You are an experienced Cell Culture Scientist who can provide engineering and scientific leadership to support clinical and/or commercial processes in the area of cell culture operations. In this position you will interact with cross functional departments to ensure a successful and smooth tech transfer of new products into their facility.
Som QA Projektleder får du en spændende og varieret hverdag i en virksomhed, hvor der er korte kommandoveje. Du bliver en del af de strategiske overvejelser, fordi det som QA Workstream Lead på SAP-projektet, bliver dit ansvar at sætte en compliant retning for implementeringen. Du får et udfordrende og selvstændigt job, hvor rollen giver dig en meget stor og tværgående kontaktflade til hele organisationen.
You will play a key role driving change initiatives while also leading the change of the business improvement program. The role offers great opportunities to contribute with process improvements, cost savings and driving a cultural change for the better of the company. The role will provide huge opportunities to evolve the business and for developing your own skills. As the head of Finance, IT and Procurement you will be responsible for a small team of 4 colleagues, consisting of a Controller, a Direct Procurement Manager and 2 people in IT. You will also work closely with our outsourcing partner for all accounting activities. You will need to combine financial knowledge with strong business acumen and strong change management mindset. You will likely have about 10 years of financial experience with product costing in a manufacturing site which is very important. It could be from a GMP regulated industry. You support HQ/Corporate Finance in the implementation of corporate finance programs, processes and procedures which are to be locally applied. Your goal should be to help the company achieve its strategy and targets by delivering on commitments for the change program and helping the company deliver on an ambitious growth strategy.
In this challenging position you will have the opportunity to take part in activities which potentially can change or save the life of patients. You will participate in the investment proces in one of the most exciting and profitable industries. You will continue to learn about human biology and talk to leading medical experts and doctors from all over the world. You will meet and work with highly talented and courageous entrepreneurs who manage to fund and develop new companies. Your week will consist of many different tasks and you will be involved in analyzing and forming opinions about the newest therapies, modalities and intrepetration of pathologies. You work with and support the investment team to analyze and present the investment opportunities, helping to ensure a process that leads to optimal investments.
As a central and specialty laboratory (GLP & GCP / GCLP) Unilabs provides a variety of services for the pharmaceutical industry, Biotech’s, CROs and the Danish Health Care. As a Project Manager for the Serving Pharma unit you are responsible, in cooperation with customers, for the set-up, procedure and method transfer, validations, clinical studies and commercial projects, e.g. Companion Diagnostics, across the CoE. Unilabs wants to strengthen their growth by working towards a PMO organization. In achieving this goal, your knowledge and personality will be a very important contributor and you will have a lot of responsibility and influence on implementing new best practices and tools for project management.
Experienced Manufacturing Scientist who can provide engineering and scientific leadership to support clinical and/or commercial processes in the area of protein purification operations. The Purification Team is part of the Process Sciences department which provide scientific leadership to support clinical and commercial processes. Process Sciences operate in areas of cell culture and protein purification operations, and act as lead on technology transfer teams and investigation teams. The department continuously strives to identify opportunities to improve systems and practices and provide direction to the manufacturing group as well as technical development teams.
The Program Manager (PM) is accountable for the planning & delivery of programs from the point of contract signature (Scope of Work / Letter of Intent / Contract) through program closure. The PM ensures that the provided services are in alignment with their contracted commitment to clients and the company vision/mission/strategy. As PM your responsibility will also be to develop and successfully execute the contracts according to development/ manufacturing schedules for assigned products. You will achieve this through close collaboration with your other colleagues in the department as well as Stakeholders in other functions. You will drive tasks and projects forward in an active and leading role. The PM typically handles an average load of 4-6 programs and receives coaching, guidance & support from peers and the Head of Program Management.
The Business Development Manager Nordic is responsible for a profitable business in the assigned territory through direct sales, with key focus on ELISA sales and system placements whilst managing additional business partners (agents). This position focuses on continually sales growth through existing and new customers and supports the IDS awareness throughout the field.
Your main responsibility will be to lead the bioanalytical team, providing services for pharma, CRO and biotech clients. You will be responsible for a team of 16 employees and involved in the strategy and business plans for Wieslab. You will lead, advice, coach and develop your team, and support them in their role. You will ensure ambitious goals and solutions and follow-up on activities and resources. This includes participation in setting, communicating and following up on goals for the department as well as ensuring continuous development in tools and processes ensuring timely delivery of quality data to clients. You work in close collaboration with the other managers and colleagues across the Svar organization. You will use your scientific knowledge and experience to influence the project decisions across the entire area.
If you bring a strong background in Cellular Immunology, and if you are looking for a job with major impact, influence and development opportunities, you may be the candidate we are looking for. In Ferring Pharmaceuticals, there is a a long history within the treatment of inflammatory bowel diseases, and a wish to expand their efforts in order to help more patients worldwide.
