22 job matcher din søgning
Symphogen A/S, Ballerup
Symphogen is currently experiencing an increase in activities within both the early and late stage projects. Furthermore, Symphogen is planning to start phase III clinical trials and to apply for a Manufacturing and Import Authorization (§39 Licence).
Symphogen therefore plans to strengthen the QA organization with a Quality Manager.
As Quality Manager you will be involved in every step of the manufacturing process from generation of cell banks, upstream and downstream processes, final formulation, filling, analysis and release of the final drug product. The manufacturing is outsourced to various CMO's in EU and US.
The Quality Manager will participate for the quality group in our projects covering process and analytical validation, PPQ, clinical supply, and eventually marketing application.
FMC Corporation, Hørsholm
We are looking for a talented individual for our European Innovation Center in Hørsholm to assume the responsibilities as a Country Registration Specialist. In cooperation with Nordic, European and Global colleagues you will be a key contributor then growing innovation is a key mantra within the company.
In your role as Country Registration Specialist you will prepare, maintain and submit registrations for FMS’s protection products in the Northern Zone. The job includes multiple interactions with various types of stakeholders, as national authorities and institutes, local farmers’ organizations, customers, development colleagues and business teams. The tasks vary substantially from day to day, and multiple projects are running in parallel.
Biomatters ApS, Aarhus
Biomatters is seeking a highly motivated Key Account Manager to join our team in Aarhus, Denmark. The Key Account Manager will work in Europe and be responsible for strategic sales, management and growth of accounts, as well as all phases of the sales process. Along with closing business, your daily responsibilities will include uncovering and generating new leads, qualifying and converting leads into business opportunities, and delivering presentations.
The position requires the ability to meet challenges with resourcefulness, generate solutions for improving sales, and develop innovative approaches and ideas. The ideal candidate must have a fundamental understanding of genomics and related life sciences.
- Deliver closed business monthly to exceed assigned quota.
- Maintain accurate and descriptive accounts and accurate sales forecasts within our CRM (Salesforce).
Vi søger en bioanalytiker i et vikariat på 37 timer/uge i perioden 1/3-2018 til 31/12-2018. Stillingen er i histologien ved Klinisk Patologi, Vejle Sygehus, SLB.
Vi er ca. 20 histobioanalytikere, og vi håndterer årligt godt 30.000 histologiske prøver. Vores immunhistokemiske analyser er placeret organisatorisk i histologien, og vi deltager gerne i forsknings- og udviklingsopgaver. Som led i kompetenceudvikling/jobglidning har vi flere bioanalytikere med diplomuddannelse i udskæring, som dagligt varetager en del af den komplekse udskæring. Vi arbejder målrettet med høj faglig kvalitet i vores arbejde og har et patientcentreret fokus på svartider.
Vi er gode til at hjælpe hinanden på tværs af faggrupperne og er en rummelig afdeling, der giver plads til hver enkelt medarbejders faglige og personlige udvikling i en hverdag med mange opgaver.
As specialist in the Section of In Vitro studies you will join a group of one academic (Head of Section) and three experienced technicians to deliver in vitro toxicological support to early discovery projects. As an expert in in vitro methods and/or molecular toxicology we envisage that you will actively take part in developing and optimising our current high content screening methods and propose new in vitro and/or in silico screening strategies, when relevant.
A very exciting and dynamic research environment with experienced, collaborative colleagues. We are dedicated in our work and take pride in delivering high quality results and safety assessments that support research projects in the best possible way. The working atmosphere is informal and positive, offering good opportunities for collaboration and personal development.
Qiagen Gmbh, Aarhus
As a Product Owner at QIAGEN Aarhus, you will join a team that develops the world’s leading bioinformatics software solutions. The solutions are used worldwide by researchers within pharmaceutical, agro, biotech, clinical, and academic segments.
You will lead the development of key software products for NGS data analysis and take responsibility for the development of our versatile, scalable and user-friendly bioinformatics platform.
