26 job matcher din søgning
Compass Human Resources Group A/S recruiting on behalf of Sanofi Genzyme in Copenhagen
Sanofi Genzyme is one of the World’s leading Specialty Care pharmaceutical companies, focused on development of innovative therapeutic solutions in Immunology, Oncology, Multiple Sclerosis and Rare Diseases. Due to a strong pipeline and increased focus in the Immunology therapy area, Sanofi is right now looking for a skilled Field Product Manager for this newly established position and their upcoming launch of the first-to-market treatment of an IL4/IL13 for patients with severe Asthma.
As Field Product Manager, your responsibilities will include developing a personal customer network in Denmark among KOL’s, setting up relevant projects with HCP’s supporting the field based team to secure the overall commercial success of the launch of a very unique product with a huge recognized potential.
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.
Coloplast A/S, Humlebæk
Are you ready to kick-start your international career, supporting product quality assurance and regulatory compliance in a world-leading company? As one of two new quality graduates, you will either manage QA projects related to brand new products or ensure that existing products live up to the regulatory requirements of our global markets. Either way, you will learn to navigate a complex regulatory landscape and get a high level of autonomy to find the best solutions.
The Coloplast Global Graduate Programme is a three-year full-time programme. A talent programme for top students with a potential and drive for leadership.
The programme alternates between 18 months at our HQ in Denmark and 18 months in a global subsidiary or production site. During this time, we guarantee that you’ll get to dive into your field of interest, take on key responsibilities and see the results of your work.
Coloplast A/S, Espergærde
Do you have a bright and curious mind? And would you like to see your creative ideas turn into new innovative products for future full-scale production?
As process engineer, you participate in 1-2 new product development projects at a time to develop and define all production processes, e.g. identifying manufacturing equipment and methods. Ensuring efficient process scalability from pilot to high-volume production, you:
- Design processes and build prototypes in close collaboration with our designers, R&D and workshops
- Develop, document and verify process stability and scalability for new products ready for production ramp-up
- Follow up on results and create action plans, risk assessments and cost efficiency calculations
Senior Drug Substance Specialist
Zealand Pharma A/S, Glostrup
As our new Senior Drug Substance Specialist you will primarily be involved in late stage Drug Substance (synthetic peptides) as well as participating in research/early stage projects with focus on drug substance production.
The successful candidate will:
- Be involved in late stage drug substance development (PPQ activities and Risk Management) as well as participating in research/early stage projects
- Manage the collaboration with DS CMO (follow up on oversight plans and day-to-day communication, and securing transfer of knowledge)
- Contribute to risk assessments and CQA development at the CMO
The Department of Bio and Health Informatics at the Technical University of Denmark (DTU Bioinformatics) has its main research and teaching activities in bio-medical and bio-technological informatics, metagenomics, epidemiology, integrative systems biology and machine learning.
The research at DTU Bioinformatics is focused on bioinformatics and computational analyses of large amounts of data generated within biological, biomedical and biotechnological and life sciences area. We strive to gain new knowledge and drive innovation in human, animal, plant and food science and collaborate with all relevant industries.
The department is seeking an Assistant or Associate Professor. The position will be placed within DTU Bioinformatics and the candidate is expected to join one of the existing research groups.
Lead Statistical Programmer
Zealand Pharma A/S, Glostrup
We need a Lead Statistical Programmer who can establish a statistical programming function across all development projects at Zealand Pharma. You will be part of the Biometrics Department, currently consisting of 2 statisticians, which is responsible for statistics, statistical programming and data management. We help create and implement clinical development strategies, manage standards, and provide expert sparring to external partners.
The successful candidate will
- Develop and drive alignment of data standards and programming processes
- Lead programming activities with clinical trial and submission teams
- Establish a company data repository
Lead Data Manager
Zealand Pharma A/S, Glostrup
We need a Lead Data Manager who can establish a data management function across all development projects at Zealand Pharma. You will be part of the Biometrics Department, currently consisting of 2 statisticians, which is responsible for statistics, statistical programming and data management. We help create and implement clinical development strategies, manage standards, and provide expert sparring to external partners.
