101 job matcher din søgning
Elsevier A/S, Aalborg
Pure is the world's leading research information system, used by research institutions across the globe. Pure is part of the Elsevier portfolio for institutional offerings.
We are seeking talented and self-motivated Software Engineers with skills in Java and a positive attitude to cross-functional teams. You will be joining an agile team in our office in Aalborg to help design, build, and maintain a world-class product.
You will be part of the Aalborg development hub, which focuses on developing Pure by expanding its capabilities to satisfy the increasing demand from research institutions throughout the world. Around 60 people are located at the Aalborg office, split into several engineering teams, with different focus areas.
- Follow best practices and apply software engineering principles at each stage of the development lifecycle.
- Write well-tested, documented and peer-reviewed code.
KAR+CO recruiting on behalf of Jupiter Bach A/S in Køge
The Group Controller is responsible for controlling of all group companies, monthly reporting, and reconciliations. Setting the stage and leading the process of optimizing the internal control environment and closing procedures in effort to ensure on time, high-quality financial reporting to the management.
The function will also include tasks within compliance, statutory reporting, taxes and transfer pricing.
Key responsibilities will include
- Controlling of subsidiaries to ensure valid accounting data across the group
- Implementing aligned group policies and procedures
- Participate in monthly consolidation and reporting activities
- Drive and ensure accurate month-end reconciliations for the Danish entities
- Contributing to the general development of financial management and reporting
- Ad hoc analyses and treasury tasks.
Do you want to improve the life experience for people with a hearing disability? Are you an Engineer passionate for technology? Do you also have a strong experience with real time embedded system development?
Your primary responsibility is to ensure the development of our embedded software mainly for Oticon Medical sound processors driving our implantable solutions.
There is a wide range of technical activities you will be involved in, but summed up, your main responsibilities can be divided into the following areas:
- Development and support of our current and future Embedded Software products
- Propose and innovate on embedded architectures to achieve our feature roadmap
- Use our medical SW development cycle, which complies with regulatory requirements, to implement, optimize, verify and document Embedded Software solutions
Maersk Oil, Esbjerg
You will lead the Tyra Future Project Procurement team and ensure flawless execution of all contract activities in full compliance with the project integrated schedule. As part of this, some of your key tasks will be:
- Actively participate and contribute to the Project Leadership team, accountable for all contract and procurement activities
- Develop tender strategies, recommendation to awards and contract management plans
- Manage major tenders and lead negotiations
As a member of the Tyra Future team, you are expected to be actively involved and support the HSSE plans and programmes. You will also be expected to personally role model ‘Incident Free’ values through your actions and behaviour.
Are you passionate about Business analytics and ready to implement and drive oversight of budgets and business KPIs across selected vendors, used by Medical & Regulatory Science (MRS) an R&D at H. Lundbeck A/S?
As our Business Analyst, you will ensure development, implementation and continuous improvements of appropriate budget and business KPIs models, processes and tools needed to ensure daily oversight of operations and maintenance. You will play a key role in planning, organizing and executing all phases of the tasks from start up to finish. Your work will typically involve working in corporate financial systems, SharePoint, Excel and Power Point.
LEO Pharma, Ballerup
Are YOU ready for a career change? Perhaps you are currently working as a nurse at a University Hospital involved in clinical trials or at a GP office and you would like to work in the Pharma Industry? Or you are working in Pharmacovigilance (e.g. as Drug Safety Associate) and would like to change into the clinical trial area?
As Clinical Data Manager you will be responsible for accurate, timely and consistent clinical data. You will provide clinical data management support to cross functional trial teams. You will have the opportunity to work with world-wide:
- Phase I trials: First-in-man trials
- Phase II trials: Dose-finding trials
Scalepoint Technologies, Copenhagen
Do you want to take part in developing the leading SaaS solution to the insurance industry in Europe?
As an IT Infrastructure Specialist you are taking part in our IT Operations Team which is responsible for our Hybrid-Cloud Infrastructure Setup. You are responsible for designing and implementing IT infrastructure which supports our business strategic goals. You take part in the response team.
You will join World Class IT Operations Team which enjoys of working in challenging and inspiring environment. We are working with a lot of fun. We are the team where everybody is willing to help others
Symphogen A/S, Ballerup
Symphogen is currently experiencing an increase in activities within both the early and late stage projects. Furthermore, Symphogen is planning to start phase III clinical trials and to apply for a Manufacturing and Import Authorization (§39 Licence).
