as well as an open-minded and positive mindset, we have just the right job for you.
As Head of CRA’s you have two main objectives. One is to ensure high quality across the many trials conducted by your team in Region Europe. The other is to add our special ingredient “the LEO touch” in order to establish and maintain long-lasting and mutual beneficial relations to our partners/trial sites. You will be working out of LEO Pharma’s headquarters in Ballerup, Greater Copenhagen.
Your primary tasks will be to:
- Head a team of approx. 15 CRA’s across region Europe
- Be part of the leadership team in Trial Execution and contribute to setting the overall direction for the organization
- Ensure site recruitment aligned with recruitment targets
LEO Pharma, Ballerup
LEO Pharma has set the ambitious goal to become the world’s preferred dermatology care partner and to improve the quality of life for millions of patients around the world. To succeed, we invest massively in R&D. As a result, our pipeline and clinical activities are growing rapidly, and that is why we need you and all of your skills as leader, coach and guiding light within Trial Management.
As Head of Trial Management you will head one of two sister teams counting 10-15 Clinical Project Managers/Trial Managers, based at LEO Pharma’s headquarters in Ballerup, Greater Copenhagen. Your overall objective is to ensure high quality clinical trials delivered within agreed time and cost. Your primary tasks will be:
- Head a team of 10-15 Clinical Project Managers/Trial Managers
- Ensure high quality clinical trials within agreed time and cost
- Keep the total portfolio overview and allocate resources to ensure maximum efficiency
Systematic A/S, Aarhus
Vil du gerne gøre en forskel og være med til at udvikle den elektroniske patientjournal i Columna Clinical Information System? Har du erfaring med Java og Android? Så har vi jobbet til dig.
Som softwareudvikler på Columna CIS vil du arbejde tæt sammen med kunden og have mulighed for at gøre en forskel for alle brugere af systemet, dvs. læger og sygeplejersker. Du bliver en del af et agilt og selvkørende team med dygtige kolleger, hvor du vil være involveret i en bred vifte af udviklingsrelaterede opgaver. Du kommer til at arbejde med en lang række teknologier, herunder men ikke begrænset til Java EE, JBoss, SQL, Git og Teamcity.
Ambu A/S, Ballerup
Are you looking for a job with a high degree of influence and a varied working day? Do you want to be part of developing professional and safe medical devices? Moreover, do you have a high energy level?
As part of the Corporate Clinical Research & Biosafety department, you will work closely with Global Innovation teams, as well as Marketing teams, to develop medical devices.
In the job as Clinical Research Specialist/Medical Writer, your main responsibility will be to participate in product development projects, and to provide clinical and medical writing input to ensure safe and efficient devices.
You will be involved in all clinical and medical writing aspects of product development, including to:
- Prepare clinical documentation to support product approval
- Plan, coordinate, execute, and report pre-clinical activities, and clinical investigations