The successful candidate will:
- Develop and drive alignment of data standards and data collection processes
- Lead data management activities with clinical trial and submission teams
- Develop and implement new ideas, focusing on efficiency gains within and across projects
We are looking for a skilled and experienced Senior Data Manager for a permanent part-time position.
As a Data Manager, you will be expected 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’s Projects". You will be working in close collaboration with the Data Management team in order to manage the relevant data systems in the most efficient way.
You 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 (e.g. R, Perl, Python) is desirable. Furthermore, experience with eCRFs and data handling will also be valued positively.
Coloplast A/S, Humlebæk
Would you like to provide documentation to help us ensure product safety for our wound and chronic care globally?
As a test method specialist, you are responsible for validation and maintenance of test methods used in our productions. This means that you participate in creating documentation for test methods and related procedures and instructions.
Doing so, you will:
- Participate in the constant development of test method principles and structures in Global Operations
- Create and approve validation documentation for production-related test methods
- Partake in projects and in the ongoing maintenance of test methods implemented in our production
Jakob & Partners ApS, Copenhagen
Your job will be exciting and challenging and will demand a high degree of flexibility. You will become part of a highly qualified, truly international and top performing team. You will be working on a range of projects within different therapeutic areas and develop a unique insight of the pharmaceutical and biotechnological markets through internal training courses and interactions with internal and external experts.
Together with your colleagues you will be responsible for ensuring that scope and objectives are met throughout the entire duration of the project and that all requests are handled in a timely, accurate and relevant manner. The learning curve will be steep, but your “can do” attitude and the support you will receive from a focused dynamic team will push you to overcome the daily challenges. Your strong drive and sense of initiative will help accelerate your progression in Jakob & Partners.
Thermo Fisher Scientific, Allerod
Do you have a passion for sales and sales management? Do you thrive in a dynamic, international leading company, and are you looking for a role where you can assume the responsibility for optimization of business whilst applying your excellent people management skills to create results and lead a small group of dedicated team members, then you may be the one we are looking for.
Your responsibilities will include:
- Lead the Immunodiagnostics sales support team to meet identified goals
- Manage a small group of 5 dedicated team members
- Manage allocated application/demonstration/training requests ensuring timely and efficient, top class deliveries
O’Sullivan Consulting is recruiting for OFS in Somerset (USA), Avon (USA) or Brøndby (Denmark)
In the corporate New Business Development team, you will have a key role and be responsible for creating a MedTech pipeline of innovative applications for fiber optic technology to be used for analytical equipment, medical diagnostics, pharma and similar markets.
The New Business Development team in OFS is responsible for developing new business opportunities through mergers, acquisitions, partnerships, setting up new entities and the commercialization of new ideas from OFS Labs.
- Lead business development efforts in two new application areas for analytical equipment and diagnostics
- Identify and qualify potential business opportunities including prioritization and validation with data
Radiometer Medical ApS, Brønshøj
Do you have a passion for analyzing scientific publications, using your medical writing skills and do you like the thought of communicating cross-functionally in the HQ for a market leading Medical Device company? Then this might be your new career opportunity.
In Radiometer Medical you can use your experience in writing Clinical Evaluation Reports to ensure our mission of helping caregivers make diagnostic decisions that save lives.
You join our Clinical and Medical Affairs Team in an exciting period where we are expanding to meet the regulatory requirements for our broad and technologically diverse product portfolio. You can look forward to proactively lead the creation of Clinical Evidence Reports for the different product areas throughout the product lifecycle, and proactively communicate with relevant internal and external stakeholder on a global level.
Radiometer Medical ApS, Brønshøj
In the Regulatory Affairs Vigilance team, we collaborate with our colleagues to ensure that our products offer reliable, fast and easy patient diagnoses.
