29 job matcher din søgning
Vi søger en ny kollega til en ledig laborantstilling i in vitro-sektionen i vores afdeling, Exploratory Toxicology, som vil være med i vores arbejde med at identificere og udrede toksicitet af potentielle nye lægemiddelkandidater i Discovery projekter på Lundbeck.
Vi søger en laborant eller en person med lignende baggrund. En stor del af arbejdet vil være screening af stoffer for toksicitet ved hjælp af multiplex assays med high content analyseudstyr og med enzymatiske assays. Det vil være dit ansvar at stå for disse assays, analysere og rapportere data efter en oplæringsperiode.
Vi arbejder kontinuerligt med at forbedre de eksisterende assays og udvikle nye og derfor vil jobbet også involvere metodeudvikling, typisk i samarbejde med en af afdelingens akademikere og de øvrige laboranter.
Indrykket 27. april
Do the words DATA INTEGRITY, GAMP 5, RISK MANAGEMENT and COMPUTER VALIDATION ring a bell? Do you have experience working with these topics in the pharmaceutical industry? Are you flexible and open minded and looking for new challenges and opportunities?
If yes, we are looking for a colleague, with a strong background in IT quality, for a new position in our team. You will join the 3 colleagues in the Corporate Quality Assurance IT department.
In close cooperation with the team, the successful candidate will be tasked with solving a broad suite of tasks that range across the responsibilities of the department.
You will work with a variety of stakeholders, system owners and business areas within Lundbeck in order to help ensure the quality and compliance of IT systems in the entire company.
Indrykket 27. april
Vi søger en laborant eller laboratorietekniker til ledig stilling i Department of Bioanalysis. Afdelingen har ansvar for at udvikle og validere bioanalysemetoder til kvantitativ bestemmelse af lægemidler og metabolitter i biologiske prøver, samt at analysere prøver fra såvel non-kliniske som kliniske studier. Vi er i dag 15 medarbejdere i afdelingen, hvor laboranter og akademikere arbejder tæt sammen i en travl, men inspirerende hverdag. Vi kan tilbyde nye og moderne laboratorier - og kontorfaciliteter, og du vil opleve en positiv atmosfære og godt kollegialt samarbejde i afdelingen.
Din primære opgave bliver at analysere biologiske prøver fra non-kliniske og kliniske studier. Metodeudvikling og metodevalidering omfatter udover det praktiske arbejde skrivning af protokoller, udarbejdelse af metode SOP’er samt rapportering af valideringsdata. Arbejdet udføres i henhold til GLP/GCP og efter FDA og EMA guidance.
Indrykket 27. april
Er du interesseret i lægemiddelfremstilling eller pakning, og har du lyst til at starte din karriere hos Lundbeck, så har vi en spændende uddannelse som Industrioperatør klar til dig.
Vi søger 3 motiverede og fleksible lærlinge, som arbejder samvittighedsfuldt og altid kvalitetsbevidst. Vores 3 nye lærlinge er til afdelingerne Liquid & Sterile Production (steril produktion), Solid Bulk Production (tablet produktion) og Finished Goods Production (produktion af pakninger).
I din lærlingetid vil du – i tæt samarbejde med erfarne kollegaer – få erfaring med:
- Discipliner inden for fremstilling af lægemidler/pakning
- Produktion i henhold til GMP (Good Manufacturing Practice) og arbejdsmiljøregler.
- Udfyldelse af produktionsdokumentation
- Rengøring af udstyr
- Daglige administrative og praktiske opgaver
Indrykket 27. april
At Oticon, we are at the forefront of the latest technology, constantly working to improve hearing solutions for our users in order to strengthen and develop our business. Do you want to be a part of our continuing success please apply for the vacant position Product Reliability Engineer.
As Product Reliability Engineer you will be working closely together with Product Quality Managers to give support to R&D projects by reviewing designs, making test plans and testing specific constructions.
In addition to this, this position will also include validation and qualification activities for our test equipment and test methods.
Indrykket 25. april
Do you want to work with the most advanced technologies alongside colleagues, who are best in class? How does working in agile teams with a large degree of knowledge sharing sound to you? Finally, do you want to work with us in making the lives of millions of people worldwide better?
In your role at Quality Requirement Manager, you will be driving and facilitating a number of working groups with participation from Quality and R&D.
You will be the expert in the requirement framework and way of working with requirements and will be supporting your colleagues in this. Your expertise will cover the use of the requirement tool IBM Rational DOORS as well as the compliance with processes.
