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LEO Pharma, Ballerup
Can you ensure compliance in our electronic document management system?
MyDoc LEO is the repository of approx. 17.000 strategic and operational procedures, and your focus is to facilitate compliance for the G3M and HR part of those. A vital part of the solution is to manage the training and to ensure documents are frequently reviewed – in order to be in compliance with various regulations and uphold our License to Operate. Related to the theoretical training, you will interact with the Department Managers and assist in building and maintaining training matrixes and to secure that the employees receive the correct documents for training. Your primary tasks will be to:
- Provide end-user support – via mail, telephone and face to face in Ballerup
- Establish and maintain training matrices
- Distribute documents for training to end-users
The CoaST Research Centre at DTU Chemical Engineering seeks qualified candidates for Post Doc positions in new fields of functional coatings and testing methods.
The activities in CoaST cover coating technologies from raw materials, over formulation, test and characterization to production and application.
In the broad perspective, the center will support development, production and use of high performance coatings with improved sustainability profiles over the lifetime of the coating.
Antimicrobial resistance (AMR) is one of the largest threats against global health and obtaining information about the global prevalence and emergence is essential to guide interventions.
The Research Group for Genomic Epidemiology at the Technical University of Denmark, DTU, is together with several partners worldwide trying to understand the global emergence of infectious diseases and antimicrobial resistance mainly based on metagenomic sequencing of samples from multiple reservoirs.
As part of this global endeavour, we have recently participated in the identification and global characterisation of a number of the largest bacteriophages which have not been discovered before. To isolate, identify and study the biology of these bacteriophages more closely we are seeking a research assistant to help with laboratory work.
Coloplast A/S, Humlebæk
Til afdelingen Surface & Film Materials, en underafdeling af R&D materialeafdelingen, Materials, søger vi en engageret og dygtig laborant/laboratorietekniker. Technology er en del af Coloplasts Global R&D-afdeling og har til huse i hovedkontoret i Humlebæk. Vi er mere end 120 medarbejdere i Technology, der arbejder dedikeret med udvikling af produkter, som forbedrer livskvaliteten for vores brugere, primært inden for Coloplast Chonic Care, Stomi og Kontinens.
Som laborant får du:
- En dynamisk hverdag, hvor du vil være med til at gøre en forskel, i en åben og uhøjtidelig atmosfære.
- Tæt samarbejde med minimum én specialist, som du vil deltage i produktudviklingsprojekter sammen med. Sammen har I ansvaret for at udvikle og identificere de bedste materialeløsninger til projektet.
- Under projektforløbet har du ansvaret for at skulle teste, evaluere og dokumentere resultaterne, så der kan træffes databaserede beslutninger i projektet.
The Research Group for Genomic Epidemiology, has the primary task of conducting targeted research with the aim of predicting and preventing infectious diseases in humans and animals, and supporting detection, surveillance and control. The research group is an EU reference laboratory for antimicrobial resistance.
The Research Group for Genomic Epidemiology host a number of internal and external bioinformatics pipelines, that are widely used for analysing whole genome sequencing data as well as whole community sequencing data.
The research group seeks a highly qualified and dedicated bioinformatician/database manager who can ensure that all pipelines and databases are keeps functionally and updated and who can address questions and contacts from internal and external users.
Nuevolution A/S, Copenhagen
Nuevolution is dedicated to the identification and development of novel drug programs addressing unmet medical needs with a main disease focus on Inflammation and Oncology.
You will be part of multiple Nuevolution drug discovery teams taking projects from hit discovery through lead optimization to candidate selection. You will work as a Research Assistant in the Hit Synthesis Group.
Common tasks include:
- Synthesis of multiple small molecules in parallel on 2 micromole scale both using solid-phase organic synthesis (SPOS) and parallel solution-phase techniques
- Record and interpret analytical data, e.g. HPLC/MS, UV, and CLND
- Optimize the reaction conditions presently used and develop new reactions for a parallel setup
The Department of Bioengineering and Biomedicine at DTU, Technical University of Denmark, invites applications for a position as professor in integrated micro- and nanotechnological systems for biological and biomedical applications with focus on research and innovation.
