31 job matcher din søgning
SOS International a/s, Frederiksberg
Vil du være en del af en spændende, international arbejdsplads, hvor du har mulighed for at hjælpe og gøre en forskel for skandinaviske patienter over hele verden?
SOS International assisterer skandinaviske rejsende overalt i verden på vegne af forsikringsselskaber. Det sker via vores døgnåbne alarmcentral 24 timer i døgnet – 365 dage om året.
Vi søger en kollega til Transport Centeret med specialefunktion som SAS Medical Assistance. Stillingens primære formål er at godkende og planlægge medicinske transporter for SAS samt andre flyselskaber, som SAS har kontrakt med. Dette gøres ved medicinsk at vurdere de sager, som kunderne/forsikringsselskaberne sender til SAS og derefter bestille/arrangere transporten med det nødvendige udstyr og assistance.
3Shape A/S, Copenhagen
Are you ready to pursue your scientific career within digital health working with 3D scanners as well as software medical devices in a global setting? Then 3Shape offers a unique opportunity to work as a Scientific Manager in the center of Copenhagen at Kongens Nytorv.
The main purpose of the job is to develop and maintain our clinical evidence documentation as well as to facilitate post market activities in order to support our products with regards to safety and clinical performance as well as claims. You will be cooperating with multiple stakeholders internally as well as externally.
Job responsibilities include:
- Preparation and maintenance of Clinical Evaluation Reports (CERs)
- Ensure that the clinical evidence requirements and the CERs for our products comply with current and future global medical device guidance and regulations
3Shape A/S, Copenhagen
Are you ready to continue your regulatory career within digital health working with 3D scanners as well as software medical devices in a global setting? Then 3Shape offers a unique opportunity to work as our new Regulatory Affairs Specialist in the center of Copenhagen at Kongens Nytorv. This opportunity will help you develop within future disruptive health technologies together with the entire organization and with exposure to senior management.
As a Regulatory Affairs Specialist, you will join our Global Regulatory Affairs team based in Copenhagen. We are currently a team of nine Regulatory Affairs Specialists/Coordinators and one Scientific Manager with diverse backgrounds. Six additional colleagues are expected to join the team in 2018. You will interact with a wide range of stakeholders and especially with R&D, Product Management, Global Sales offices, and external consultants worldwide.
Sandoz A/S, Copenhagen
Do you want to work for a Global Pharmaceutical company where you will get recognized for your hard work and commitment? Look no further, apply today for Commercial Manager OTC. The Nordic OTC business is an important contributor of Sandoz future growth strategy, and is expected to grow significantly in the years to come.
The purpose of the Commercial Manager role is to lead the commercial sales activities towards pharmacy chain customers in Denmark, Sweden and Norway. In addition the Commercial Manager will also be sales manager for a field based sales force visiting pharmacies in Denmark. The Commercial Manager reports to Franchise Head OTC Nordics, and is end-to-end responsible for all commercial activities regarding the OTC portfolio in Denmark, Sweden and Norway.
Ferring Pharmaceuticals A/S, Copenhagen
As Clinical Project Leader (CPL) you are part of the Global Clinical Operations team, currently consisting of approx. 50 experienced and highly dedicated persons (CPLs, Trial Managers, Document Managers and a Clinical Project Coordinator).
The CPL is representing Global Clinical Operations as core member of the Global Project teams. The CPL is responsible for delivering tactical and strategic input to the development plans and ensure the most appropriate clinical program is planned and conducted. The CPL works closely with the global project teams, therapeutic area functions, medical writing and trial management teams to deliver excellent clinical results to plan. The successful CPL will be the trusted clinical expert, be efficient in stakeholder management, develop and ensure project standards, and be confident in working with empowered trial teams.
Jakob & Partners ApS, Copenhagen
Pharmaceutical sciences, biotechnology, medical devices
If you want to work for a highly successful company providing research and analyses of markets within the pharmaceutical and biotechnological industries, you should consider this position in Jakob & Partners. You will be part of a highly qualified team with expertise within life and pharmaceutical sciences, market insights and economics.
Your job will be exciting and challenging and will demand a high degree of flexibility. You will become part of a highly qualified, truly international and top performing team. You will be working on a range of projects within different therapeutic areas and develop a unique insight of the pharmaceutical and biotechnological markets through training courses and interactions with internal and external experts.
Interacoustics A/S, Middelfart
Would you like to use your skills and knowledge of regulatory affairs processes in an international set-up together with other highly qualified regulatory affairs specialists? Then we have a great opportunity for you.
