28 job matcher din søgning
LEO Pharma, Ballerup
Are you passionate about improving lives of millions of people by developing treatments for skin diseases?
This is your chance to join one of the world’s leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world.
You will have a key role on primary packaging development and maintenance and you will be in collaboration with development and manufacturing partners. It will be your responsibility to establish, review and maintain documentation for regulatory approval of primary packaging.
Furthermore, the area of responsibilities will be:
- Development and maintenance of primary packaging in compliance with current regulatory and GMP requirements and standards securing quality, reliability and launch readiness.
- Executing technical tasks related to primary packaging development, e.g. materials selection and specification, testing & verification
Chr. Hansen A/S, Hørsholm
We are looking for a research technician (laborant) for our Strain Development Department, in the Bacterial Physiology unit, Discovery function of R&D at Chr. Hansen A/S in our headquarters in Hørsholm, Denmark.
As laboratory technician within the Bacteriophage area in the Strain Development department you will work on different tasks within phage biology and will also be directly involved in strain development activities.
The different tasks include:
- Phage identification with common methods and development of new methods for phage identification
- Phage purification and maintaining of the phage collection
- Phage typing of production strains
Ferring Pharmaceuticals A/S, Copenhagen
We are seeking a new colleague to a newly established Global Regulatory Affairs, Clinical and Non-Clinical department at Ferring. Would you like to join us in a challenging and interesting position as Senior Regulatory Affairs Manager within Global Regulatory Affairs?
The Clinical and Non-Clinical department within the Global Regulatory Affairs is responsible for the regulatory activities up to the initial approvals in ICH countries for all global projects requiring clinical development, and supports market expansions worldwide from the Clinical and Non-Clinical regulatory perspective.
The Senior Global Regulatory Affairs Manager plays a key role in ensuring regulatory approvals of IND/CTAs and NDA/MAAs, developing global regulatory strategies, and managing scientific advice meetings with Health Authorities.
AJ Vaccines A/S, København
Vi søger to dygtige procesteknologer, laboranter eller lignende til downstream-teamet i MPP Unit. MPP Unit fremstiller kighostekomponenten (aP) til vores vacciner. Du bliver en del af den spændende proces, da vi skal øge produktionen markant de kommende år.
Dine primære arbejdsopgaver bliver kromatografisk proteinoprensning samt inaktivering af det oprensede aP toxin.
- Oprensning af proteiner på Äktaproces-søjlesystemer
- Fældning og inaktivering i LAF-bænk
- Udarbejdelse af batchdokumentation
Vi tilbyder et spændende og varieret job i en virksomhed med høj faglighed, hvor du i høj grad selv er med til at præge din hverdag. Du vil få en stor kontaktflade med dygtige og engagerede kollegaer. Du vil få gode muligheder for udvikling på det faglige og personlige plan, samt et bredt kendskab til vacciner og biologiske lægemidler. Vi glæder os til at få dig som vores nye kollega.
Do you have profound experience with regulatory CMC for biopharmaceuticals? Would you like to share your experience and be part of building up expertise within biopharmaceuticals across Lundbeck?
Lundbeck has traditionally worked with small molecules, but we are now also aiming to develop the competences necessary to be a key player in development of biopharmaceuticals (such as monoclonal antibodies). You will have an important role in this new strategy.
In your new job you will be:
- Responsible for all Regulatory CMC activities on biopharmaceuticals development projects
- Responsible for developing the Regulatory CMC strategy for assigned projects
In the position you will have the opportunity to be a central part of developing a strong and highly competent biopharmaceuticals team in Regulatory Affairs, and shaping the biopharmaceuticals environment at Lundbeck together with colleagues within and outside RA.
AJ Vaccines A/S, København
Vi søger en akademiker med lægemiddel videnskabelig baggrund eller lignende, der brænder for at arbejde med GMP og Compliance.
Vi er 13 medarbejdere i GMP/Compliance-teamet, der er en del af supportfunktionen i Fill&Finish. Der er 6 andre teams i Fill&Finish, der tilsammen omfatter lidt over 100 medarbejdere. Du vil sammen med teamet udfylde en vigtig funktion, i at yde support til de andre teams i afdelingen, med fortsat at være i compliance.
- Udarbejdelse og vedligeholde af GMP-systemer og –dokumentation til at understøtte Fill&Finish
- Udarbejde, gennemgå og godkende relevant GMP-dokumentation
- Behandling af afvigelser og CAPA’er
Vi tilbyder spændende arbejdsopgaver i en international anerkendt virksomhed med høj faglighed og stort engagement. Du vil få en stor kontaktflade med dygtige kolleger i et miljø, hvor faglig sparring er en naturlig del af hverdagen.
