52 job matcher din søgning
Amgros I/S, København
Har du en sundhedsøkonomisk uddannelse, og er du motiveret for et job, der giver lidt mere mening end de fleste andre steder? Hvis ja, er det nu, du skal læse videre. I Amgros sikrer vi de offentlige danske sygehuse den rette medicin og det rigtige medicinske udstyr til den rette pris, på rette sted, til rette tid og i rette kvalitet. Som sundhedsøkonom har du en meget vigtig rolle i det arbejde. Du kan samtidig se frem til at komme ind i et super stærkt sundhedsøkonomisk team, hvor du vil få alle muligheder for sparring og faglig udvikling.
Dit primære fokus bliver sundhedsøkonomiske analyser, der skal give Medicinrådet de bedst mulige forudsætninger for anbefaling af nye lægemidler. På den vis har din indsats meget konkret og direkte effekt på det danske sundhedsvæsens udgifter – og for de patienter, der får mulighed for bedre behandling via bedre lægemidler.
LEO Pharma, Ballerup
Are you ready to play a key role in further advancing our 3D skin model platform?
You will join a small and agile team of highly skilled, dedicated and experienced Technicians and Scientists within cell/skin biology and immunology who are responsible for all 3D skin model pharmacology studies at LEO Pharma.
As a technical expert you can look forward to help shape and drive our continued development of predictive skin models in an environment based on trust and empowerment – your ideas are highly valued and you can expect full support to ensure your on-going development.
Your primary tasks will be to:
- Explore and establish innovative skin disease relevant 3D models to support our translational platform and contribute to specific projects
- Stay updated on new enabling techniques and systems, such as bio-supports, micro-fluidic systems, organ-on-a-chip and stem cells, and introduce relevant opportunities to the team
AGC Biologics A/S, Søborg
Our Project Management team is looking for an experienced Project Manager or Senior Project Manager for our Copenhagen office.
The Project Manager leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team and business development team. This role provides program direction and manages timelines and project controls across internal functional and organizational lines as well as with external clients.
As Project Manager/Senior Project Manager your responsibilities will be:
- Provide necessary program direction for planning, organizing, developing and integrating projects across multiple functional areas.
- Closely monitor/control project progression to ensure project is completed on schedule and within budget.
- Reports project progress to all key stakeholders.
Symphogen A/S, Ballerup
The position as Senior Downstream Scientist offers a unique possibility to take part in the CMC development of Symphogen´s products and participate in shaping the path for late stage development of our antibody mixture products in the Purification and Product Supply Team.
The Senior Downstream Scientist will be responsible for execution of process development of our products in clinical development including tech transfer to external CMO. In particular, the main tasks will be the downstream scientific lead for late stage development including process characterization and process validation activities for Symphogens most advanced projects.
In this position it is possible for the right candidate to participate in defining the late stage development platform and collaborate closely with staff from our CMC group and with the project team, to drive development progress of Symphogen’s antibody lead candidates.
Symphogen A/S, Ballerup
The Business Development Manager will be part of a small productive and agile global business team responsible for all aspects of deal making related to Symphogen’s assets including analysis and forecasting of market opportunities, financial modelling, outreach to pharma/biotech, due diligence, negotiation and alliance management.
As a team member, you will manage activities to identify, analyze and enable potential partnering opportunities and to support, maintain and grow working relationships with Symphogen pharma and biotech partners. You will be responsible for conducting competitive analysis, market forecasting and financial business modelling. You will collaborate closely with key internal and external stakeholders and be part of cross-functional project development teams for select drug candidates in early clinical and preclinical development.
Arla Foods, Videbæk
Can you apply your microbiology knowledge to production processes of milk-based powder ingredients? Then join the Deploy Team in Arla Foods Ingredients (AFI) R&D department. AFI is an independent company within the Arla Foods group, with the ambition to become a global leader in added-value whey.
Based in Nr Vium, Denmark, you will work among 75 innovators, research specialists and pilot plant technicians to “discover and deliver all the wonders whey can bring to peoples life”. Your ongoing mission will be to support the development of new processes for dairy based ingredients in powder form, and scale up from pilot plant units through to production. Among your stakeholders, you will work closely with Supply Chain, Quality, and Microbiologists from the Arla Foods Innovation Centre.
