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Legal Counsel Nordics
Moment recruiting on behalf of FOX Network Group in Copenhagen
FOX Network Group is seeking a flexible lawyer on a full-time basis to fulfill the position of Legal Counsel Nordics based in Copenhagen
As a lawyer for Legal Counsel Nordics you will be reporting to the Deputy General Counsel EU & Africa (based in Amsterdam). You will be a member of the Legal & Business Affairs-team responsible for Benelux, Nordics, Balkans, CEE and Russia, consisting of 12 lawyers. This team is part of an international legal department within 21st Century FOX with lawyers based all over the world.
- Act as adviser for all legal and business affairs matters within FNG Nordics, by providing legal counsel, legal risk assessment and guidance in the ordinary course of business and on special projects
- Be responsible for all corporate governance and regulatory matters, including media regulations
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Group Finance in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges across the global finance community. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
As a graduate with Group Finance you will be exposed to all areas of the team, working with both the team leads and team colleagues, including time spent with colleagues in Tax & Treasury.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within drug development - and are you passionate about the voice of patients and their caregivers?
Lundbeck’s focus is first and foremost on the patients suffering from Alzheimer’s Disease, Parkinson’s Disease, depression and schizophrenia, for whom we develop innovative medical treatments. In the Medical & Regulatory Science business unit, we strive to integrate patient perspectives in our activities.
Your job will be at the center of this, helping us to develop and operationalize patient and caregiver insights linked to the regulatory and medical aspects of our drug development strategies. We would therefore expect you to have a passion for patient focused drug development combined with the skills and educational background to understand and navigate medical and scientific data.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Corporate Communication in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges across the company. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
As Video Journalist, you play a pivotal role in Lundbeck’s proactive communication to employees and external stakeholders, i.e. the press. Working across the organisation you identify, research, shape and tell stories about Lundbeck’s progress and the difference it makes to patients and society.
LEO Pharma, Ballerup
Do you have several years of regulatory experience across the non-clinical and clinical areas, as well as project management of global regulatory submissions?
As Senior Regulatory Project Manager in our Regulatory Affairs Focus Team you will chair cross-departmental RA focus team(s) with members from RA CMC, Labelling, Submission Management and colleagues from our global affiliates. With you as the main driver, the team will prepare, drive and implement regulatory strategies.
Your key responsibilities will be to:
- Lead the regulatory focus team(s) for one of LEO Pharma’s strategic established products
- Prepare Global Regulatory Strategies and ensuring implementation hereof
- Ensure business perspective across functions and high regulatory quality
Radiometer Medical ApS, Brønshøj
Do you want to take commercial lead for our innovative sampler product portfolio and contribute to Radiometer’s Global Market Leader position in Critical Care Diagnostics?
In this job, you truly pull the strings when it comes to managing the product. You will be the global go-to-person for the sampler area with great global visibility in our organization working closely with the Global Marketing Team, Sales, Finance, Clinical & Medical Affairs, R&D, Supply Chain, RA/QA and our marketing and sales colleagues in our subsidiaries.
We offer an exciting position in a dynamic global business environment, with a unique opportunity to demonstrate results at all levels in the Radiometer organization and thereby further grow your career in Radiometer.
JKS recruiting on behalf of AltaPay in Søborg
AltaPay is growing fast and we are therefore looking for a high-performing Sales Executive to join our team based in Soeborg, Copenhagen.
We are looking for an ambitious and self-driven Sales Executive, who is interested in working for an exciting fast-growing Payments Business with solution selling to enterprise/large accounts. You will be responsible for the development and execution of the sales strategy, against a deliverable revenue target.
This is a full life cycle enterprise sales opportunity selling a retail omnichannel solution (eCommerce, Payment terminals and Acquiring) to a diverse range of businesses, across the Nordic market.
You will be responsible for building up the Nordic Market, developing the go-to-market strategy in identified retail vertical primary.
Coloplast A/S, Humlebæk
Are you data driven and looking for a role where you can impact the execution of our clinical studies?
Your job as a Data Manager (DM), is to prepare databases and administer study data for final analysis. You will get the opportunity to follow the investigations from the very start of the planning phase to the end of the study and thereby be involved in different phases of the investigations. With more detail, the tasks are:
- Prepare case report forms (questionnaires), data management plans as well as study validation plans and reports.
