24 job matcher din søgning
Chr. Hansen A/S, Hørsholm
To our department Portfolio and Project Management in Hoersholm we are looking for an Innovation Project Manager to drive high impact new product development projects.
You will lead innovation projects, which have a high commercial potential and strategic value to Chr. Hansen. Through close collaboration across commercial development and innovation you deliver new product development projects and programs on time, within resource & cost allocations, and to specifications.
As such, your main tasks will be:
- Plan and manage the project flow, end-to-end including target product profile and business case creation, project execution and post mortem analysis
- Secure timely execution of milestones, deliverables, quality, and budget targets and flag issues related to resources and/or competencies
- Manage project risks and proactively develop plans and recommendations to overcome delays or address drift from the original project plan
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.
Coloplast A/S, Humlebæk
You will become an expert on one of our product groups, e.g. Ostomy Care, Continence Care or Wound Care. You will be involved in change projects where you use your regulatory knowledge to evaluate and communicate the impact of changes to product components.
You will be working on multiple projects in close collaboration with specialists in marketing, clinical operations, supply chain and R&D, as well as our subsidiaries. To do so, you need to be comfortable communicating, coordinating and collaborating across functions and cultures, applying your proactive mind-set to plan, execute and meet deadlines.
- Participate in cross-functional projects for product modifications to ensure regulatory compliance
- Prepare regulatory files, clarify procedures and create or approve relevant documentation
- Communicate regulatory requirements across Coloplast
Coloplast A/S, Humlebæk
The Usability Specialist will be responsible for planning and executing the usability engineering process in new product development for medical devices. This individual will work closely with research and development, product management and regulatory teams to ensure that the usability of our medical devices properly address patient safety and needs, product performance, regulatory requirements and commercial needs. The usability specialist is the main responsible for late formative and summative tests/evaluations, and documentation in compliance with regulatory standards.
The function will also support user researchers in early formative activities for e.g. informing product usability requirements, identifying usability risks, creating task workflows and user interface concepts, and improving overall user experience.
Chr. Hansen A/S, Hørsholm
We are looking for a Manager for our Strain Development Department, in the Bacterial Physiology unit, Discovery function of R&D Chr. Hansen A/S in our headquarters in Hørsholm, Denmark.
As head of the Strain Development department your main task will be to manage a team of scientists and technicians, and to drive our research efforts within strain development and molecular tool development.
Other tasks include:
- You will set scientific direction in your areas of responsibility
- You will be involved in internal & external research projects aiming at developing methods for natural improvement of microbial strains and developing molecular tools for industrial organisms
- You will mediate internal and external collaborations
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.
Genmab A/S, CopenhagenGenmab is an international biotechnology company specializing in the invention and development of differentiated human antibody therapeutics for the treatment of cancer and other important human diseases.
The Project Assistant, CMC, will be a very important role in our CMC department. In this newly established position your key responsibilities will be:
- Work closely with and support the CMC Project Managers for projects
- Create agendas, minutes and capture outcomes of internal and external meetings
- Plan and structure meeting calendars between CMC Project Managers and external parties
Genmab employees work with determination and with respect for each other, consistent with our core values, to achieve our common goals. We give individuals and teams the autonomy to drive development of innovative products and solutions, knowing that integrity is a core value throughout our company.
LEO Pharma, Ballerup
Would you like to play a key role in the development of our growing portfolio - and are you an experienced Biostatistician, - then the opportunity is here.
We are in GCO Projects, LEO Pharma looking for an experienced biostatistician for a Biostatistics Lead role. GCO Projects is part of Global Clinical Operations, Research & Development. All Biometrics functions is in LEO part of Global Clinical Operations. The responsibility of a Biostatistics Lead is to contribute to the strategic planning of our development projects, and to ensure planning and execution of development activities in collaboration with relevant colleagues in Research & Development. As a Biostatistics Lead you are an important link between LEOs project organisation and the departments in Research & Development.
Are you motivated by achieving results together with a cross-functional team and driving a clinical development project through regulatory approval; are you passionate about solving statistical challenges in a company striving for global leadership within psychiatry and neurology by improving the lives of patients; then you are the right person for our vacant position as Project Statistician in the Biostatistics section at H. Lundbeck A/S in Copenhagen.
You will be the Project Statistician for a clinical development project working together with the cross-functional clinical project team. Project Statistician responsibilities include ensuring optimal designs and statistical strategies for the clinical studies and the clinical development plan in collaboration with other Lundbeck functions.
LEO Pharma, Ballerup
Can you set the direction and lead a team of highly competent specialists?
If you bring a strong combination of RA and R&D understanding backed by leadership skills, you have just the perfect foundation for this exciting job. That is, if you are motivated by the opportunity for influence on defining the way forward for LEO Pharma’s increasingly business critical way of working with labelling / product information to authorities, health care professionals and patients. You will put your personal mark on our way towards fulfilling our goal of becoming the world’s preferred dermatology care partner.
Your primary tasks will be to:
- Coach, guide and motivate your team of experienced specialists towards the defined goals
- Develop strategies and plans in dialogue with the team and RA Labelling Management Team
As a Sales Manager, you are responsible for supporting and developing your own geographical sales area in close cooperation with the local Tetra Pak market company.
You will work closely with our customers, your colleagues in the market companies, the support functions in the sales team, and your colleagues in other teams.