Your main tasks will be:
- Facilitating of Quality Requirement development in cross-functional working groups
- Conducting formal Quality Requirement reviews with stakeholders
Indrykket 24. april
We are looking for a Research Scientist having experience with technologies such as immunohistochemistry, in situ hybridization and autoradiography.
By contributing with your highly qualified knowledge around histology/anatomy you will be part of a team effort aiming at translating basic science into applied research. The ultimate goal of your effort is to validate and progress CNS target opportunities from an in vitro perspective. Your daily job will primarily consist of lab work and technician supervision to support our pre-clinical research projects with information about quantification and distribution of targets. This also implies how targets are affected by pharmacological interventions or animal models of disease phenotypes.
You will also be involved in identification and assessment of new targets based upon your knowledge around immunohistochemistry and protein-protein interactions.
Indrykket 21. april
Do you have strong experience with information management and are you a structured person with a keen eye for details? Then we have the right job for you at Oticon. We are experiencing a substantial growth in our business and want to attract an ambitious and engaged Product Information Specialist to our digital marketing team.
You will be responsible for our newly introduced Product Information Management (PIM) system, ensuring that our product data is accurate and continually refined in response to established business goals and objectives through proper documentation, system design, while providing excellent customer service to internal and external customers. You will have a close cooperation with both Masterdata and IT, but you will also will work with many different people throughout the whole company.
Indrykket 20. april
As Safety Scientist, you will be part of a team responsible for reviewing Adverse Reaction reports received from Health Care Professionals, patients, regulators and other sources from around the world. You will take part in monitoring the safety of our compounds on the market and you will help prepare key pharmacovigilance reports such as Periodic Safety Update Reports, Signal reports and responses to requests from regulators. You will join one of our safety teams and will get an opportunity to be part of the collaborative atmosphere, working together with our senior medical staff to monitor and secure patient safety.
We offer an interesting job in an ever more demanding area of the pharmaceutical industry in a global environment, with an individually tailored training package, flexible working conditions and good career opportunities.
Indrykket 18. april
Together with 40 very skillful and enthusiastic colleagues, you will join us in challenging conventional electro acoustic and mechanical solutions to improve end-user and customer satisfaction.
In your new job you will be part of Oticon’s Hardware Function, more specific the Hearing Instrument Design (HID) group. The excitement this group faces on a daily basis is the development of highly challenging platforms, due to the high degree of functionality that hearing instruments offer. Furthermore, we focus on developing our platforms to fit multiple brands adding to the complexity. The team works closely together with other competences i.e. audiologists and engineers specialized in amplifiers and embedded systems.
Your responsibilities include:
- Acoustic system design and development
- Platform calibration/settings
- Design specifications
Indrykket 18. april
We are hiring a communication specialist to drive our news flow and tell the exciting stories about Lundbeck
Lundbeck wants to engage in an active and open dialogue with external media and other stakeholders. We are looking for a new colleague to assume the position of Communication Specialist and play a key role in driving our news flow and proactively communicate stories about Lundbeck in external and internal media.
The corner stone of this position is to drive and coordinate Lundbeck’s news flow to ensure that we proactively communicate fascinating and exciting stories about the company and its performance to enhance the visibility of and trust in Lundbeck. The job requires the journalistic sense for and ability to carve out stories of interest to different stakeholders, including external media.
In this role you will take part in the ongoing servicing of external media, including handling of media inquiries.
Indrykket 11. april
In the role as Chief Product Owner for audiology and embedded software solutions, you will become a pivotal part of the R&D unit “Audiology and Embedded Systems” (AES).
As the Chief Product Owner you will be responsible for setting direction and priorities for the audio features in the hearing solution products within the WDH.
Your main responsibilities will be:
- Prioritizing of AES deliveries across the entire product suite and the entire portfolio and convey this to relevant stakeholders.
- Drive portfolio management for audiology, digital signal processing and embedded software in R&D and make the priorities transparent to the organization.
- Close collaboration with new business introduction, market category management as well as RD management on the priorities over time, releases, programmes and features.
Indrykket 10. april
Do you have experience in setting up anechoic chambers and test advanced audio products against product requirements and regulatory requirements? Do you thrive by working with products being a combination of hardware and software? Do you believe that testing is a proactive and solution orientated discipline? Then you might be our new system verification engineer.
