125 job matcher din søgning
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
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.
Niels Brock International offers a bachelor’s degree in Business Administration at its Copenhagen campus. The bachelor’s degree program also has a partnership agreement with a university in China and a university in Vietnam in which Niels Brock offers the final year of its bachelor’s degree online. In addition, Niels Brock is the member of California International Business University, an American university that offers the same bachelor’s degree as Niels Brock and an MBA.
As the Academic and Compliance Officer, you will be required to complete the following activities:
- Overall responsible for all accreditation work at Niels Brock International and CIBU, San Diego.
- Lead and manage projects for the Compliance Committee, which consists of Executive Vice President, the Dean of Academic Affairs, Program Managers and the Dean of Student Affairs.
As Information Security Officer you will join PwC Network Information Security group (NIS), reporting to NIS Management in UK and have a dual reporting line to PwC Denmark.
You will support the PwC Denmark Firm in the development, implementation, maintenance and enhancement of all information security related activities in alignment with the Network Information Security Strategy and Policies.
You will influence and engage with the business and functions in all areas of information security, including security policies and standards, awareness, incident management, security consultancy, legal and regulatory compliance, security compliance audits and security budget.
Would you like to play a key role in transforming our international B2B business into delivering truly unique energy solutions and value propositions to our large commercial and industrial customer groups in Denmark, Sweden, Germany and the UK?
Join us and become a business analyst in our internal start-up, Energy as a Service, where you’ll be responsible for identifying new market opportunities and developing value propositions and bespoke solutions for our customers.
To be the frontrunner in the green energy transformation, we invest significantly in innovation and empower our employees to help shape the renewable energy technologies of the future. We cultivate a collaborative, dynamic and diverse work environment and encourage career-long learning and development so our people can realise their full potential.
Danske Bank, København
Er du interesseret i at forvandle ord til handling? Forvandle krav til løsninger?
Som analytiker skal du medvirke til sikre, at banken globalt lever op til såvel eksisterende som kommende regulatoriske krav på værdipapir- og derivathandelsområdet iht. MiFID II, EMIR, Short Selling, Dodd-Frank, SFTR, etc.
Du deltager i projektarbejde, tolker ny lovgivning og specificerer kravene til nye processer, procedurer, kontroller, rapporter og systemer/systemændringer. Inden for forskellige kontrolområder er du med til at udarbejde analyser, værktøjer, programmer, beregninger, etablere databaserede kontroller samt videreformidle og følge op på resultaterne. Du deltager i automatiseringen og strømliningen af det eksisterende kontrol-set up.
Maersk Oil, Esbjerg
The Lifting Authority is responsible for offshore rigging and lifting operations, ensuring the safety of personnel, integrity of equipment and improving operational practices. The position is an onshore role, where you provide support to both asset groups in Danish Business Unit.
If you like to set the standards? Then this role is the right one for you!
LEO Pharma, Ballerup
As a student assistant, you will be given a combination of recurring tasks as well as being included in one or more developments projects allowing you to help drive EU+ business. Tasks will be fine-tuned according to your profile but will broadly cover:
- Data input into SAP of budget and parallel trade data by country
- Data input for cluster Finance teams on an ad-hoc basis
What we can offer:
- As a student assistant in LEO Pharma you will gain insight and experience in an international pharmaceutical company and finance processes
- You will be working alongside the Finance Business Partner for EU+ and EU+ Regional Finance Director who will provide on the job training and deep insights into how Finance in industry work from over 40 years of experience between them
Er du grafiker med sans for detaljer i tekst og grafik, og trives du i et team med forskelligartede opgaver, så kan det være, at det er dig vi søger som Artwork Coordinator til afdelingen Artwork & Master Data.
I jobbet som Artwork Coordinator vil du blive trænet i udarbejdelse og vedligehold af artwork til pakkematerialer for hele Lundbecks produktportefølje i overensstemmelse med myndighedskrav og vores interne designmanual. Du vil få et tæt samarbejde med Regulatory Affairs, Pakkeriet og resten af Global Supply Chain, hvor vi har stor fokus på vores kunders behov og tilfredshed. Da Lundbeck opererer globalt både med hensyn til udvikling, produktion og salg, vil man ofte være i dialog med vores regulatoriske kontakter i udlandet og andre afdelinger på hovedkontoret.
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.
HERAX is looking for Consultants and Project Managers with experience from the pharmaceutical industry either from implementation of IT solutions or from working within the Life Sciences business area, or Life Science /IT graduates with preferably 1 – 2 years of experience.
As a Consultant/Project Manager, you will be part of or leading a small team of specialists, working closely with the clients in planning and executing process optimization- and IT projects within Research and Development. You will be involved in all project phases from the idea phase, to identifying the value adding areas, analyzing current and future processes and technology.
Radiometer Medical ApS, Brønshøj
If you are ready to set the direction for our Global Medical Affairs strategy for our many interesting and market-leading products and lead your own team of 4 Medical Advisors, then this could be your next career move.