In your new role, you will be in close contact with the Sales, R&D and Product Management functions in the companies in the Diagnostic Division. The division consists of several individual brands, including Interacoustics, placed in Denmark, UK, USA and Germany. Your role allows a close collaboration with these brand’s local representatives in the markets where we register and sell our products. You will be the facilitating point of contact between each brand and the local representative.
Arla Foods, Viby J.
Do you have a dare-devil and entrepreneurial mind-set? Are you passionate about making a difference and working towards a higher purpose? Then Arla’s Summer Internship Programme is the perfect way for you to spend the summer of 2018!
During the internship, you will be based at Arla’s global HQ in Aarhus, Denmark. Three days a week you will have assigned tasks and work in a specific department with a sponsor and during the remaining two days, you will get the opportunity to work on an innovation project with your fellow interns.
Throughout the internship, you will be offered to participate in e.g. personal development sessions as well as dairy- and farm visits with the purpose of getting the best possible understanding of the process from cow to consumer.
Hays Specialist Recruitment A/S recruiting on behalf of UCB in Copenhagen
Unique opportunity to secure, maintain and enhance UCB's Patient Solutions in Denmark.
On behalf of our client, UCB, Hays is looking for a talented Country Market Access Lead to provide the best solutions to patients across Denmark. The main responsibility of the role is to secure, maintain and enhance the UCB’s Patient Solutions by gathering and integrating local payer as well as ecosystem insights and translating these into value-based access solutions for the UCB developmental and in-market portfolio.
With direct reference to the Market Access Director Northern Europe, you will be joining a truly professional local team and enjoy great collaboration with the Northern European Market Access team.
Academic Work recruiting on behalf of client in Herlev
Academic Work is on behalf of our client looking for a Purchase Manager for their office in Herlev. As Purchase Manager, you will work on a daily basis with procurement of pharmaceutical goods, with a focus on gaging the time, quantity and quality needed for best efficiency and optimized costs. You will be responsible for managing and executing projects from A to Z and will be responsible for all stages of the process, including initial market research, identification of and communication with suppliers and clients, price-negotiations, order creation etc.
- You have between 2-5 years’ experience within technical purchasing, preferably within foreign trade or the industrial sector. You may have previous titles such as Purchaser, Purchasing Assistant or the like.
- You are fluent in spoken and written English
- You are proficient in Word, Excel, Outlook
HKScan Denmark A/S, Vinderup
HKScan Denmark is searching for an experienced and independent Poultry veterinarian/-consultant to continue developing and strengthening our cooperation with our many skilled pro-ducers of poultry.
Your role is concerned with our most important raw material – the chicken (quality, health and welfare). While focusing on creating value for HKScan, you at the same time help our producers create value in their own production.
Primary areas of responsibility in the job:
- Daily cooperation with our producers on subjects like animal health, animal welfare, slaughter quality, productivity etc.
- Maintain and develop a value creating partnership with our producers
- Utilize, maintain and develop analytical tools / databases / systems to support both our producers and internal decision processes in HKScan. Can be within health surveillance, use of antibiotics, animal welfare, development of productivity, finances etc.
We are looking for two new colleagues to our Regulatory CMC department. We are a team of 9 people handling CMC documentation for ALK tablet portfolio. The team is part of Global Regulatory Affairs which counts approximately 50 people in Hørsholm.
We are looking for two team members that are dedicated to communication of complex scientific matters in a written form. We believe you have experience with global regulatory CMC requirements for biological products and Regulatory Life Cycle Management of medicinal products globally. We also hope you enjoy cross-functional interactions.
Field of responsibility
- Responsible for writing and maintaining regulatory CMC documentation for worldwide submissions
- Responsible for having an overview of submitted and approved CMC documentation in different regions
CO-RO A/S, Frederikssund
HQ position within food regulatory with global perspective.
As a part of the 5-member regulatory team, you will participate in supporting tasks and issues on our markets covering Europe, Middle East, Africa, Far East Asia and Caribbean.
The department supports marketing of existing products, new product development, new packaging development, labelling and marketing within food and marketing regulations globally.
Fields of responsibility:
- Support on matters related to appointed countries and topics
- Follow and maintain food regulatory knowledge on countries and topics
- Food regulatory support on innovation projects, including approval of raw materials products, labelling, artwork and marketing
ORIGIO a/s, Måløv
ORIGIO a/s, a world leader in culture media and laboratory equipment for assisted reproduction, has an opening for a skilled Project Manager in the Media Development department, R&D in a full time position at the headquarter in Måløv.
You will get the opportunity to work in a dynamic and energetic team within new product development in a med-tech company committed to “making the number one dream of infertile couples come true”.
