Would you like a unique opportunity to take part in building a strong finance function in a valuable anti-viral Biotech company heading for an IPO? Synklino recently initiated development of the first drug candidate and are conducting pre-clinical studies and process development. You will be responsible for the finance function and the outsourced accounting. This, as well as and not least business controlling with your colleagues in the R&D and other functions. You will also be involved in investor relations and investor communication. It is also essential that you are able to support management in preparation of the annual reports and quarterly updates to Synklino investors.
The Challenge On behalf of Merck Life Science, Best Talent is now looking for an Account Manager Denmark– Process Solutions. The Account Manager is responsible for the sales revenues and the position focuses on continually sales growth through existing and new customers and supports the awareness of the portfolio throughout the field. Your focus will be on several Biopharmaceutical & Pharmaceutical manufacturing customers in Denmark. You will drive the business forward within this territory.
Do you also love clinical data, and would you like to lead all clinical study activities for super exciting surgical imaging systems to improve surgical outcomes? You will be joining a brand-new clinical function under development. As Head of Clinical Outcomes you will drive planning and execution of especially premarket Clinical Investigation in accordance with ISO 14155 but also PMCF clinical surveys, to generate the needed evidence.
Your focus will be on Biopharmaceutical & Pharmaceutical manufacturing customers in Sweden. You will drive the business forward, leading key strategic projects within this territory, coordinating customer support functions. You must have in-depth knowledge of the entire Pharma Processing product line, including Filters, Single Use, Cell Culture Media, Biological, Dry Powder & Liquid Buffers & GMP process chemicals used in customer’s Biological & Pharmaceutical production processes. This will allow you to provide tailored & experts advise to customers and help them meet their objectives.
If you like to put your statistical programming skills and mindset into actions and you are looking for a clearly not-average job as a Senior Statistical Programmer, you have it here. You will be part of a dynamic team of 4 highly motivated programmers and +15 external consultants in a stimulating international research environment, where high influence on the working processes can be gained.
If you excel within HR strategy and you are looking for a job with maximum impact and influence, this is what you want. You will head a team of 12 highly skilled and dedicated people in the HR organisation. You must lead the HR function in a cross functional way- meaning supporting local management and department heads on all HR related matters and issues by providing input, guidance, and coaching. The Senior Director is head of the HR department and an active member of the Leadership Team at Ferring IPC. You will be responsible for the development and execution of the local HR strategy in support of the overall business plan; strategic direction; succession plans; organizational and performance management as well as learning development, and payroll, compensation and benefits. You must provide leadership by articulating HR needs and plans to stakeholders and be a strategic partner to drive the Ferring People agenda for the site.
The successful candidate will lead DSM’s global scientific advocacy for Human Milk Oligosaccharides (HMO) for all life stages. Particular focus will be in the Early Life Nutrition (ELN) segment, which includes infants, young children, children, and maternal nutrition. You will develop scientific substantiation for the nutritional suitability and health benefits of HMOs and other DSM ingredients and solutions in order to support business and regulatory objectives. In collaboration with internal and external stakeholders you will also develop science-based value propositions related to HMOs, alone or in combination with other ingredients, and will help to advance them with global customers and into the regional markets.
As Project Manager you will be responsible for one or more projects, primarily focusing on spray drying plants and process engineering. Your responsibility will include all aspects of project execution from hand over from sale to the final takeover of the plant according to the GEA Project Management Plan. You will facilitate the installation and take the lead in the and qualification of the plant. As Project Manager you work in a complex field where the job requires dialogue with clients based on your technical know-how and interest in solving technical challenges and finding solutions for and together with the clients first phase as well as on site.
As a Process Specialist you will be part of a team responsible for process and plant design specifications of drying technologies where you support the sales team in quotation preparation and the project team throughout the project phase. As a Process Specialist you work in a complex field where both a technical know-how, analytical skills, and a commercial mindset are important factors and given in this role.
As Senior Design Control Engineer, you will be joining a team of medical device engineers and scientists working in the cross-field between device development, production transfer and technical support to the production site. The position requires extensive experience with development of medical devices with focus on design control and risk management. The position is an opportunity to contribute to the development and documentation aspects of the Life Saving Device, a drug device-combination-product. You are responsible for the risk management activities, as they move from project initiation through development and testing, manufacturing, global submission, and commercialization.