Symphogen therefore plans to strengthen the QA organization with a Quality Manager.
As Quality Manager you will be involved in every step of the manufacturing process from generation of cell banks, upstream and downstream processes, final formulation, filling, analysis and release of the final drug product. The manufacturing is outsourced to various CMO's in EU and US.
The Quality Manager will participate for the quality group in our projects covering process and analytical validation, PPQ, clinical supply, and eventually marketing application.
Novo Nordisk A/S, Søborg
Are you motivated by setting up and driving global clinical programmes and do you want to exert your influence by leading project teams to develop haemophilia treatments? Do you thrive by working in an international environment and are you prepared to join an area with a high level of awareness and attention? Then we may have just the right job for you.
As a CPM, you are responsible for directing and co-driving one or more global clinical programme from an operational perspective. Currently, the department has several projects ranging from pre-clinical stages through marketed products. You will ensure that project key deliverables are met timely at a high quality and within budget by applying your project leadership as well as extensive operational Trial Management (TM) knowledge.
Novo Nordisk A/S, Bagsværd
Do you want to contribute to the safety and quality of Novo Nordisk clinical development? Do you have the competence and the medical knowledge it takes to handle adverse events reported from clinical trials? Would you enjoy being a key player in making sure that global regulatory requirements are met? Then you might be one of the Clinical Safety Associates we are looking for.
In order to ensure that global regulatory requirements are met, you will play a defining role in handling serious adverse events reported from our clinical trials. You will make sure that the individual adverse event reports are accurately and consistently registered and evaluated in our database and assess the need of requesting missing or follow up information on the reported events.
Dansk Supermarked, Brabrand
Take the first step towards a challenging career in a business driven IT organisation
Dansk Supermarked Group is on an exciting journey developing the retail sector of tomorrow. To support and drive this business transformation, we need skilled and ambitious graduates capable of and willing to grow with us. Becoming an IT Graduate with us means joining a professional and business driven IT organisation in an international company focused on growth.
We offer you an international platform for professional and personal growth, where you will get a solid foundation to build an ambitious career. With your potential and our support our goal is to turn you into one of our future Process Experts, Solution Experts or Project Managers within IT. Alternatively your knowledge and understanding of the DSG Business processes might open up challenging options in another part of our company.
The position is based in our central office in Copenhagen and reports directly to the Group Commercial PMO Manager. You will help with the administration of our NPD management system and assist the PMO team with a wide range of activities to ensure we are innovating effectively and efficiently.
- Assist in the day-to-day administration of our Carlsberg NPD management platform
- Support global and local project managers on e.g. governance related questions and technical issues
- Work together with project managers to ensure compliance to our stage-gate model
Ever wondered what's behind the curtain when you check in your luggage at the airport? Or how your delivery from Amazon can get to your door within 48 hours? Join our team and become an important player in the development of "mission critical" systems bringing together machines, technology and software.
BEUMER Group A/S in Aarhus is growing and we need new talented JAVA and/or C# developers for our SW Department. You will step into a large software organization of 125 skilled colleagues – with numerous facets in software development and IT hardware. The job will provide plenty of opportunity for your professional development, by going in the direction of software architecture, by specializing in specific components or by going into project management.
Take a look inside here!
Vattenfall A/S, Kolding or Hamburg
Do you want to make a real difference? We are looking for the right person to fill the position as Project Optimisation Lead
Vattenfall´s Business Area Wind is now recruiting a Project Optimisation Lead to be part of the VKF Team (Vesterhavs & Kriegers Flak offshore wind farms). The project is responsible for the safe and timely installation and commissioning of Vattenfall’s offshore wind farms.
The role as Project Optimisation Lead will be a first step into the growing Vattenfall Offshore Wind business and the right candidate will have the opportunity to support our growth taking on similar responsibilities. The Project Optimisation Lead will be preferably located in the Hamburg, or Kolding office, with regular travel between the two; must be flexible for occasional trips around in the northern part of Europe. If required you will also be expected to work on other projects across our offshore portfolio.