LEO Pharma, Ballerup
Do you want to make a difference in a challenging position?
As a Submission Manager your overall objective is to plan, manage and facilitate the delivery of submissions within a given product/portfolio. This position is the overall accountable and responsible for project managing individual submissions under an asset, from planning through to case closure, under the guidance of a senior colleague. This position involves close collaboration with LEO Pharma’s global submission sourcing partner.
Your priority tasks will be:
- Monitoring progress performance via project plans in accordance with LEO Pharma’s planning process
- Authoring and reviewing Module 1 documentation
- Coordinating the review of published outputs
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
Great influence on a newly established department
As Manager Process Validation at Ascendis Pharma, the main criteria of success will be, in cooperation with CMC, to establish and ensure reliable and robust chemical manufacturing processes at CMOs that are ready for PPQ and eventually market supply for intermediates and drug substance in one of Ascendis Pharma’s development projects. In addition, you will be a value-adding resource, actively contributing within the CMC and PS project teams on challenges related to chemical processes and manufacture.
Your main responsibilities are:
- External manufacturing of peptide conjugates, including solid phase synthesis
- Pre-PPQ and PPQ activities
- Establishment of continuous process monitoring programs for commercial manufacturing
Hartmanns A/S recruiting on behalf of DTU
Do you have management and leadership skills as well as a passion for academic research? Do you want to take the lead of a division that works on creating sustainability, more efficient energy systems and climate-resilient societies? Then this is a unique job opportunity.
The System Analysis Division is part of Management Engineering – one of the biggest departments of the Technical University of Denmark. Systems Analysis is an internationally well-established division doing high level research within energy, transport, climate change, urban systems, and sustainable development.
The division develops and applies methods from systems modelling, economics, econometrics, statistics, spatio-temporal analysis, and value chain studies.
ROCKWOOL International A/S, Hedehusene
As project manager, you will be tasked with managing one of our new development projects in close collaboration with skilled specialists. At the current stage of the project, we do not hold all the answers. Therefore, you will play a central role in finding the right solutions and determining which way to go to move the project forward.
Bridging your knowledge of chemical engineering with strong project management skills, your key responsibilities will be to ensure that the project stays on track and that we deliver on our goals.
Doing so, you will collaborate closely with a broad range of stakeholders – from our lab to production sites across Europe. Therefore, you can expect to travel 40-60 days a year, e.g. when visiting factories to make on-site testing.
Senior Clinical Trial Manager
Zealand Pharma A/S, Glostrup
The department is part of Clinical Development and is composed of a dynamic team with enthusiastic and professional colleagues. We have an open and respectful environment encouraging knowledge sharing and where we welcome new ideas.
Due to the high number of new trials that we will initiate, we are seeking a new colleague to join the glepaglutide team.
The successful candidate will be:
- Responsible for designing, planning, conducting and reporting of clinical trials
- Responsible for coordinating collaborations with CROs and leading contract negotiations with CROs
- Responsible for risk assessment of the clinical trials and the development of sponsor oversight plans
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
Make a difference in a fast growing biotech company
As Director Downstream Manufacturing at Ascendis Pharma the main success criteria is to participate in building up the function in Product Supply, to assure a smooth tech transfer from Development to Commercial Manufacturing and to establish close and high-standard cooperation with the CMOs used by Ascendis Pharma.
The Director Downstream Manufacturing reports to the Senior Director Drug Substance Manufacturing and will be part of a very dedicated and experienced team.
For a Phase 3 project, the Director will be drug substance responsible (downstream) for the commercial manufacturing process and will be responsible for outlining pre-launch activities, post PPQ activities at the CMOs manufacturing intermediates and drug substance.
As Clinical Trial Manager, you play a key role with responsibility for planning and conducting external clinical trial activities with focus on BAHS sound processors and audiological aspects to help us ensure that our clinical documentation meets relevant requirements and standards.
Moreover, you will be involved in further improvements of the internal processes and procedures for clinical documentation and clinical trials.
Summed up, you will be responsible for the following tasks:
- Design clinical trials within the area of BAHS sound processors and audiology
- Write study protocols and case report forms
- Write documentation for study approval by ethical committee and competent authorities
The Danish Hydrocarbon Research and Technology Centre (DHRTC), Technical University of Denmark (DTU), invites applicants for a PhD position on characterization of complex hydrocarbon samples as a part of a project portfolio relating to investigations of enhanced oil recovery mechanisms in mature carbonate fields
DHRTC was established by the Danish Underground Consortium and DTU in 2014 as part of a national strategy for energy, the research centre is an ambitious, targeted effort to improve and sustain recovery of hydrocarbons from the Danish North Sea sector.
