77 hittade annonser
You will play a key role in the experimental work of setting up advanced immunoassays (ELISA, MSD, AlphaLISA) to quantify biomarkers in relevant biological matrices, as well as characterization of antibody-antigen interactions to guide lead selection and engineering activities in antibody discovery campaigns. Your work will also include development of cell based assays and biosensor-based characterization of antibody-antigen interactions such as measurement of affinities and epitope binning. The majority of the work will be done in close collaborations with a single academic in the Biologics team.
We offer the opportunity to join an innovative team of highly qualified colleagues working in a scientific environment dedicated to discovery of antibody based drugs for treatment of neurological diseases. We work in an open and collaborative atmosphere with excellent possibilities to develop technical skills and scientific expertise.
Jakob & Partners ApS, Copenhagen
Pharmaceutical sciences, biotechnology, medical devices
If you want to work for a highly successful company providing research and analyses of markets within the pharmaceutical and biotechnological industries, you should consider this position in Jakob & Partners. You will be part of a highly qualified team with expertise within life and pharmaceutical sciences, market insights and economics.
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 training courses and interactions with internal and external experts.
SPX Flow Technology Danmark A/S, Søborg
Are you a skilled Technical Sales Manager, who can build strong relations with customers, stakeholders and colleagues? Would you like to take on a key position in an international market leading organisation, where you get to travel the globe?
We are a global supplier of highly specialized, engineered solutions with operations in over 35 countries and sales in more than 150 countries globally. Our innovative solutions play a critical role in helping meet the rising global demands in the end markets we serve.
You will be responsible for:
- Collaborating closely with the Engineering, Project Management and Supply Chain functions to ensure process definition, prices and quality.
- Developing a working knowledge of the markets and customers’ processes, organizations and overall business to gain a competitive selling advantage for the company.
Unique Human Capital recruiting on behalf of Zealand Pharma in Glostrup
Work with QA in a fast growing and exciting biotech company
As QA Manager – CMC at Zealand Pharma you will become a part of the QA organization overseeing all activities and delivering professional quidance to ensure GxP compliance within all areas. You will be responsible for the overall QA oversight for one of the current phase 3 products applying your knowledge within GMP. The department is headed by the Vice President, Head of QA, and in addition to this position, encompasses 7 QA colleagues. You will be reporting directly to the Vice President, Head of QA.
Your key responsibilities
- Employ GxP QA expertise during the development providing GMP compliance guidance to internal stakeholders
- Influence the compliance of projects and programmes
- Review and approve internal and external documentation
Nomeco A/S, København
I Nomecos SygehusService søger vi en ny serviceminded kundekonsulent til vores team. Opgaven er enkel – at yde den bedst mulige service til vores kunder.
Som kundeservicekonsulent i SygehusService er du Nomecos ansigt udadtil. Du vil dagen igennem være i kontakt – både telefonisk og via e-mail - med sygehusapotekerne, som du med en positiv og åben indstilling skal servicere og vejlede.
Det er et job med et stort ansvar og en høj grad af selvstyring. Vi koordinerer løbende vores opgaver med Nomecos fire filialer samt indkøbsafdelingen, lager og kørselsafdelingen, og du får derfor også en stor kontaktflade både internt og eksternt i Nomeco. Daglige tavlemøder, tæt sparring og one-to-one samtaler hver 6. uge hjælper os med at holde snuden i sporet – og det hele foregår i et afslappet miljø og en positiv omgangstone.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
High degree of influence in an exciting and fast growing biotech company
The Process Manager will work closely with the Global Clinical Development team leading/supporting the process changes, updates and compliance, and R&D operation's strategic directives. You will do that by ensuring the development and management of processes that enable compliance and standards across departments and apply best in class methodologies.
You will also drive global process improvements projects and support ongoing evaluation. You will lead the creation and maintenance of our processes – including but not limited to SOPs, guidelines, written instructions and other documentation processes. You will also ensure adherence to applicable guidelines/regulations.