Viminco producerer primært tabletter til både generiske og originalprodukter. Tabletterne kan filmcoates eller drageres. På flere kritiske ressourcer har de identisk udstyr, som kan øge fleksibiliteten og robustheden i gennemløbet. Med en produktion på 600 batch om året og mere end 50 forskellige produkter, er deres produktportefølje bred, hvilket giver en effektiv og fleksibel produktionsafvikling. Som Process Specialist bliver du en del af produktionen, som består af 18 operatører og 4 personer på supportkontoret. Dit ansvar bliver at bidrage til at højne standard og gerne løfte den yderligere således, at Viminco kan leve op til deres mål om at levere produkter af den bedste kvalitet. Som Akademiker i produktionen, har du en nøgleposition, hvor du bidrager med din viden inden for GMP og virkelig kan gøre en forskel i form af at finde nye løsninger og ”tænke ud af boksen” ved forskellige problemstillinger
Som Teknisk Chef bliver du en del af et dynamisk team, som består af 4 dygtige ingeniører og håndværkere – et team, der også fungerer som sparringspartner for koncernens PT-gruppe, hvor alle arbejder mod fælles mål. Du vil blive en del af teamet med selvstændigt ansvar og stor mulighed for at gøre din faglighed gældende i projekter og primært i det daglige vedligehold og trouble-shooting. Jobbet er alsidigt; fra design, montage og kvalificering til vedligehold af maskinpark og bygninger. Da BIOFAC er en mindre virksomhed, vil en hel naturlig del af arbejdet derfor være både udførende og koordinerende og med ansvar for gruppen.
Med reference til virksomhedens CEO, får du ansvaret for produktionen, som er opdelt i 3 forskellige afdelinger for henholdsvis skærm-, antispray- og klokkeproduktion. I rollen bliver du en vigtig del af virksomhedens ledergruppe. HBN-Teknik A/S producerer 24/7 med 3-holdsskift alle hverdage og weekendskift i en del af produktionen. Du indtager en nøglerolle og bliver et vigtigt omdrejningspunkt for den plasttekniske produktion og produktionsudvikling, ligesom en vigtig del af dit ansvarsområde bliver at sikre fortsat udvikling og forankring af viden og kompetencer i virksomheden.
You will join Y-mAbs at an exciting time as they have already established a broad and advanced product pipeline, including two pivotal-stage product candidates, for which the company’s first BLAs have been submitted. As Associate Director/Director your responsibility will be to develop and successfully execute the safety surveillance strategy for assigned products.
Viminco develops and produces products together with Orifarm, combining Orifarm’s commercial and regulatory know-how with Viminco’s knowledge about pharmaceutical formulation development, analysis and production, starting materials and current legislation to obtain a significant competitive advantage. As Development Project Manager, you will be responsible for managing the scientific and technical work including development project meetings and detailed timeline for the development phase.
Dit primære ansvarsområde bliver den kontinuerlige påvirkning af organisationen med henblik på oparbejdelsen af en reel leankultur og adfærd, hvor alle medarbejdere har et naturligt fokus på helhedsløsninger og løbende optimeringer. Vores strategi for lean er endnu ikke på plads, men flere leanaktiviteter er igangsat. Din rolle bliver at udvikle en strategi og omsætte denne strategi til praksis. Strategien skal have rødder i Ferring TechOps’ leanstrategi, der tilpasses Synteses behov.
QC- afdelingen er ansvarlig for at analysere råvarer, mellemprodukter og færdigvarer. Laboratoriet udfører en lang række kemiske analyser, fortrinsvis efter diverse pharmakopéer, og er udstyret med bl.a. HPLC, GC, ICP, UV, IR, m.m. Data rapporteres i LIMS. Afdelingen består i dag af 2 kemikere, 9 laboranter og en Laboratorieassistent. Hovedopgaven er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne. Du vil blive involveret i udvikling og validering af metoder samt implementering og kvalificering af analyseudstyr. Du arbejder med daglig trouble-shooting i forbindelse med afvigelse- og OOS-undersøgelser samt ændringssager iht. GMP-krav og deres kvalitetssystemer.
You will be part of Commercial Operation and responsible for creating, implementing and manage the near and long-term marketing strategy of your designated product portfolio. You will work primarily with the Svar Complement System and ELISA product areas, focusing on improving customer satisfaction, keeping the products aligned with the organization’s broader strategy and driving business growth.
For alle projekter gælder, at du er medansvarlig og ansvarlig i alle projektfaserne, og det vil være dig, der efterfølgende er den tekniske support ved tunge problemstillinger. Det er også dig, der præsenterer ved diverse GMP audits, ligesom du også bliver ansvarlig for budget-input i forbindelse med de kommende års projekter i forbindelse med udvidelserne på sitet.