As specialist in the Section of In Vitro studies you will join a group of one academic (Head of Section) and three experienced technicians to deliver in vitro toxicological support to early discovery projects. As an expert in in vitro methods and/or molecular toxicology we envisage that you will actively take part in developing and optimising our current high content screening methods and propose new in vitro and/or in silico screening strategies, when relevant.
A very exciting and dynamic research environment with experienced, collaborative colleagues. We are dedicated in our work and take pride in delivering high quality results and safety assessments that support research projects in the best possible way. The working atmosphere is informal and positive, offering good opportunities for collaboration and personal development.
Novo Nordisk A/S, Kalundborg
Do you have experience with inventory management of technical components? Have you worked with procurement and quality control of spare parts in a GMP environment? Will you ensure that our production receives the correct components in compliance with all requirements? Can you establish an effective and agile inventory operation, aligned with key business goals? Then you are the new supply chain professional we are looking for!
You will set up the system that ensures correct spare parts for our production. You will be responsible for the total supply chain all the way from capturing requirements, to quality control and release for use. This includes registration of requirements to spare parts, negotiation with suppliers, purchasing, quality control of incoming goods and documentation, registrations in SAP PM/MM and general inventory management.
Semco Maritime A/S, Esbjerg
“Motiveres du af et dynamisk produktionsmiljø, som konstant udfordres på at levere kvalitet til aftalt pris i et marked, som er under pres for at få omkostningerne ned? Så søg jobbet her….” - Torben Thorhauge, Manager Fabrication Projects.
Som Project Leader vil du arbejde selvstændigt med ansvaret for små og mellemstore projekter.
Stillingen som Project Leader fordrer skarpe projektledere, som eksekverer til aftalt kvalitet, pris og tid. Du vil arbejde selvstændigt og til tider være en del af et større projektteam.
Vi tilbyder en meget udfordrende stilling i et dynamisk marked, hvor dine udviklingsmuligheder er store, når du leverer varen og skaber resultater. Der tilbydes en god lønpakke som matcher dine kompetencer og din erfaring.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen or Utrecht
Strong Project Manager to lead cross-functional early stage antibody product development
In order to strengthen the Project Management team, Genmab is looking for an experienced Compound Development Team Leader (CDTL) who will be based in Copenhagen or Utrecht.
As CDTL at Genmab, you will provide leadership to cross-functional international project teams. You will report to the Vice President, Project Management and to the Senior Director, Operations and Resource Management.
As CDTL you will :
- Develop and execute the project strategy for early stage antibody development projects from clinical candidate selection up to and including first human trials.
- Lead Compound Development Teams (CDTs) for two to three (co development) projects at different stages.
Novo Nordisk A/S, Bagsværd
Do you want to be part of a high performing team in one of the world’s leading pharmaceutical companies? Then you might be the right person for Novo Nordisk, as we are currently searching for an enthusiastic Corporate Counsel to be part of the Pharma Law team.
We offer an exciting and challenging position as Corporate Counsel, with a key focus on the following tasks: reviewing, drafting and negotiating complex contracts and related documentation, especially in in relation to outsourcing of clinical trials but also within other areas; maintaining and revising global corporate contract templates; participating in cross-functional working groups and providing legal advice to our key business stakeholders, primarily Global Development and Regulatory Affairs; preparing and providing training, guidelines and tools to our global legal and business stakeholders; driving ad hoc strategic projects.
Hansen Toft A/S søger for EDC Gruppen a/s på Frederiksberg
Ambitiøs projektleder, konsulent eller forretningsudvikler, der ønsker at drive onlineprojekter i en dynamisk branche og få det fulde projektlederansvar fra idé til leverance
EDC er inde i en spændende udvikling og som følge af en forandringsproces med flere større IT-projekter undervejs, ønsker virksomheden at ansætte en handlekraftig projektleder, der kan tage ejerskab og sikre professionel levering og eksekvering af udvalgte onlineprojekter.
Med reference til CIO får du det overordnede ansvar for en portefølje af projekter, hvor din hovedopgave bliver at styre og løbende følge op på scope, kvalitet, ressourcer, omkostninger og risici. Lige så vigtigt bliver det at sikre en god dynamik om teamets medarbejdere samt en effektiv kommunikation mellem forretningen og teamet, herunder forventningsafstemning om prioriteter med interessenterne i projekterne.