As Process Manager, you will be responsible for effective implementation and creation of training sessions.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within drug development - and are you passionate about the voice of patients and their caregivers?
Lundbeck’s focus is first and foremost on the patients suffering from Alzheimer’s Disease, Parkinson’s Disease, depression and schizophrenia, for whom we develop innovative medical treatments. In the Medical & Regulatory Science business unit, we strive to integrate patient perspectives in our activities.
Your job will be at the center of this, helping us to develop and operationalize patient and caregiver insights linked to the regulatory and medical aspects of our drug development strategies. We would therefore expect you to have a passion for patient focused drug development combined with the skills and educational background to understand and navigate medical and scientific data.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Nonclinical Safety Research in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges across the company. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
We are searching for a graduate, with an interest in nonclinical activities, to support our development projects and marketed products. Your “home base” will be in Department of Bioanalysis, but you will work closely with other departments inside and outside Nonclinical Safety Research.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Clinical Pharmacology in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges cross functionally. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
We are searching for a graduate who can support Quantitative Pharmacology in the daily work and help us in our mission to become a world class pharmacometric service provider for Lundbeck.
Symphogen A/S, Ballerup
The position as (Senior) Drug Product Scientist offers a unique possibility to take part in the de-velopment of Symphogens antibody products. You will mainly be responsible for drug product process development and manufacture from early stage IMP manufacturing and later stage manufacturing including process validation strategy.
You will collaborate closely with staff from our CMC group and in project teams, to ensure de-velopment progress of Symphogen’s antibody lead candidates.
Tasks and Responsibilities:
- Tech transfer of manufacturing processes to CMOs
- Technical responsible for drug product manufacturing documentation
- Ensure implementation of drug product manufacturing strategy between projects
Ferring Pharmaceuticals A/S, København
Would you like to join us in a challenging position as Clinical Trial Manager (CTM)?
Clinical Operations is responsible for planning and execution of clinical trials in phases 1 to 4 within all therapeutic areas in Ferring Pharmaceuticals. High quality trial data and adherence to timelines are important for us. To optimize the achievement of this, a good and constructive teamwork and strong leadership abilities in accordance with our values, are critical success factors.
Are you ready to manage Clinical Trials in an international environment? We are looking for a Clinical Trial Manager to effectively plan and oversee the assigned clinical trials as part of international trial teams. As part of the Global Clinical Operations team, you will work in an international environment with approx. 50 dedicated and highly skilled colleagues.
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?
As Senior Regulatory Project Manager in our Regulatory Affairs Focus Team you will chair cross-departmental RA focus team(s) 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 regulatory strategies.
Your key responsibilities will be to:
- Lead the regulatory focus team(s) for one of LEO Pharma’s strategic established products
- Prepare Global Regulatory Strategies and ensuring implementation hereof
- Ensure business perspective across functions and high regulatory quality
Experis søger for Paranova i Herlev
Paranova, parallelimportør af medicin, søger en kvalitetsbevidst Commercial Lead til at udvide og vedligeholde samarbejdet med kunderne i Sverige, hvor produktporteføljen består af receptpligtig medicin.
Du starter i et barselsvikariat, da vores nuværende Commercial Lead går på barsel i juni og efterfølgende bliver du ansat i en lignende stilling på et andet relevant marked, da vi er en virksomhed i vækst.
I rollen som Commercial Lead er du ansvarlig for at drive Paranovas salg af receptpligtig medicin til apotekskæderne i Sverige. Dette indebærer:
- Håndtering af tilbud
- Forhandling af aftaler og rabatter
- Identificering af nye produkter til det svenske marked (i samarbejde med Research Team)
Zealand Pharma A/S, Glostrup
Zealand Pharma A/S (Zealand) is looking for an experienced patent attorney to join the IP Department, which presently counts two patent attorneys and one assistant. Key responsibilities will include building up IP strategies, patent application drafting, filing and prosecution together with patent search and analysis.
Zealand has built a large and diversified patent portfolio, and considers protection of inventions in peptide drug discovery and development to be key to our business success.