Are you motivated by challenging projects in the field of HVAC operations in a GMP environment? Do you have experience with connecting new technology to an existing plant? Do you take professional ownership for technical solutions and timely completion of documentation?
We are looking for a skilled and enthusiastic HVAC engineer to work within the field of production support in a change-oriented company. You will take ownership for the HVAC supply to API- and aseptic production facilities at our site in Hørsholm.
- An exciting and challenging position in a global pharmaceutical company, which is world leading within its field.
- Dedicated colleagues with an open and informal culture.
- A positive work environment with focus on cross-functional cooperation.
Brinch & Partners is recruiting on behalf of Particle3D on FynChief Executive Officer
Life science – Start up – Operational
You will take over the overall responsibility of the company and will be working in close cooperation with the board of directors, the founders and other stakeholders. You will be building a commercially viable business model based on a very promising technology and several years of research.
Your focus will include business development, clinical tests, project management, fundraising, stakeholder management, sales and operations. You will lead a small internal team and work together with several external consultants and partners.
One of the first major objectives will be to create a go-to-market strategy as well as making sure that the clinical tests are executed as planned.
LEO Pharma, Ballerup
If you have solid experience across bioanalytical assays and biomarkers, and you are looking for a job with major freedom to perform and massively impact in a cross-functional project driven environment, we have the perfect job for you. LEO Pharma has set the very ambitious goal to become the world’s preferred dermatology care partner.
As Principal Scientist in our Preclinical Development team you will have two main focus areas: bioanalytical assays and biomarkers – and you will become your team’s primary expert within biomarkers. At LEO we use CRO's to handle development of drugs meaning that your role is to set up, lead and monitor studies at CRO's, rather than being in the lab conducting experiments on your own.
LEO Pharma, Ballerup
If you have a solid understanding of guidelines across EMA/ICH/FDA, and you are looking for a job with great variety of tasks and global vision, you don’t have to look any further. At LEO you will be part of a successful and rapidly growing company, and you will join a well-functioning department known for team spirit, cooperation and genuine care for each other.
Strong pharmacovigilance (PV) is important for LEO, and as we are growing globally, our area of expertise – and your presence – becomes yet more important. As Senior Pharmacovigilance Specialist your primary focus is to make sure that overall processes are maintained and optimised in order to submit/distribute case reports according to PV legislation and maintain a high compliance in relation to legislation worldwide.
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to be part of a great, growing team responsible for global safety surveillance of Ferring’s portfolio within reproductive health and gastroenterology? Do you thrive in an international environment of great change where you can influence the surroundings? Do you like to work both with post-marketing and clinical activities?
As Pharmacovigilance Manager you will play an important role in leading drug safety for a key area of Ferring’s portfolio working as an integrated member of a highly motivated and dedicated team collaborating with clinical development, regulatory affairs, affiliates and partners for assigned products/projects.
Your essential tasks include case processing, post-marketing safety surveillance, safety reports and safety handling in clinical trials in collaboration with Pharmacovigilance Physicians.
Zealth ApS, København
Zealth vokser, og vi søger en ny medarbejder til vores team. Vi søger en Healthcare Consultant, der ønsker at arbejde i et iværksættermiljø - I en virksomhed, hvor nøgleordene er kundefokus, teamwork og fokus på at skabe resultater.
- Supportere medicinalvirksomheder med deres ansøgning til Medicinrådet
- Udvikle materiale og kommunikation rettet mod læger og andet sundhedsfagligt personale
- Udvikle træningsmaterialer til brug for intern træning hos medicinalvirksomheder
Zealth er en konsulentvirksomhed med fokus på sundhedssektoren. Vi arbejder bl.a. med market access, marketing og medicinsk kommunikation, projektledelse og organisationsudvikling.
Coloplast A/S, Humlebæk
Join Coloplast to become part of a global company that makes a difference every day.
You will work from our Headquarter in Humlebæk, Denmark. Here, you as a senior specialist will ensure appropriate and compliant biocompatibility documentation for Coloplast products applying your insight into regulations and industry trends. You will help grow the team by acting as a mentor through guidance and coaching of junior colleagues, especially with respect to scientific and professional aspects of evaluation of biocompatibility and toxicology.
In addition, you will provide expert toxicological support to the business, initiating and monitoring biocompatibility testing in-house as well as with our suppliers. Supporting cross-functional activities related to biosafety, you will influence our policies, guidelines and attitudes regarding environment and safety for our customers.