The position will be an integrated part of the fluid characterization work ongoing at DHRTC which focuses on targeted and non-targeted analysis of petroleum fluids by chromatography and mass spectrometry and water analysis.
DuPont Nutrition Biosciences ApS, Brabrand
Vil du være en del af et internationalt team, der arbejder med banebrydende enzymløsninger til foderindustrien?
Vi arbejder med kolleger fra hele verden og vores kunder er ofte store globale virksomheder. Vi har engagement, kompetence og erfaring indenfor enzymologi, biokemi og enzymers funktionalitet og skaber nye muligheder for kunderne hver dag.
Dine primære opgaver omfatter:
- Aktivitetsbestemmelse af enzymaktivitet i dyrefoder
- Evaluering og rapportering af forsøgsresultater
- Betjening og vedligehold af laboratorieudstyr
LM Wind Power, Lunderskov
Do you want to contribute to the continued success and growth of our Engineering Test and Validation Center, Manufacturing and Development by driving quality and continuous improvement of our Test and Validation Centre, Manufacturing and Development?
Based in our location in Lunderskov, Denmark, you will be part of the global Test and Validation Center, Manufacturing and Development, and lead the global team of 3-4 employees, responsible for development and management of our accreditation, ensuring zero defects supplies to our customers and implementing and continuously improving a LEAN operating system in TVC Manufacturing and Development. In the role, we expect you to:
- Lead your team and continuously motivate to improve efficiency and results.
- Drive and implement LEAN & Brilliant factory concepts in TVC Manufacturing & Development.
- Ensure quality control.
Unique Human Capital, Hvidovre
Erfaren og forretningsorienteret Pharma profil søges til Executive Search/Search & Selection
Med opkøbet af Flensby & Partners og Hedegaard Management i 2018 har Unique Human Capital fået øget volumen, og den strategiske plan for vækst gennem opkøb er nået. Dette betyder et stigende aktivitetsniveau, og vi søger derfor en erfaren Senior Konsulent med bred erfaring fra den pharmaceutiske industri, der sammen med et stærkt team kan sikre et fortsat højt fagligt niveau og en sikker linje i opgaveløsningen over for vores mange og alsidige pharma kunder.
Som Senior Konsulent hos Unique Human Capital vil du få en grundig indkøring til UHC’s processer ved at arbejde på den eksisterende Pharma og Biotech kundeportefølje og servicere vores nuværende kunder bedst muligt inden for vores kernekompetencer Executive Search samt Search & Selection.
LM Wind Power, Lunderskov
Our team in the Materials and Processes department is looking for a new talent to add to our expertise in surface coatings. Together with a team of experts, you will be improving and qualifying our blade surface material technology base and the associated coating application processes.
Lead small-scale projects, defining and executing strategy for blade surface coatings:
- Maintain and qualify surface coating material and application specifications and associated documentation
- Collaborate with our LM material testing lab in verification and validation of surface coatings and application processes
Orphazyme A/S, Copenhagen
Are you our new Science Writer? This is your opportunity to join a dedicated team of professionals and become an important part of the research department of a progressive and innovative biopharmaceutical company. Orphazyme A/S develops paradigm-changing drugs for the treatment of severe, debilitating neurodegenerative and neuromuscular diseases such as amyotrophic lateral sclerosis (ALS), sporadic inclusion body myositis (sIBM), and lysosomal storage disorders (LSDs).
We are seeking a Science Writer who can lead our soft-funding activities and support our scientific communication towards both professional and lay audiences.
- Leading our soft-funding activities
- riting scientific articles for publication in top academic journals
- Reading and researching specialist media and literature for internal strategic reporting
Thermo Fisher Scientific, Roskilde
Do you thrive in a dynamic, international leading company, and are you motivated by improving ways of directing and developing regulatory affairs? Are you committed and self-driven, and would you like an influential role where you will be enhancing performance whilst applying your Regulatory expertise within Medical Devices? Then you may be the one we are looking for.
We are now looking for a Regulatory Affairs Manager with real integrity and can-do-attitude to assume responsibility for the development as well as setting the direction within the regulatory affairs.
As Regulatory Affairs Manager you will be key in the development of the regulatory strategy for Roskilde and Europe, and at the same time provide RA guidance and support to ensure continued accuracy and compliance with international standards, internal procedures, applicable regulatory and legislation.