- Set up the database and data entry screens, planning, coordinating and managing data entry activities.
- Validate clinical data (set-up and testing of edit checks, query handling and quality control of the data).
3Shape A/S, Copenhagen
Do you have a passion for products and a great user experience? Do you want to make a difference for people needing dental treatment around the world? 3Shape seeks a Product Manager responsible for our Dental Design software, who has a flair for technology and the ability to translate customer and market needs into successful products.
Your objective will be to drive the development of our new Dental CAD software to ensure we maintain a leading position in the market. As member of the Dental Lab product management team, you will work autonomously and interact with stakeholders across all areas of the company, i.e. Development, Marketing, Sales, Regulatory Affairs and Customer Care. Besides, you will:
- Use state of the art technology, such as deep learning or augmented reality to realize superior product features
- Take part in continuing the development, testing, and implementation of new features and functionalities
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
Work in the CMC Regulatory Affairs area within an exciting and fast growing biotech company
Genmab has a robust pipeline of innovative human antibody therapeutics and a number of strategic partnerships are already in place with international blue chip companies.
As CMC Regulatory Affairs Manager, you will be responsible for operational and strategic regulatory input with an emphasis on CMC matters to support worldwide development and commercialization of the Genmab pipeline. You will be part of the operational teams directing and coordinating international regulatory submissions supporting the conduct of clinical trials. Furthermore, you will be supporting marketing authorization submissions to EMA and other regulatory health authorities.
Cook Medical, Bjæverskov
Engineer with a dedication to quality and creative problem solving.
Cook Medical is continuously developing to meet external as well as internal challenges. To ensure that we keep maintaining and improving our product quality and safety as well as regulatory compliance, we are looking for a new member of our CAPA Team.
You will be part of a dedicated team of 10 who is responsible for leading the CAPA’s in collaboration with the Product Sustainment, Production Engineering, Operations, Quality Engineering and Regulatory Affairs departments.
You will be facilitating the problem-solving process from the problem investigation and the root cause analysis and lead the implementation of the corrective and preventive actions.
LEO Pharma, Ballerup
Do you want to ensure that patients get affordable access to treatments that improve their quality of life? Can you translate global initiatives and requirements into good processes for collaborations with our local markets?
We have set ambitious goals for the region towards 2025. In order to achieve these, it is vital that we not only ensure that our business is profitable, but also that we create access to our treatments, as many of our patients are in an out-of-pocket situation. You will play a key role in achieving optimal market access in our markets by leading pricing activities and developing strategies that maximize value for LEO Pharma.
Your primary tasks will be to:
- Establish and optimize regional pricing strategies in close collaboration with the Global Pricing team and other relevant stakeholders.
- Ensure visibility of prices and pricing strategies and
Unomedical A/S, Osted
Vi søger en Regulatory Affairs Assistant til vores virksomhed ConvaTec, Infusion Care i Osted. Du vil skulle assistere vores regulatoriske team, der består af 4 Regulatory Affairs Specialister i forbindelse med registreringer og salg af vores produkter.
Som Regulatory Affairs Assistant vil du indgå i et af de 3 teams, der er samlet i kvalitetsorganisationen med omkring 50 medarbejdere. Vores dagligdag er præget af et godt samarbejde med en uformel tone og frihed under ansvar. Der er stor medindflydelse på planlægning og udførelse af eget arbejde.
- Vedligeholdelse af teknisk dokumentation i form af tekniske filer
- Vedligeholdelse og opdatering af relevante SOP´er i vores QMS
- Vedligeholdelse og opdatering af relevante regulatoriske databaser
Vi søger en selvstændig, talentfuld og faglig stærk Public Affairs profil, der med gennemslagskraft kan varetage vores medlemmers interesser i EU – til gavn for deres kunder og samfundet i øvrigt.
Arbejdsdelingen mellem kontoret i Bruxelles og København er organiseret ved, at vores eksperter i København leverer fagligheden og materiale til Europapolitisk afdeling, der herefter har til opgave at få det konverteret til slagkraftig interessevaretagelse.