The successful candidate is expected to lead an international competitive research group focusing on the development of highly sensitive and reliable point of use (POU) technologies with specific emphasis on microorganisms in medical diagnostic, treatment, and monitoring as well as in environmental monitoring. It is also expected that the research has focus on applying physics in biological systems to separate and differentiate biological structures to monitor biological processes and to optimize growth, nutrient delivery, and waste removal in cellular and bacterial cultures.
A Postdoc position is available at the Section for Protein Chemistry & Enzyme Technology. Research in this section aims to attain new knowledge within protein- and enzyme-structure function relations, enzyme-substrate interactions, biocatalytic mechanisms, energy relations and kinetics, and on enzyme-protein robustness and stability.
The main theme of the work will be rational enzyme design. This will involve thorough kinetic characterization of enzyme activity on insoluble substrate as well as analysis and mathematical modelling of the results. The project has special focus on relationships between substrate binding strength and catalytic efficacy, and this includes analysis of so-called Linear Free Energy Relationships and application of the Sabatier Principle.
Chr. Hansen A/S, Hørsholm
In our Stability & Technology department you will reinforce the existing team of 7 competent and engaged colleagues working in a creative environment. The department cooperates with customers, colleagues, universities and research institutes both nationally and internationally.
This is an outstanding and unique scientific position where your responsibilities will count:
- Set the standards for formulation technology of bacterial cultures at Chr. Hansen
- Formulating and stabilizing bacterial cultures for multiple applications
- Conducting downstream processing studies, validation activities, and characterization activities of biologic products
We work in cross-functional projects, therefore responsibility, engagement and team playing are core values for you – as it is for us
We are looking for a Principal Scientist with a strong research background in psychiatric disorders and molecular biology training to join the Lundbeck Research Neuroscience organization in the department for Signal Transduction. As part of the larger Lundbeck R&D organization, we are focused on utilizing molecular and cellular neuroscience to establish the pharmacodynamic mechanisms of drug candidates at the cellular level and to continuously develop our understanding of disease biology and therapeutic entry points.
Your job and key responsibilities
- With your in-depth understanding of psychiatric disorders and with your firm grasp of genetics, molecular and cellular biology you will contribute with scientific leadership and key experimental data to guide and ensure the progression of drug discovery projects.
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? Then you might be the new colleague we are looking for.
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 a key 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
The Danish Government and Danish Regions launched the National Strategy for Personalised Medicine 2017–2020 in December 2016. The strategy creates the foundation for a balanced development of personalised medicine in Denmark for the benefit of patients – now and in the future. The National Genome Center (NGC) will serve a key role in the realisation of the strategy.
The Chief of the national WGS Center (CWC) is a part of the executive team at the National Genome Center.
With reference to the CEO, the CWC is responsible for the operation of the National WGS Center including planning, coordination, quality assurance and development in accordance with the objectives and goals set for the National WGS Center.
The Center for Microbial Secondary Metabolites, CeMiSt, is a Center of Excellence funded by the Danish National Research Foundation. The Center started 1st of January 2018 and will run for six years with an option for a four-year extension.
We are looking for an ambitious mycologist with a broad experience in fungal ecophysiology, genetics and secondary metabolite production.
You will get a unique possibility to work on fungal (and bacterial) ecosystems focusing on how secondary metabolites of terrestrial fungi affect microbial diversity and functionality in both natural and engineered systems.
Arla Foods, Viby J.
Are you passionate about Food Chemistry? If so, join the Food Chemistry Team in Arla Foods. We have a global role in Arla R&D and are based in our Innovation Centre in Aarhus, Denmark.
You will be a key partner in innovative science projects and tasks with focus on protein chemistry. In this role you will combine your strong scientific skills with a business mindset. To be a success in this job you drive the protein chemistry link to a number of research and innovation projects and make sure they meet the expectations as to deliverables, time and resources.