- Responsible for defining software requirements for state of the art NGS analysis software.
- Coordinate software changes with internal stakeholders.
- Ensure alignment with an international stakeholder portfolio.
Intomics A/S, Kgs. Lyngby
The Global Sales Specialist will be part of the Global Sales and Marketing Department, and will be involved in maintaining and developing Global Sales activities. You will be reporting to the VP, Sales and BD, but will be personally responsible for the majority of projects, you are handling.
Your main responsibility will be sales of software products and tailored big data analytics solutions developed for the pharma and biotech industry. You will also be responsible for analyzing market requirements to ensure, that our products and services continue to competitively meet or even exceed customer expectations.
Our products are aimed at various stages of the drug discovery and development pipeline such as biomarker discovery, target identification, drug discovery and patient stratification. The sales process will very often require an individual approach to the individual customer.
LEO Pharma, Ballerup
Do you want to be part of a global regulatory department with focus on labelling strategy and content for LEO’s global product portfolio? Do you want to help us ensure value-adding label with a patient-centric and market-access focus?
The primary responsibility of the Regulatory Labelling department is to manage all labelling-related activities including development and life-cycle activities from a strategic as well as operational point of view.
As a Regulatory Labelling Professional you will be a key person in driving the RA deliverables related to labelling activities e.g. lead the cross-functional establishment and maintenance of Company Core Data Sheet (CCDS) as well as EU SmPC/PIL for products authorised via CP and MRP/DCP.
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
In a fast growing biotech company
As QMS Manager at Ascendis Pharma, the main success criteria is to create a good understanding of QMS guidelines and procedures in order to support the different business areas. Ascendis Pharma has just launched a new cloud-based Electronic Document Management System (EDMS) and in cooperation with all functions across Ascendis Pharma worldwide, you will contribute with your knowledge within QMS to ensure compliance according to requirements. You will be part of a global QA team and become part of a very exciting journey taking Ascendis to the next level.
Your main responsibilites are:
- Drive the implementation of the QMS module of the EDMS
- Apply your experience and knowledge with Standard Operating Procedures in the establisment and implementation of Ascendis Pharma’s Quality System
- Design and implement global training processes
Bavarian Nordic A/S, Kvistgård
Would you like to fight Ebola and other life-threatening diseases focusing on batch release and deviations?
“You get to build on your knowledge and skills as part of a leading biotech company. Working with living virus, you ensure that our vaccines and medicine are safe and compliant. At the same time, you get to collaborate with specialists that are ready to share their extensive knowledge with you. Doing so, you get to work in-depth with biotechnological as well as aseptic production from start to finish”.
Stepping into Production Support, you join 20 academics in charge of introducing new products to our production, taking care of any occurrences that happen during production and handling all documentation afterwards.
On top of that, we are in charge of contact with key stakeholders, such as authorities and suppliers as well as maintaining documentation.
Er du drevet af at gøre en forskel for patienter og det danske sundhedsvæsen? Er molekylær diagnostik din spidskompetence? Motiveres du af at arbejde med innovation og ny teknologi?
Vi søger to dynamiske og engagerede Sales Application Specialists til vores salgsteam inden for patologi og mikrobiologi. Du bliver en del af et salgsteam på 20 personer, som har opgaver inden for salg, applikation og træning af vores kunder, primært på patologiske, mikrobiologiske, genetiske og immunologiske afdelinger på hospitalerne.
Dine primære opgaver:
- Produktsupport og undervisning af kunder og kolleger.
- Opsætning af applikationer indenfor patologi, onkologi, virologi, mikrobiologi og blodscreening baseret på qPCR/NAP og sekventering.
- Salg af testreagenser.
We are looking for a highly motivated Principal scientist to join our Drug Discovery department. You will be part of a team, consisting of skilled and engaged Discovery scientists who are responsible for driving Discovery programs based on the Locked Nucleic Acid (LNA) Drug Platform, in a variety of disease areas.