- Lead and execute the Medical Affairs Strategy and operational plan to create value for key customers and the overall business
- Lead and develop the Medical Affairs team successfully included but not limited to performance management, talent management and training
- Accountable for understanding the external agenda
FMC Corporation, Hørsholm
We are looking for a talented individual for our European Innovation Center in Hørsholm to assume the responsibilities as a Country Registration Specialist. In cooperation with Nordic, European and Global colleagues you will be a key contributor then growing innovation is a key mantra within the company.
In your role as Country Registration Specialist you will prepare, maintain and submit registrations for FMS’s protection products in the Northern Zone. The job includes multiple interactions with various types of stakeholders, as national authorities and institutes, local farmers’ organizations, customers, development colleagues and business teams. The tasks vary substantially from day to day, and multiple projects are running in parallel.
Unomedical A/S, Osted
For our business unit ConvaTec B2B “Unomedical” at Osted, near Roskilde, we are looking for a committed Category Manager with the responsibility for Injection Molding and Resin Sourcing activities.
The successful candidate will be part of the Direct Sourcing Team of currently 7 competent employees working in close cooperation with other departments in the company especially Logistics, R & D, Sales & Marketing, QA/RA, and with our production sites in Denmark and Mexico. Yearly travel activity of approximately 40 days are to be expected.
- Drive price and contract negotiations with a strong focus on supplier relationship and cost optimization
- Identify potential suppliers for new and existing products and follow up on existing suppliers
- Participate in projects on new and existing materials ensuring a smooth running of current production at our suppliers
Danske Bank, Copenhagen
Do you have profound experience with AML concerning corporate customers? And do you have what it takes to drive change in a diverse and international environment?
We are looking for an AML specialist who is not only on top of the legal requirements, but can also help people understand and comply with them.
You will be working closely with the Head of Risk who is also in Copenhagen. The team is responsible for operational risk and regulatory risk, so your area of responsibility will be broader than just AML.
Your main responsibilities will be to:
- Develop and maintain AML procedures
- Train and communicate AML requirements to business, functions etc.
- Evaluate specific AML cases and advise on whether to on-board or exit and how to mitigate risks
FMC Corporation, Hørsholm
Based in our new established European Innovation Center in Hørsholm, you will be responsible for managing the sourcing of FMC’s requirements for the Commodity Chemicals and Functional Additives portfolios for all sites in the EMEA region.
Together with the Global Category Managers you will develop and implement strategies, manage key supplier relationships, coordinate the issuance of forecasts and volume allocation, and other internal communications regarding materials in the pertinent categories.
- Understand FMC’s businesses and work closely with the main stakeholders to align sourcing requirements to business strategies.
- Indentify and implement savings and working capital opportunities via synergies between plants and businesses, particularly within the European sites.
Palsgaard A/S, Juelsminde
Brænder du for, og har du viden omkring lovgivning og produktdokumentation for fødevarer eller emballage, så er du måske vores nye 'Heart Working' kollega.
Til Palsgaards Regulatory Affairs afdeling søger vi en løsningsorienteret og ansvarsbevidst kollega, der kan indgå i afdelingens daglige arbejde med produktinformation og dokumentation på en dynamisk og effektiv måde.
Dine arbejdsopgaver vil primært være at:
- besvare spørgeskemaer og spørgsmål fra kunder vedrørende produktdokumentation
- håndtere verifikationsanalyser, herunder planlægning af prøver og rapportering af analyseresultater
- registrering og oprettelse af produkter
Cobham SATCOM, Lyngby
Cobham SATCOM is looking for an experienced Export Compliance & Commercial Officer. The successful candidate will be primarily responsible for running and supporting all aspects of export compliance across the Cobham SATCOM sites and for driving the agent/intermediary process.
There is also potential to develop and support other contracts and commercial activities.
As an Export Compliance & Commercial Officer your main responsibilities will involve:
- Ensuring compliance with the overall Cobham corporate export requirements and support all escalations and approvals processes
- Proactively set out export compliance strategies and execution plans driving export compliance into all the legal entities within Cobham SATCOM
Compass Human Resources Group A/S recruiting on behalf of Sanofi in Hørsholm
As Medical Advisor for Sanofi, you will provide medical and scientific expertise and service for the diabetes and cardiovascular (DCV) team in Denmark. You will report directly to the DCV Medical Head Denmark and be a part of the Nordic & Baltic Medical Affairs organisation.
Sanofi has interesting products in the pipeline within both disease areas and you will be a crucial part in preparing the launches. This means that you will have an extrovert position having peer to peer discussions with key opinion leaders, discussing, developing and setting up relevant studies and data generation and projects as well as providing medical education internally in Sanofi and externally.
There could be several entries to this job, and your background could be one of the following: As a Medical Advisor, or another related experience as a Medical Doctor.
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.