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Radiometer Medical ApS, Brønshøj
Do you remember why you chose to be an engineer? The urge to create perhaps or the passion for technology? At Radiometer creation and technology is the center of our business. We design, develop, manufacture and distribute world class Medical Devices globally.
We are looking for engineers looking to learn and apply their skills starting in September 2018 and for a duration of 20 weeks. Depending on the area of your interest, we try to find a relevant opportunity in parts of the organization where you have the chance to see the area of engineering in Radiometer Medical that fascinates you the most.
Furthermore, we are also interested in you if you are looking for a student assistant position and have more than 1 year left of your education.
We are looking for an experienced academic for a new position in Analytical Development, that will provide scientific leadership and coordination for analytical development activities. The department is part of Chemical and Pharmaceutical Research (CPR).
You will be responsible for the analytical development in our global development projects within our highly integrated CMC project organization. You will lead the analytical development for small molecule API’s and IMP for clinical studies, and ensuring sufficient quality of release and stability analyses, and coordination of project activities across the organization.
Unique Human Capital recruiting on behalf of Zealand Pharma in Glostrup
Work with QA in a fast growing and exciting biotech company
As QA Manager – CMC at Zealand Pharma you will become a part of the QA organization overseeing all activities and delivering professional quidance to ensure GxP compliance within all areas. You will be responsible for the overall QA oversight for one of the current phase 3 products applying your knowledge within GMP. The department is headed by the Vice President, Head of QA, and in addition to this position, encompasses 7 QA colleagues. You will be reporting directly to the Vice President, Head of QA.
Your key responsibilities
- Employ GxP QA expertise during the development providing GMP compliance guidance to internal stakeholders
- Influence the compliance of projects and programmes
- Review and approve internal and external documentation
Systematic A/S, Aarhus
Vil du gerne gøre en forskel og være med til at udvikle den elektroniske patientjournal i Columna Clinical Information System? Har du erfaring med Java og Android? Så har vi jobbet til dig.
Systematic har i flere år bidraget til digitaliseringen af sundhedssystemet, f.eks. ved hjælp af vores kliniske informationssystem, Columna, der samler alle relevante oplysninger om patienten ét sted og udgør en komplet integreret it-arbejdsplads for klinikeren.
Som softwareudvikler på Columna CIS vil du arbejde tæt sammen med kunden og have mulighed for at gøre en forskel for alle brugere af systemet, dvs. læger og sygeplejersker. Du bliver en del af et agilt og selvkørende team med dygtige kolleger, hvor du vil være involveret i en bred vifte af udviklingsrelaterede opgaver.
A position as data manager within the Integrative Systems Biology area lead by Professor Søren Brunak is to be filled as soon as possible. The position is time limited until January 31, 2019.
The position will require the candidate to lead, facilitate and coordinate data acquisition and data management procedures for both the IMI funded DIRECT and the ‘Danish Next Generation Sequencing and Bioinformatics Platform for Precision Medicine’ projects.
The appointed candidate will also be acting as a management interface between the group’s scientists and DTU’s High Performance Computing team, Computerome. Therefore, experience with systems administration, secure private cloud environments, MySQL, and programming (eg R, Perl, Python) is desirable. Experience with eCRFs and data handling is also desirable.
We are offering a job opportunity for a motivated professional to join a small team, which supports Global Pharmacovigilance & Clinical Development (GPCD) and ensures that we stay in compliance with internal and external requirements. Are you ready to bring your GCP knowledge and skills to an analytical level ensuring that our organisation is supported and maintains a high level of Regulatory compliance?
Fields of responsibility
- Provide GCP and other relevant Regulatory advice and support to GPCD
- Support GPCD with maintenance and continuous improvement of the QMS and the training system
- Act as project manager on relevant updates to the QMS and support GPCD where relevant in writing Quality Documents.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
High degree of influence in an exciting and fast growing biotech company
The Process Manager will work closely with the Global Clinical Development team leading/supporting the process changes, updates and compliance, and R&D operation's strategic directives. You will do that by ensuring the development and management of processes that enable compliance and standards across departments and apply best in class methodologies.
You will also drive global process improvements projects and support ongoing evaluation. You will lead the creation and maintenance of our processes – including but not limited to SOPs, guidelines, written instructions and other documentation processes. You will also ensure adherence to applicable guidelines/regulations.
As Process Manager, you will be responsible for effective implementation and creation of training sessions.
GE Healthcare Danmark A/S, Brøndby
Can you sell medico-technical products and do you have a clinical background/understanding? Then we need you as an Account Manager within Life Care Solutions for Zealand, Funen or Jutland.
You will be a part of the Danish and Nordic Life Care Solution teams with close contact with colleagues and support functions within your area.You will be responsible for budget within your area and will be developing strategies for different types of accounts to optimize sale and be able to maintain and develop your customer portfolio.