Din kerneopgave er, sammen med dine kolleger i afdelingen, at være ansvarlig for interessevaretagelsen i forhold til Finans Danmarks EU- og internationale-sager. Det sker gennem deltagelse i forskellige mødefora af formel karakter og mere uformel networking og vidensdeling herom med resten af organisationen, udarbejdelse af policypapirer, baggrundsnotater, handleplaner, koordinering af indsatser og bidrag til nyhedsbreve.
LEO Pharma, Ballerup
Do you want to break new land and help taking LEO into a new era?
Your overall focus will be to provide medical and scientific input to the development, interpretation and documentation of clinical trial data to the projects for which you will hold the medical responsibility. As such, you will influence the direction for the development projects, how we set up trials, how we interpret results etc.
Your specific job functions include to:
- Act as medical expert in clinical development teams – project teams, clinical teams and study teams
- Drive the medical and scientific content of Clinical Development Plans
- Contribute to clinical trial protocols, clinical trial reports, clinical regulatory documents, investigator’s brochures and publications
Ferring Pharmaceuticals A/S, Copenhagen
Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world.
We are looking for a new colleague to fill a permanent Pharmacovigilance Coordinator position as soon as possible. Are you interested in becoming part of a dynamic team? Do you thrive by working in an international environment? In addition, are you structured and have good planning skills? Then we may just have the right job for you.
You can expect to become an integrated member of a highly motivated and dedicated team collaborating with the therapeutic teams, business support and compliance, PV technology team in Global Pharmacovigilance, Clinical Development, Regulatory Affairs, Authorities, Affiliates and Partners.
Grundfos A/S, Bjerringbro
Do you want to be responsible for executing M&A transactions for one of the global leaders within water solutions?
We have an open position as M&A Specialist in Corporate Affairs, M&A Department, where you will be project managing M&A transactions and play an active role in the origination, execution, negotiation and implementation of transactions.
Your key tasks will be to:
- Project management of M&A transactions, including driving due diligence processes and negotiating deals
- Design and structure M&A processes
- Capable of (co-) developing new opportunities
- Building and maintaining good working relationships with investment bankers and targets
- Ensure strong alignment with internal stakeholders and the ability to challenge assumptions and prejudices
Ambu A/S, Ballerup
Do you see yourself lead the Clinical Research & Biosafety Department in a global company that works to save lives and improve patient care?
As Director for the Clinical Research and Biosafety Department, you will manage a team of eight professionals in Denmark and function as the professional responsible for the clinical team in the USA and in Asia. You will work as a hands-on manager with your own deliverables, in close collaboration with Global Innovation and Marketing to develop and introduce medical devices within the fields of visualisation, anaesthesia and patient monitoring & diagnostics.
Your overall responsibility is to lead the Corporate Clinical Research & Biosafety team, and to ensure that Ambu's product portfolio is supported by the necessary clinical and biosafety documentation and that this documentation is updated correspondingly.
Are you eager to work in a dynamic company where new challenges and opportunities are part of your every day life?
PharmaLex is the leading service provider for the worldwide pharmaceutical industry in regulatory affairs, pharmacovigilance and development consulting. We are specialized in effectively designing all aspects of drug and medicinal product registrations – ranging from early development and market entry to product maintenance activities.
As a part of our Regulatory Affairs team, your duties will primarily include planning, preparation and submission of regulatory documents. The main responsibilities of the Regulatory Affairs Manager will include:
- Compilation of new authorization applications
- Product launch in the Nordics
- Product maintenance e.g. variations including CMC support
- Publishing activities with eCTD manager
Coloplast A/S, Humlebæk
As our new Vigilance Officer you will be part of the global Vigilance process operating in a dynamic and professionally challenging working environment. Your main responsibilities will be to diligently investigate adverse events and report to national competent authorities according to applicable regulatory guidelines and timelines. Furthermore, you take the lead in handling safety issues related to the use of our products and deliver Vigilance data for registration of products in new markets.
As an extra rousing challenge the new Medical Device Regulation is coming up and we would expect you to be engaged in implementing it. You will be able to contribute significantly to the ongoing improvement of the global vigilance process in Coloplast.