We offer a combined salary package including pension scheme and health insurance, as well as the option of joining the company lunch program, and use of massage, fitness and social facilities.
Manpower søger for Agilent i Glostrup
Manpower søger på vegne af Agilent en laboratorie opvasker, med start hurtigst muligt, til laboratorie opvask i medicinalindustrien i Glostrup.
Arbejdet består af betjening af halv- og fuldautomatiske industriopvaskemaskiner, indsamling af opvask og levering af rengjort opvask. Du får en stor kontaktflade blandt laboratorie- og produktionspersonalet. Det er din vigtigste opgave, at leve op til de høje hygiejne- og kontrolkrav, der er forbundet med opvask af laboratorieudstyr.
Grundig og kvalitetsbevidst
- Du har muligvis erfaring med laboratorie opvask fra enten medicinalbranchen eller et hospital og har et godt praktisk håndelag
- Kendskab til GMP/GDP/GLP er en fordel
- Du skal kunne dansk i skrift og tale og have brugerkendskab til PC-arbejde
LEO Pharma, Ballerup.
Do you have a strong quality mind-set? Do you have interest in and experience with Packaging Materials within the pharmaceutical industry? Do you have experience with cooperation with 3rd parties? Then you may be the Senior Quality Professional we are looking for in Patient Supply and Suppliers Quality.
The PSSQ department is a global department at LEO Pharma, responsible for handling of all GPS suppliers of API’s, packaging materials, raw materials, and excipients. Furthermore, the department is responsible for supporting Distribution Management, including 3PLs and freight forwarders, and Customer Order Management.
As our new Senior Quality Professional your primary responsibilities will be:
- Planning, performing and follow up on audits of all primary and secondary packaging materials
- Establish and maintain Quality Agreements (primary and secondary packaging materials)
Radiometer Medical ApS, Brønshøj
Do you want to take commercial lead for our innovative sampler product portfolio and contribute to Radiometer’s Global Market Leader position in Critical Care Diagnostics?
In this job, you truly pull the strings when it comes to managing the product. You will be the global go-to-person for the sampler area with great global visibility in our organization working closely with the Global Marketing Team, Sales, Finance, Clinical & Medical Affairs, R&D, Supply Chain, RA/QA and our marketing and sales colleagues in our subsidiaries.
We offer an exciting position in a dynamic global business environment, with a unique opportunity to demonstrate results at all levels in the Radiometer organization and thereby further grow your career in Radiometer.
Jobindex A/S søger for A-Consult Group A/S i Søborg
Sæt din ekspertise i spil i en udadvendt rolle, hvor du hjælper pharma- og medicovirksomheder med at overholde lovgivningen inden for pharmacovigilance.
Du indgår i vores team af 3 erfarne konsulenter, som rådgiver vores kunder inden for alle aspekter af pharmacovigilance. Vi fungerer som kundens sparringspartner, og opgaverne kan indeholde alt fra mindre litteratursøgninger til samlede rapporter og omfattende sikkerhedsvurderinger.
Konkret betyder det, at du:
- I samarbejde med kunden afdækker og beskriver deres behov for at finde den bedste løsning
- Laver litteratursøgninger for at afdække, om der er beskrevet bivirkninger, og du laver benefit/risk-vurderinger mht. evidens og risici
- Udarbejder aggregate reports eksempelvis PSURs og DSURs
Hays Specialist Recruitment A/S recruiting on behalf of MSD in Copenhagen
Join MSD’s vaccines team and improve public health through partnerships and omni-channel customer engagement.
The Customer Manager Vaccines is the primary commercial point of contact in a designated area of vaccines and is accountable for the customer experience, coordinating internal resources and personnel to meet the needs of the customer.
In this role, you will 1) Develop long-lasting relationships with relevant specialists at hospitals and private clinics and identify and execute on opportunities for collaboration to improve public health and 2) Work closely with the regional organization to adapt & localize the brand strategies and ensure omni-channel customer engagement, including digital initiatives and appropriate non-promotional and promotional material.