Your desire and ability to develop sales within a new technology is important. The system developed, produced and marketed by CelVivo has a great potential with the field of 3D cell culture. This new technology have shown unparallel resemblance with in vivo conditions. You will be given the opportunity to influence the development where you introduce this new technology to the market. The role is a key role with focus on direct sales, follow up and training of customers and distributions partners worldwide. The customers will be approached by you and followed up by competent Application Specialists in close collaboration.
As Senior Medical Device Scientist, you will work with Usability Engineering and Design Control. You will be joining a team of medical device engineers and scientists working in the cross-field between device development, production transfer and technical support to the production site. The position requires extensive experience with development of medical devices with focus on design control and usability.
Do you think strategically, and can you act operationally? Would you like a unique opportunity to take part in building a strong and valuable anti-viral Biotech company heading for an IPO?
You will act in a close collaboration with several external Contract Manufacturing Organizations (CMOs) and process SMEs internally at Ascendis Pharma. It is expected that you find solutions and that you can think out of the box within your area of responsibility. You go through different processes to drive the area most effectively for the team and the company. The team is characterized by high quality, result orientation and speedy realizations of the goals in an entrepreneurial environment.
Head of Biology Group Human Milk Oligosaccharides & Early Life Nutrition, Royal DSM/Glycom / 1751/CLOSED
As Head of Biology Group, you will be a key part of our diverse team in Hørsholm. You will lead the HMO Biology Group and be responsible for driving the strategy for research activities and innovation areas within Human Milk Oligosaccharides, for both infant and adult applications. You will work cross functionally and lead collaboration efforts with Innovation, Regulatory, Marketing, Commercial, IP stakeholders across DSM to deliver business and scientific projects and to ensure technical competence development.
The QC Carrier, Linker team is one of four teams in the Drug Substance Manufacturing (DSM) department. The team consist of 5 persons, which is expected to grow as more products are moved to the commercial part of the organization. The Challenge You will as QC specialist be responsible for keeping QC oversight of starting materials and intermediates produced and analysed at CMOs. You will be reporting to the Director, QC Linker Carrier and join a team of highly experienced and social colleagues working together to obtain the best results in a timely manner.
As a Project Manager you will be responsible for one or more projects primarily focusing on spray drying plants and process engineering. Your responsibility will include all aspects of project execution from contract negotiations to the final takeover of the plant according to the GEA Project Management plan. You will facilitate the installation and take the lead in the commissioning of the plant.
On behalf of Merck Life Science, Best Talent is now looking for a Senior Technical Application Consultant Upstream, Scandinavia. Leveraging your technical expertise from cell line generation to manufacturing of GMP cell culture media and supplements.
Medical Scientific Liaison Dermo aesthetic You enjoy facing the field by being a strong communicator of scientific topics at all levels State of the art products within medical devices and dermo aesthetic You create and develop new and strong partnerships Influence and development of own job content Challenge IBSA aims at developing market share by its state-of-the-art products in a combination with even stronger communication to the market. This calls for extending the organisation by engaging a highly skilled Medical Science Liaison (MSL) to cover the Nordics within the Dermo aesthetic area. The role is a field-based position co-responsible for the relationship with IBSA Nordic KOL Team and for the scientific information and the appropriate utilization of specific IBSA medical devices and products within the assigned therapeutic area. The MSL will support development of the Medical Sciences Plan by using a scientific approach aligned with the overall commercial strategy, therapeutic area objectives and an in-depth understanding of the vision. The MSL will need to be a credible and valued scientific resource in a variety of scientific interactions with key stakeholders across assigned regions. The primary role is to build and foster strong relationships with KOLs in the therapeutic area, support education and training of internal as well as external parties and to bridge scientific communication to stakeholders. You will report to the Nordic Managing Director and work in close cooperation with Sales & Marketing Manager.