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 Clinical Pharmacology 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 cross functionally. 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.
We are searching for a graduate who can support Quantitative Pharmacology in the daily work and help us in our mission to become a world class pharmacometric service provider for Lundbeck.
Are you looking for the next step to kick-start your transition from an early career in clinical practice to become a young professional within Clinical Development in a leading pharmaceutical company within brain disorders? 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 you will encounter many exciting challenges cross-functionally. 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.
Are you looking for the next step to kick-start your transition from an early career in clinical practice to become a young professional within Clinical Development in a leading pharmaceutical company within brain disorders?
Symphogen A/S, Ballerup
The position as (Senior) Drug Product Scientist offers a unique possibility to take part in the de-velopment of Symphogens antibody products. You will mainly be responsible for drug product process development and manufacture from early stage IMP manufacturing and later stage manufacturing including process validation strategy.
You will collaborate closely with staff from our CMC group and in project teams, to ensure de-velopment progress of Symphogen’s antibody lead candidates.
Tasks and Responsibilities:
- Tech transfer of manufacturing processes to CMOs
- Technical responsible for drug product manufacturing documentation
- Ensure implementation of drug product manufacturing strategy between projects
CMC Biologics A/S, Søborg
Are you passionate about QC in Bioassay? We are looking for one additional scientist! Join a dynamic and international company where everyone is responsible for delivering right on time as one team!
As a Scientist in QC Bioassay, you will be responsible for delivering scientifically sound and cGMP compliant analytical results and documents, plan and complete various projects within deadlines in close collaboration with your colleagues in the group and assist the whole QC department with your professional expertise. You will also have direct contact with external customers and represent QC at regular customer meetings.
The main tasks are as follow:
- Write and review cGMP documents (e.g. test methods, general procedures).
- Review and approve analytical results for cGMP compliance and scientific content.
- Assist in analytical methods transfer from Analytical Development or customers into QC
Ferring Pharmaceuticals A/S, København
Would you like to join us in a challenging position as Clinical Trial Manager (CTM)?
Clinical Operations is responsible for planning and execution of clinical trials in phases 1 to 4 within all therapeutic areas in Ferring Pharmaceuticals. High quality trial data and adherence to timelines are important for us. To optimize the achievement of this, a good and constructive teamwork and strong leadership abilities in accordance with our values, are critical success factors.
Are you ready to manage Clinical Trials in an international environment? We are looking for a Clinical Trial Manager to effectively plan and oversee the assigned clinical trials as part of international trial teams. As part of the Global Clinical Operations team, you will work in an international environment with approx. 50 dedicated and highly skilled colleagues.
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
Zealand Pharma A/S, Glostrup
Zealand Pharma A/S (Zealand) is looking for an experienced patent attorney to join the IP Department, which presently counts two patent attorneys and one assistant. Key responsibilities will include building up IP strategies, patent application drafting, filing and prosecution together with patent search and analysis.
Zealand has built a large and diversified patent portfolio, and considers protection of inventions in peptide drug discovery and development to be key to our business success.
We offer a combined salary package including pension scheme and health insurance, as well as the option of joining the company lunch program, and use of massage, fitness and social facilities.
Vi søger en projektsygeplejerske til en stilling på 37 timer/uge med 18 timer til varetagelse af forskningsrelaterede opgaver og de resterende timer til almindeligt klinisk arbejde i medicinsk gastroenterologisk ambulatorium. Tiltrædelse 1. maj 2018 eller efter aftale. Forskningsdelen af stillingen er eksternt finansieret og indtil videre tidsbegrænset for en 2-årig periode.
Vi kan blandt andet tilbyde et job, hvor du er en vigtig del af afdelingens forskningsprofil. Dit arbejde består bl.a. af at
- identificere og kontakte mulige projektdeltagere
- varetage informationssamtaler med mulige projektdeltagere og deres pårørende under delegeret ansvar fra de projektansvarlige læger
- tilrettelægge og booke projektdeltagerens aftaler
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.
Hays Specialist Recruitment A/S recruiting on behalf of MSD in Copenhagen
Join MSD’s vaccines team and improve public health through partnerships and omni-channel customer engagement.
The Customer Manager Vaccines is the primary commercial point of contact in a designated area of vaccines and is accountable for the customer experience, coordinating internal resources and personnel to meet the needs of the customer.
In this role, you will 1) Develop long-lasting relationships with relevant specialists at hospitals and private clinics and identify and execute on opportunities for collaboration to improve public health and 2) Work closely with the regional organization to adapt & localize the brand strategies and ensure omni-channel customer engagement, including digital initiatives and appropriate non-promotional and promotional material.
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).