Your role will be to manage discovery projects within the RNA therapeutics technology area. To be successful in this position it is crucial to understand the environment in Biotech discovery programs. On a daily basis, you prefer to be hands-on with the research and at the same time to lead stakeholders in both internal and external lines through the process in accordance with defined plans and milestones.
Signium International Danmark recruiting on behalf of GSK Pharma in Brøndby
On behalf of GSK Pharma, we are looking for a Quality Lead to join the quality team in Denmark and Nordic Cluster – consisting of Denmark, Island, Finland, Norway and Sweden. The position is based in Brøndby in the outskirts of Copenhagen.
You will be responsible for the Quality oversight of GSK prescription medicinal products distributed in Denmark and Iceland. You will act as the Responsible Person of GSK Pharma in Denmark as defined by the European Good Distribution Practice (GDP) guidelines.
The focal point of the position is quality strategy and quality systems, covering all GDP (Good Distribution Practice) areas such as deviation handling, self-inspections/audits, change control, risk management, product distribution, third party management, as well as product complaints/defects/recalls.
En tidsbegrænset stilling på fuld tid som molekylærbiolog med interesse og erfaring indenfor genetik er ledig til besættelse i det molekylærgenetiske afsnit ved Klinisk Genetisk Afdeling, Vejle Sygehus i tidsrummet 16. april 2018 - 31. marts 2019.
Vi tilbyder et arbejde i et spændende fag med stort udviklingspotentiale, gode arbejdsforhold, og et veludstyret laboratorium.
Stillingen omfatter analyse af NGS og microarray data, samt resultater fra molekylærbiologiske undersøgelser som PCR, pyrosekventering og MLPA. Du forventes at medvirke til kvalitetssikring, svarafgivelse til vores kliniske rekvirenter, samt udvikling af nye analyser. Der lægges vægt på, at du har erfaring med basale DNA-teknikker, NGS og DNA microarray.
Symphogen A/S, Ballerup
An exciting scientist position is available within the Antibody Discovery department, offering a unique possibility to participate in the screening and characterization of our large therapeutic antibody repertoires, using state-of-the-art technologies. The ideal candidate holds a PhD in biochemistry, immunology or related discipline and a track record of high quality research.
Your main role will be to participate in flow cytometry based antibody screening, validation and FACS sorting, as well as affinity and epitope characterization using biosensors. As a scientist in Antibody Discovery (AD) day to day tasks include planning, generation, discussion, and presentation of results. A large degree of hands-on laboratory work is to be expected. You will ensure proper documentation of results and knowledge sharing within the department and in project teams.
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
Join a Fast Growing Biotech Company
As Senior Director of Quality Systems and Compliance at Ascendis Pharma, the main success criteria is to develop a high performing team, owning the company´s Quality System and driving it´s successful execution, as well as driving the company’s compliance programs including licensing and inspection preparedness.
You will be part of the Ascendis Pharma Quality Leadership Team and become part of a very exciting journey establishing a superior biotech Quality Organization for product development and CMO manufactured products.
Your main responsibilites are:
- Ownership of the company Quality Manual, Quality Metrics, and respective reporting to senior management
- Ownership of key systems like the Quality Documentation System, Training System, CMO qualification system, audit, and complainthandling
Molekylærbiolog søges til 3-årig stilling delt mellem Klinisk Genetisk Klinik, Rigshospitalet, og Børneonkologisk laboratorium,...
Region Hovedstaden, København
The Department of Biomedical Sciences, Faculty of Health and Medical Sciences at the University of Copenhagen is offering a position for a...
Biomedicinsk Institut, København
En fuldtidsstilling som molekylærbiolog ved MolekylærEnheden, Patologiafdelingen, Herlev Hospital, er ledig til besættelse pr. 1....
Region Hovedstaden, Gentofte, Herlev