Do you have drive and a well-founded experience with Supply Chain Management and Pharma?
With reference to the Nordic Supply Chain Director, the Sourcing Manager executes the assigned category strategy and is responsible for executing or supporting strategic sourcing activities to include benchmarking, supply market analysis, supplier analysis, RFI/RFP building, negotations, baseline analysis, contracting, outsourcing & offshoring, product lifecycle management, and building business cases.
Examples of more specific key responsibilities:
- Periodic audit of supplier invoices
- Manage stakeholder relationships
Danpo A/S, Aars
Som sidestrømsansvarlig kan du se frem til en spændende rolle i vores nyetablerede organisation, Scandi Ingredients, der har fokus på udvikling af sidestrømsprojekter på tværs af enhederne Produktion, Salg og Udvikling.
Organisationen arbejder for at sikre fremtidens udvikling inden for sidestrømme samt med kommercialisering af potentialet. Mere konkret beskæftiger du dig med at:
- projektlede – igangsætte udviklings- og optimeringsprojekter
- følge op på projekter samt performance og udbytte
- sikre dokumentation.
Ferrosan Medical Devices A/S, Søborg
Ferrosan Medical Devices A/S har haft en imponerende vækst de senere år og det stiller store krav til vores drift, produktions- og produktudvikling. Til at lede nogle af vores komplekse og tværorganisatoriske projekter søger vi en projektleder.
Som projektleder bliver du en del af Project Execution Unit, der er en gruppe af dygtige projektledere, som leder tværorganisatoriske projekter, indenfor eksempelvis produktudvikling, produktændringer, kapacitetsudvidelse og compliance.
Projekterne er i varierende størrelse og omfang og varer typisk 1 til 4 år. Du vil normalt arbejde med 1-2 projekter ad gangen. Du vil bl.a. have ansvar for etablering og overholdelse af tids- og ressource planer, projektøkonomi, og for at styre projektets samlede leverancer fra start til det er fuldt implementeret i drift.
- robust og empatisk leder med fokus på effektivisering
F10 Human Resource søger for LEO Pharma A/S
Hvad siger du til en spændende stilling, hvor du får mulighed for at bidrage med dine kvalifikationer, erfaring og menneskelig indsigt til at implementere LEAN samt styrke motivationen og tilfredsheden i din afdeling?
Har du tidligere arbejdet med GMP og steril API, og er du uddannet farmaceut, kemiingeniør, Cand. Scient. biokemiker eller lignende?
Hvad siger du til at være en del af en verdensomspændende organisation, hvor frihed under ansvar samt udvikling er sat i højsædet?
Vi ser frem til at modtage din ansøgning ref.: 8021
LEO Pharma, Ballerup
Biopharmaceutical Products are looking for a formulation scientist for late stage development and implementation support to monoclonal antibodies drug products.
LEO is taking over increased responsibilities from external collaborations and to accommodate this change We are ramping-up to late-stage CMC drug product capabilities. Being part of a late stage project team is a unique opportunity to be pioneering within biologics at LEO and to build relationships and working experience for externalised projects.
Collaboration with external manufacturing and development partners and provide subject matter expert support on an ongoing basis. This also includes some travel activities for face-to-face meetings and on-site participation. Write and/or review protocols and reports, including regulatory module 3 sections.
LEO Pharma, Ballerup
If you have project management skills acquired from working with medical device development and you are looking for a job, where you can unfold everything you know and have major impact, this is your chance. At LEO Pharma you will join a small and agile team in the beginning of the company’s highly prioritised journey within device development.
As Technical Project Lead you will spend most of your time managing technical development activities. You will create project plans of your own as well as reviewing plans in order to evaluate coherence and realism. As part of this you will use your design control experience to assess risks. Additionally, you take ownership of submissions to authorities like FDA and EMA.
LEO Pharma, Ballerup
LEO Pharma has set the very ambitious goal to become the world’s preferred dermatology care partner. To make this vision come true we are taking our organisation to the next level. And that is why we need you and all of your good quality DNA.
As Quality Specialist your overall focus is to ensure top quality in deliverables from external partners. You will become key player in handling the daily operation in an area of great (and exciting) complexity. You will have multiple contacts on a daily basis and be trusted to make business critical decisions on your own.