- Driving sales and actively developing the long-term relations to customers and market companies
- Listening to, understanding and analysing customer needs
- Planning and running customer seminars, trainings, and presentations
Xellia Pharmaceuticals ApS, Copenhagen
In this newly established team, you get a chance to apply your experience and knowledge to help set the bar for our serialization process – and shape your own role in an international organization with unique products and ongoing, exciting transition from being a B2B player into a fully-fledged B2i (business to Institutions) pharma company.
In the role as Serialization coordinator, you will coordinate and manage procedures guaranteeing that our products live up to both local and global requirements for pharmaceutical serialization. Doing so, you will help ensuring that the products can be tracked and traced through the entire supply chain – from manufacturing to delivery to our customers. You will be part of our Global Supply Chain (GSC) Systems and Master Data team in Copenhagen, Denmark.
Mercuri Urval søger for Braun Scandinavia
Ansvar for den innovative FUJIFILM endoskopiportefølje
En spændende stilling med rig mulighed for selvstændigt at drive og videreudvikle Braun Scandinavias endoskopiportefølje i tæt samarbejde med FUJIFILM. Klar kommerciel nerve i rollen med vide muligheder for produktejerskab, medindflydelse hos ledelsen samt påvirkning af agendaen i en smidig, professionel og moderne organisation, der agerer på et komplekst og kompetitivt marked.
I denne nyoprettede funktion som KAM refererer du direkte til Sales Director hos Braun Scandinavia og får selvstændigt landsdækkende produktansvar for Braun Scandinavias endoskopiportefølje fra FUJIFILM, der i mange henseender er selve kernen i Braun Scandinavias forretning.
Fertin Pharma, Vejle
As part of an ambitious growth strategy, we are looking for a commercially strong and structured Business Development Manager (BDM) with excellent communication skills.
The BDM will support creating and executing the strategy and product pipeline within Nicotine Replacement Therapy (NRT) products. Including taking lead on a number of opportunities and projects within same. To succeed in this role, the BDM must work with all aspects of the business development process from identifying, evaluating, recommending, and negotiating to implementation.
- Based on close collaboration with e.g. Marketing and R&D identify opportunities for concepts and products for development, out-license and supply
- Identify, prioritize and build relationships with potential new business partners
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, and are you looking for an opportunity to be part of one of LEO Pharma’s strategic established portfolios, this could be the position for you! You will get the chance to personally impact the regulatory strategies and deliverables and by this positively influence the goal of treating thrombotic patients.
As Senior Regulatory Project Manager in our Regulatory Affairs Focus Team, you will chair the cross-departmental RA focus team 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 the regulatory life-cycle strategies.
Compass Human Resources Group A/S recruiting on behalf of Sanofi Genzyme in Hørsholm
Being a global healthcare leader requires hiring the top talent in the market and Sanofi Genzyme is therefore searching for a new Medical Advisor, Oncology to add value and join the Nordic Baltic (NOBA) Medical Department. You will be based in Denmark while collaborating with your colleagues across the NOBA region.
As a Medical Advisor, you will be a medical expert in the therapeutic area of oncology. Your finest task is to drive and execute medical and scientific communication and activities in collaboration with external stakeholders and in line with the Sanofi Genzyme business strategy for the oncology therapeutic area.
The key to success in this role is to develop and maintain relationships with regional and national Key Opinion Leaders (KOLs) to strengthen their product knowledge and build an advocacy base among external specialists within the oncology area.
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
Join a Fast Growing Biotech Company, entering a new phase
Ascendis Pharma A/S, a visionary and ambitious company, offers you a once-in-a-lifetime opportunity to become a major participant in the further establishment of the structure and function of Commercial Manufacturing.
As Vice President Commercial Manufacturing at Ascendis Pharma you will have responsibility over Commercial Manufacturing/Technical Operations.
Your main tasks are:
- Overall responsibility for CMOs and all technical operations
- Overall responsibility for providing leadership and oversight for the ComMan area in Ascendis
- Provide input to the strategic development of PS as part of the company’s PS Management Team
- Support Proccess Verification/Qualification (PPQ) including parameter studies
- Support filing, launch and preparation for regulatory inspections.
Coloplast A/S, Espergærde
As a QA specialist, you help create groundbreaking medico products that help people with intimate healthcare needs. Working on projects from the initial design phase through to manufacturing, you get to oversee every step of the way, collaborating with a large network of stakeholders and ensuring that our QA project delivery processes are aligned.
As part of the Quality department, you will be based in Mørdrup, 40 kilometres north of Copenhagen. Working alongside 20 colleagues in Quality, you will be one of the 5 QA specialists responsible for the development of new products in our Pilot production.
Your role involves a high degree of cross-organizational collaboration and you can expect up to 20 days of international travel per year. In addition to working closely with your colleagues in the project teams, you will have a close link to other R&D functions, as well as the Global Quality organization in Head Quarters.
Novozymes A/S, Bagsværd
At Novozymes, we work in close partnership with our customers and the global community to make a sustainable impact. We use science to advance industries, and as part of Research, Innovation and Supply, you will produce and deliver the biological solutions that boost our customers’ business and pave the way for a brighter future.
We are looking for an energetic, motivated and action oriented person to enter a newly established role as Supply & CMO Manager in the Human Health Operations function.
You will be working within a cross-functional team within Novozymes Incubations & Acquisitions area, responsible for supporting new business areas for Novozymes. We are a dedicated and versatile international team consisting of business developers, scientists and operations people with a strong drive to realise the value of new growth platforms created on Novozymes science and technology.