Our job is to communicate with health authorities on adverse events and other important events related to our products. This includes information on what caused the events and what the potential problem is, while ensuring timely notification of the authorities about our field actions worldwide.
We combine our ability of understanding health authorities’ legislation with structuring processes, creating efficient Standard Operating Procedures (SOPs) and asking the right questions to gather the information needed from our stakeholders throughout the organization.
We are seeking a highly motivated bioinformatician/computational biologist with excellent knowledge within human biology.
The main responsibility of the candidate will be to analyze serological biomarkers, genome-wide SNP data, questionnaires and electronic patient data from several Danish registries. Furthermore, a goal of the candidate is to develop risk-based models/algorithms by combining biostatistics and health informatics.
We are particularly interested in candidates who are enthusiastic about using multidisciplinary approaches in their work.The ideal candidate is expected to work independently with processing and analyzing data from the PERF cohort. You are expected to be comfortable with working in a dynamic and fast-changing environment and be able to communicate informatics results to scientists with biological backgrounds.
Y-mAbs Therapeutics A/S, Hørsholm
Y-mAbs is a listed biotech company based in Hoersholm and New York. We develop new treatment options for pediatric cancers. Y-mAbs Therapeutics A/S (Y-mAbs) is expanding and is now looking for an experienced Senior Medical Writer in a newly established position.
Are you our new Senior Medical Writer in a busy and ambitious working environment? This is your opportunity to join a dedicated team of professionals and become an important part of the Clinical Development staff of an innovative biopharmaceutical company.
- Build-up medical writing as a functional area
- Preparation and gate-keeping of regulatory clinical documents (e.g. Clinical Trial Protocols/Reports, Investigator’s Brochures, responses to authorities, Clinical Summaries and Overviews, DSUR)
- Planning and coordination of activities in a cross-functional setting
European Patent Office, The Hague/Munich
Are you an engineer or a scientist interested in joining an international team of highly qualified staff? Do you want to see the latest inventions?
We are currently seeking material scientists, with a master’s degree in engineering, physics, chemistry or natural sciences, to work as European Patent Examiners.
Your main responsibilities
- Carrying out patent examination from the search to the post-grant stage, and solving complex technical and legal problems in the process
- Taking a broad perspective to identify solutions whilst ensuring the uniform and effective application of the EPC (European Patent Convention) and other legal texts
- Creating and maintaining classification systems to ensure efficient and effective searching
Jobindex A/S recruiting on behalf of Medicologic A/S in Copenhagen
Would you like to be part of a team ensuring the highest levels of patient safety? You will be contributing to the development and approval of intelligent and innovative treatment methods within the medtech industry?
Medicologic is a leading Danish medtech consultancy and engineering company. Together with our customers we bring new and innovative products on the market with focus on speed to market.
With a strong pipeline of challenging projects we are seeking a passionate Senior QA/RA Consultant to join our QA/RA team in Copenhagen. Reporting to the Team Manager you will be part of our QA/RA team and interact with customers to solve hands-on QA/RA assignments.
You will support customers with relevant QA/RA activities from development of Quality Management Systems, Risk Management, Process Validation, audits at customer sites or 3rd Party Audits etc.
Thermo Fisher Scientific, Hvidovre/Skåne
We are currently seeking a skilled and dedicated Field Service Engineer to join our team of professionals and to further increase the level of our service; providing ‘above expectations’ customer service and satisfaction.
Reporting to the Service Manager, you will perform all service activities on Thermo Fisher Scientific’s own products within HPLC and LC-MS in line with internal rules and customer regulations assuring telephone support, diagnostics as well as on-site service.
- Ensure highest professional relationship with customer base to achieve customer loyalty and escalate issues if necessary to solve critical tasks in the fastest way possible
- Apply market knowledge, customer and technical insights to feedback to Manager for portfolio improvement and identify growth opportunities