In this job you will together with our R&D laboratory technicians maintain and develop our analytical competencies through method development and optimisation.
Pharmacosmos A/S, Holbæk
Pharmacosmos søger en dygtig QA-specialist, da vi ønsker at styrke QA-området indenfor GMP og GDP.
Med reference til Quality Director vil du indgå i et dynamisk team, der varetager alle opgaver indenfor QA-området, blandt andet batch review og frigivelse af produkter, vedligehold af kvalitetssystemet, audits og selvinspektioner, behandling af ændringssager, afvigelser og reklamationer, kvalificerings- og valideringsopgaver og tværgående projekter. Du vil få en varieret arbejdsdag med mulighed for at varetage opgaver, der passer til din profil.
Det vil være en fordel, hvis du har erfaring med følgende områder:
- Aseptisk fremstilling/fremstilling af lægemidler
- Batch review
VAR2 Pharmaceuticals ApS, Copenhagen
If you like to work in the international biotech business and become a significant contributor to the building of a young Danish company, this might be the job for you!
You will join a group of ambitious scientists that work hard to bring innovative new cancer therapies and diagnostic methods to clinical testing within the next couple of years. To succeed with our ambitions, we are now looking for a new colleague that can help us create the necessary infrastructure and progress development projects and other important activities according to our plans.
As Project Coordinator you will work closely with the management team and project groups. In this role you will primarily work with project management tools to support the entire organisation in both the planning and execution of the development projects as well as implementation and follow-up of management tasks and processes.
Y-mAbs Therapeutics A/S, Hørsholm
A new position is now open! Y-mAbs Therapeutics A/S (Y-mAbs) is looking for a CMC Project Manager. You will primarily focus on CMC activities associated with our late stage biologic development programs, and you will work with close interfaces to other functional groups within Y-mAbs. A good understanding of the outsourcing process, from quotations and contract negotiations to follow-up and troubleshooting with our CMC partners is a key competence as all manufacturing is outsourced.
It is key that you have in depth expertise within one of the following areas:
- Specific knowledge about drug product development in late stage development programs including commercial launch
- Formulation development of biologics – knowledge about sub-cutaneous formulations will be an advantage
- Solid experience in working with CMO/CRO's and international regulatory bodies like FDA and EMA
We are looking to add a new Senior Specialist with strong experience within upstream process development and manufacturing to our CMC Biologics team. The team is responsible for the strategic and technical leadership of pharmaceutical development activities in support of our biologics pipeline – spanning from pre-IND stage through process validation and launch.
As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.
Thermo Fisher Scientific, Roskilde
Do you enjoy creating results in a fast-paced environment, and do you want to be an important part of a strong commercial team working together to help our customers make the world a better place?
In this role you will maintain effective customer relations, develop opportunities for growth within an existing customer base, and assure market penetration and profitability while achieving sales and profit forecasts. You may be based in the greater Copenhagen area (Denmark) – or Southern Sweden.
Your further responsibilities among others will include:
- Meet or exceed business goals of our commercial targets for the territory
- Drive the tactical implementation of the business plan – including sales to new accounts, successful introduction of new products, and the retention of current customers
LEO Pharma, Ballerup
You will be Lead Auditor and will plan, perform, report and follow-up on audits. Are you a structured and systematic team player, who dream of a job with major responsibility and the license to impact decisions, you might be just the person we are looking for.
As our new Principal Quality Auditor, you will perform audits of LEO Affiliates, Regions and at our GXP regulated third parties. Audits is performed within GDP/GMP, PV and RA areas. LEO Pharma has more than 30 Affiliates in Europe, North America, South America, Middle East/Mahgreb, Asia and Australia. Each Affiliate/Region has GXP responsibilities towards QMS, distribution, pharmacovigilance, medical information and regulatory. It is LEO Pharmas responsibility from a corporate level to oversee the GXP compliance level through audits.