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to join us in a challenging position as Senior Director for Global Clinical Operations? If you create results through leadership – you are our new Senior Director.
We offer an exciting position within a dedicated company, which is characterized by high quality, result orientation and speedy realization of the goals. You will be given the opportunity to have a high degree of influence and put your mark on the job, for personal and professional development.
As the company is growing; we are looking for a skilled, experienced and innovative Senior Director to drive Clinical Operations in Copenhagen.
- Leadership of the Global Clinical Operations group to achieve high performing teams
- Member of the Clinical Operations’ management team and influence on the strategy and execution
Ferring Pharmaceuticals A/S, Copenhagen
As Clinical Project Leader (CPL) you are part of the Global Clinical Operations team, currently consisting of approx. 50 experienced and highly dedicated persons (CPLs, Trial Managers, Document Managers and a Clinical Project Coordinator).
The CPL is representing Global Clinical Operations as core member of the Global Project teams. The CPL is responsible for delivering tactical and strategic input to the development plans and ensure the most appropriate clinical program is planned and conducted. The CPL works closely with the global project teams, therapeutic area functions, medical writing and trial management teams to deliver excellent clinical results to plan. The successful CPL will be the trusted clinical expert, be efficient in stakeholder management, develop and ensure project standards, and be confident in working with empowered trial teams.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
Work in the CMC Regulatory Affairs area within an exciting and fast growing biotech company
Genmab has a robust pipeline of innovative human antibody therapeutics and a number of strategic partnerships are already in place with international blue chip companies.
As CMC Regulatory Affairs Manager, you will be responsible for operational and strategic regulatory input with an emphasis on CMC matters to support worldwide development and commercialization of the Genmab pipeline. You will be part of the operational teams directing and coordinating international regulatory submissions supporting the conduct of clinical trials. Furthermore, you will be supporting marketing authorization submissions to EMA and other regulatory health authorities.
Hays Specialist Recruitment A/S recruiting on behalf of UCB
Unique position as Medical Science Liaison within immunology, covering Denmark and Norway.
UCB is a global biopharmaceutical company focused on the discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system.
This is an exciting opportunity to join the growing Scandinavian Immunology Team, and characterize the immunology therapy area publicly through scientific expertise. The function has developed rapidly during last years, and serves of vital importance for the organization. In the role, you will be provided with a high level of empowerment and achieve a close cooperation with key internal and external experts. It is an extrovert role, where you will spend approximately 60 % of your time externally focused.
Hays Specialist Recruitment A/S recruiting on behalf of MSD in Copenhagen
Do you dream of a global career in a company working to improve the lives of millions? When you join MSD, you become part of a community of inventors and creators committed to the same ambition: To invent and develop innovative pharmaceuticals – and to bring them to those that need them most. At MSD, your ideas, your talent and your experience will help change the lives of many.
In this role, you will be responsible for developing, leading and influencing the execution of the local franchise/launch plans for your therapeutic areas. You will coordinate with relevant cross-divisional stakeholders to ensure activities are aligned with MSD priorities and brand strategies and follow-up on KPI’s with tools and dashboards.
LEO Pharma, Ballerup
Arbejder du bedst med en høj grad af frihed under ansvar? Vil du have mulighed for at præge din egen hverdag og dine egne opgaver? Har du en forkærlighed for proces og teknik?
Som kemiker i Fucidin® API Purification kommer du til at fungere som bindeled og have daglig kontakt med mange forskellige faggrupper. Du skal supportere produktionen i tæt samarbejde med produktionsteknikere, smede og laboratorierne, samt koordinere processen ved uventede hændelser.
Ved hjælp af struktureret problemløsning skal du drive root cause analyser, udarbejde afvigelsesrapporter samt implementere forebyggende løsninger. Med tiden dygtiggør du dig i afdelingens procesanlæg og bliver dermed en kvalificeret sparringspartner for alle afdelingens interessenter.