As Project Manager in cross functional teams, you will manage and execute project plans within new product development of media for IVF. This includes being responsible for planning regular team meetings and resources to meet project goals, preparation of project charters, development of product documentation according to external and internal guidelines for Medical Device products and reporting of monthly project progresses to internal stakeholders.
Badenoch & Clark søger for Lely Nordic A/S i Fredericia
Lely Nordic søger en ny kollega til deres tekniske support-team. Den nye medarbejder skal bistå i teknisk support og træninger til teknikere, som udfører installation og service hos slutkunder. Teknikerne er ansat hos Lely Center, hvilket er dedikerede forhandlere af Lelys teknik til mælkeproduktion.
Hos Lely har alle medarbejdere en selvstændig stilling hvor der arbejdes med ”frihed under ansvar”. Det vil sige, at du i stort omfang selv kommer til at planlægge og udføre din arbejdsdag.
- Teknisk produkt-træning på ovenstående produkter (træningslokale, hos Lely Center eller hos slutkunde).
- Udarbejdelse af trænings- og informationsmaterialer.
- Deltage i 24/7 teknisk helpdesk.
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
A senior CMC position in a fast growing biotech company
As Senior CMC Professional at Ascendis Pharma, the main success criteria is to create a good understanding of deliverables to the project(s) as part of the CMC Project Team. Additionally, the Senior CMC Professional must establish a close and high-standard cooperation within the CMC Project Team and become a value-adding resource to them.
Your main responsibilites are:
- For the Phase 3 project TransCon hGH, the Senior CMC Professional will, in cooperation with the Drug Product responsible Director, be responsible for designing, executing, and reporting pharmaceutical development studies supporting the GMP Drug Product
- Ensure statistical tools are used where relevant
- Ensure that tasks are conducted optimally with respect to quality, timeliness, and budget
Sandoz A/S, Odense
Do you want to work for a Global Pharmaceutical company where you will get recognized for your hard work and commitment? Look no further; apply today for Key Account Manager OTC.
The purpose of the Key Account Manager role is to build, own and execute business plans to secure a solid professional relationship with pharmacies. The assigned territory is Funen and Southern part of Denmark, where the Key Account Manager is expected to meet sales goals, drive territory sales performance, market share and optimal resource utilization. The Key Account Manager will develop effective professional business relationships with customers that support delivery of business results for customers and Sandoz across the Danish OTC portfolio, and will differentiate Sandoz as a leader in selected specific therapeutic areas.
Novo Nordisk A/S, Bagsværd
Are you interested in clinical trials, operational project management and pharmacovigilance? Do you want to cooperate with stakeholders across the organisation? Then we may have the right job for you. We are looking for an Event Adjudication Adviser to join our Safety Operations (SO) Event Adjudication department. The position is a 1 year maternity cover.
As an Event Adjudication Adviser you will be a driving factor between Safety Operations, Data Management, Global Development and external service providers (CROs) dealing with event adjudication in selected clinical development projects. You will make the first assessment of the events and ensure that all documentation is made timely available for the final event adjudication.
Er du en stærk motivator og klar til at udøve Arlas ledelsesmæssige værdier og har du lyst til at stå i spidsen for et dygtigt team af operatører på Europas største Child Nutrition spraytørringsanlæg spray 6 - så har vi måske rollen til dig på ARINCO i Videbæk.
Som leder for 10 dygtige operatører på Arinco Spray 6 er dit primære ansvar personaleledelse, herunder opretholdelse af et sikkert, sundt og godt arbejdsmiljø. Du er garant for et stabilt højt kvalitetsniveau i produkter fra spray 6 og herigennem sikring af kvalitetsprodukter til de sensitive forbrugere af vore produkter.
Du arbejder på fast daghold men bærer ansvaret for afdelingens resultat 24-7. Vores kultur er LEAN, hvorfor målstyring og brug af de forskellige LEAN-værktøjer i dagligdagen er en selvfølge.
LEO Pharma, Ballerup
A key operational challenge for LEO Pharma will be to ensure GXP and Regulatory compliance in an expanding and increasingly complex network of external manufacturing partners. We need you to join our External Manufacturing Quality team in a newly established position.
It is our defined goal to succeed in providing continuous quality oversight of LEOs CMOs. In this connection you will have responsibilities within (but not limited to):
- Establishment of solid, robust and transparent Quality Agreements as framework for the quality related partnership with the CMOs
- Close Quality relations with CMOs including regularly meetings
- Periodic quality reviews such as audits and PQR’s