I det pågældende projekt, kommer du til at referere til projektdirektøren i en matrixorganisation. Du vil få et større ansvar for flere forskellige udstyrsunderprojekter. Du bliver overordnet ansvarlig for fremdrift, økonomi og kvalitet. Rollen betyder, at du har flere interne SME´ere til at arbejde for dig og sammen med dig i projekterne. Du bliver en del af projektet, således, at der bliver en naturlig og tæt interaktion mellem dig, projektdirektøren samt de øvrige projektdeltagere, herunder de tilknyttede eksterne konsulenter.
I forbindelse med et større projekt, har Bavarian Nordic brug for nye GMP-vaskemaskiner, GMP- Kill-autoklaver og CIP/SIP anlæg. Du vil blive Projektleder og teknisk specialist på disse typer udstyr, hvor du sikrer fremdrift, kvalitet, inddragelse og kommunikation til projektorganisationen samt øvrige interessenter omkring projektet. Du vil blive støttet af projektet og tilhørende konsulent ressourcer.
These tasks require the ability to see the bigger picture and strategically build a strong network with decision makers at different levels of the hospital chain as well as understanding how the customer operates to be able to understand how J&J can bring more value. The SAM role will work across the Sales, Marketing and Value Creating organization to support the other Account Managers and this role will take lead in the tender shaping with focus on evaluation of value and on including new services and solutions. You will be given the opportunity to influence the strategy and maximize profitability in line with the company’s visions and values. You execute plans and strategies to accelerate growth and increase the company’s value offering. The SAM will be part of the Commercial leadership team for Denmark and report to the Danish Country Lead.
Your main responsibility will be to lead the R&D area and drive or participate in investigations and development projects. Svar Life Science is providing products and services to pharmaceutical, CRO companies, clinical hospital laboratories and providers of diagnostic automated systems.
If your field of expertise is in mucosal immunology and you are looking for an opportunity to make an impact beyond the average, we have just the right job waiting for you. As part of a newly established discovery team you will play a key role in expanding Ferring’s long history of treatment of inflammatory bowel diseases (IBD).
Your experience and ability to execute will be crucial for the development and growth of this position. You will be part of the Global Sales and Marketing Department and will be involved in maintaining and developing Global Sales Activities. You will be given the opportunity to influence the further development of a successful Danish company that helps the life science sector optimize their use of biomedical data in research and development projects to develop tomorrow's medicines better, faster, and cheaper. Intomics provides customized analyses and solutions that satisfy the needs of each individual customer project and can be relevant in various stages of drug research, such as biomarker discovery and optimization, target identification, drug discovery, patient stratification and translational research. The products also include new unique Data Analysis Tools, Infrastructure elements and Service Projects.
As Global Sales and Marketing Specialist you will have an important role in supporting the commercial activities of Intomics. Your work will be split between your own personal projects and support for your colleagues in the S&M department. As with all other roles at Intomics, you will work with a high level of freedom to influence the work that you do. At Intomics we focus a lot on working as teams to strengthen the outcome of what we do, and it is important that you get energized from working with others. You will be involved in a range of different projects and have many activities going on at the same time. Therefore, it is important that you know how to plan and prioritize your time to meet agreed deadlines.
The job of the Director of Product Technology is to continue defining Aligned Bio’s nanowire-based products while leading the strategy for the implementation of those products. In addition to product definition, the role includes working with the regional sales directors to target and support key customers, determine the appropriate technical marketing strategy and presenting at technical conferences. The Director of Product Technology will manage Aligned Bio’s Immunoassay Development Scientist as it relates to both the company’s internal development work and joint development work with customers. Eventually, the Director of Product Technology will be tasked with managing the Biomarker’s product P&L.
The job of the Senior Immunoassay Scientist will be to drive the further development and optimization of Aligned Bio’s nanowire-based products at the scientific and technical level. The Scientist will also assist in developing the strategy for the implementation of those products in the market. In addition, the Immunoassay Scientist will work with customers to integrate and optimize Aligned Bio nanowire platforms with the customers’ existing applications.
You can expect to be working according to highest standards of current practice in order to fulfill the company’s needs for data acceptable worldwide. Reporting to the Associate Director for Medical Devices, you will be the new Global Regulatory Affairs project team member providing regulatory Medical Device expertise and strategy. You ensure the required Medical Device certification and project support enabling global submissions and approval of medicinal products. You will work closely with the Global RA Product Manager in the Global Regulatory Project Team and the subsequent Medical Device and drug product teams.
The Business Unit has great growth potential, and you have the opportunity to become the next valuable member of the Management Team. As the new Business Unit Manager, you will lead the development of the Life Science business with both existing and new customer relationships in the Öresund Region. Furthermore, you will be responsible for leading and developing your team and employees.