Associate Director/Director of Safety Surveillance Making a real difference being at the forefront of biological cancer treatment You are ready to take on responsibility for leading safety surveillance Dedication needed for aiming at excellence The Challenge You will join Y-mAbs at an exciting time as they have already established a broad and advanced product pipeline, including one FDA approved product, DANYELZA® (naxitamab-gqgk), and one pivotal-stage product candidate, omburtamab, for which a BLAs and MAA have been submitted. As an Associate Director/Director of Safety Surveillance your responsibility will be to develop and successfully execute the safety surveillance strategy both within clinical trials and post- marketing for assigned products. You will apply your strong safety knowledge and skills in all aspects of surveillance, including signal detection and evaluation, authoring safety-related documents, and providing expert input into the safety monitoring and risk management strategies for clinical studies and programs.
Are you the one to join AFRY in their ambition to make a difference? Can you think strategically, create coherence cross the sectors and secure the continued favourable commercial development within the full line of business mentioned above in new and existing sales areas? The Business Unit, BU Øresund, is focused on delivering successful projects and professional consultancy assignments within the Life Science sector. Together with the Business Unit Manager you have the opportunity to drive the strategic sales across the organisation in the Life Science business with both existing and new customer relationships in the Öresund Region and also at international organisations with Headquarter & organisations in the region.
Lead the product design activity to ensure timely and accurate completion of tasks. To be a direct communication link between the lab, the plant, sales, and the customer to ensure appropriate product design, process uniformity and product quality.
We are in search of a skilled and experienced Senior Validation Analyst, who will support the IT team with compliance activities for the life-cycle management of infrastructure systems.
Syntese has as a global important API provider within Pharma GMP great potential, and you will be a valuable member of the Management Team in the development of the company. As the new Head of Engineering, you will be responsible for leading and developing your team and employees.
Büchi Labortechnik AG, the market leader within solutions for laboratory rotary evaporation, experiences great success also in the Nordics. A new role has therefore been created to be able to provide direct and outstanding service in Denmark and Sweden primarily covering the Øresund region.
Do you bring solid experience from working with GxP IT systems in the pharma business? Are you at the same time looking for an opportunity to bring all of your skills into play in a role where your knowledge and ideas are just as appreciated as expected? If so, you now have the chance to influence our future way of handling our new clinical trial management system, Veeva Vault – how we work with Vault Clinical and secure on-going optimisations. You can look forward to being part of an organisation that believes good ideas need room and nourishment to flourish.
On behalf of Merck Life Science, Best Talent is now looking for 2 Account Managers for sales of process GMP to big pharma. The 2 Account Managers will have separate client responsibility in a growing market. You will be working at the heart of the business with few big clients, where you are the primary point of contact for generating business within the segment Biopharmaceutical Manufacturing in Denmark.
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.
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.
Make a difference by Serving Pharma 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.
As a proactive Systems Sales Engineer, you will be working at the heart of the business. By creating leads and sales opportunities you will interact with prestigious companies and organizations in Denmark and in cooperation with the team, you create state-of-the-art solutions for our customers. At the same time, you will join a company where you can learn from the best engineers in the industry. You will be promoting and helping customers to monitor, control and protect new and existing clients with safety and process control systems and digital transformation software.
You will act in a close collaboration with several external Contract Manufacturing Organizations (CMOs) and process- and QC SMEs internally at Ascendis Pharma. It is expected that you find solutions and that you can think out of the box within your area of responsibility. You go through different processes to drive the area most effectively for the team and the company. The team is characterized by high quality, result orientation and speedy realizations of the goals in an entrepreneurial environment.
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.
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.
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.
Your desire and ability to develop sales within a new technology is important. Based on the culturing cells in 3D the system has great potential. Based on a technology where cell models grow with this new technology have shown unparallel resemblance with in vivo conditions. You will be given the opportunity to influence the development where you introduce this new technology to the market. The role therefore consists of more functions like direct sales, product demos, applications and training of customers and distribution partners in the Nordics.
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.
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.
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. You must also ensure, that efficient and transparent processes, systems and standards are in place and are used intelligently.
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.
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.
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).
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.
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.
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.
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.
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.
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.
On behalf of our client Ascendis Pharma, Best Talent is now looking for a Cross Functional CMC/Safety Toxicologist. You will be a central part in supportive toxicological/safety evaluation work of all Ascendis Pharma’s development projects.