Your main responsibility in this role is to verify our hearing solutions prior to being handed over to mass production. To this end your main tasks consists of the following:
- Preparing and executing tests in anechoic chambers
- Measuring and reporting acoustical output
- Test hearing instrument audio properties under different environments and circumstances
- Debugging and critically assessing test output in order to provide constructive feedback to developers
Indrykket 10. april
You will have 3 main responsibilities: projects, optimization of processes & equipment and second line support. The main project activities for the coming years are the implementation and qualification of 2 new blister lines and implementation of Serialisation and Traceability according to global regulatory standards.
As a project engineer you will be part of the project team responsible for the entire project lifecycle including activities such as user requirement specification, vendor selection, installation, qualification/validation until handover to the end user.
The projects vary in scope and complexity, but often involve a high number of participants from different parts of the organization, requiring coordination and follow up on activities to meet deadlines.
Indrykket 7. april
As Bioinformatics Expert, you apply your expertise within bioinformatics and statistical modelling to address biological questions. Based on your theoretical knowledge and your exploration of complex data, you generate actionable biological insight together with the team.
You and the team will work closely together with biologists and clinicians to improve the biological understanding of the targets and diseases, and to investigate and define patient segments based on a variety of data types including genomics and clinical data from the CNS indications on which Lundbeck focuses; Schizophrenia, Depression, Alzheimer’s and Parkinson’s Disease.
You participate in preparing scientific publications, and will work with collaborators within academia, scientific communities and international consortia.
Indrykket 7. april
Do you have a background from SW development and solid experience from Product Quality in a large international company? Then come join us for an exciting career opportunity at Oticon – a company truly known for its commitment making the world’s finest hearing solutions.
In your new role, it is your responsibility to make sure that our SW-products fulfil the user’s expectations as well as the regulatory requirements. You can look forward to a wide portfolio of interesting and challenging tasks, and your main focus will be to:
- Plan and execute activities related to quality assurance of SW products being developed
- Collect and give feedback in relation to project market issues related to SWQ
- Establish and maintain a SW quality plan for R&D projects
- Establish and maintain SW Requirements Verification Traceability matrix for R&D projects
Indrykket 7. april
Has your career given you deep experience within the very lowest levels of embedded SW? Are you ready to take your career to the next level by applying that experience to one of the most advanced technologies within audio and communications systems? Then apply to join our highly skilled engineers in their daily battle with severe restrictions on power consumption, memory and cycles in one of the most innovative health technology companies.
Your main tasks will include:
- Design, implementation, verification and documentation of embedded software
- Involvement in IC specification and pre-tapeout verification
- Wakeup and validation of IC prototypes
- Support of Hearing aid hardware development
Indrykket 5. april
Are you looking to take the next step and kick-start your career combining business understanding with Information Technology?
As our new Graduate, it will be your responsibility to lead assignments and projects with the aim of bridging the business and information technology. You will engage with a broad set of stakeholders varying from Corporate IT Management to different stakeholders in our business areas, as well as vendors and subcontractors.
You will rotate between 3-4 selected areas in IT:
- IT Management (CIO’s office)
- Security & Projects
- Application Solutions
Indrykket 4. april
Are you looking to take the next step and kick-start your career within supply chain management?
In this graduate track, you will be anchored in External Supply Chain where you will have the operational and tactical responsibility for a group of suppliers. It will be your task to ensure availability of products, by developing forecasts, ordering and monitoring inventory development. You will learn to apply Lean tools and drive the performance of your suppliers via Lundbeck’s Supplier Performance Management System.
After ramp up you will be tasked with developing a more robust process across the operational, strategic and financial aspects of sourcing. This includes rotation and collaboration with areas such as Group Sourcing in Valby, Denmark and Finance in Krakow, Poland.
Indrykket 4. april
Are you looking to take the next step and kick-start your career within Regulatory Affairs then we have the Graduate Programme just for you.
Your home area will be the Regulatory Dossier Management Department (RDM) that focuses on executing the regulatory strategies for Lundbeck’s development projects and marketed products. RDM is involved in all regulatory activities across the RA value chain and plays an instrumental role in ensuring a successful registration processes for clinical trials and marketing approvals across the world.
You will be involved in and manage all types of submissions to Competent Authorities worldwide:
- Initial marketing authorization applications
- Variations to and renewals of marketing authorizations
- Periodic Safety Update Reports
Indrykket 3. april