77 hittade annonser
Elanco Denmark ApS, Herlev, Danmark
Elanco Animal Health söker en erfaren smådjursveterinär till tjänsten som Technical Consultant Companion Animals Nordics
Inför kommande lanserningar vill vi stärka upp vårt team med ytterligare en tekniskt konsult.
Du kommer att ingå i ett team bestående av tre tekniska konsulter som tillsammans ansvarar för den tekniska utbildning i de nordiska länderna, både intern utbildning av vårt sales team och extern support av våra kunder och samarbetspartners inom våra terapiområden, samt direkt produktrelaterad rådgivning. Arbetet innebär resor, framförallt inom de nordiska länderna, för att självständigt möta kunder eller tekniskt supportera säljarna. Du kommer också att hjälpa marknadavdelningen i deras arbete med att ta fram marknadsföringsmaterial för våra produkter.
Brinner du för att dela med dig av din fackkunskap och ditt intresse för livsmedelssäkerhet och matsvinn i storkök och livsmedelsproduktion?
Då är det dig vi söker för att stärka vår position på den svenska marknaden!
Dina primära arbetsuppgifter blir att stå för rådgivning och implementering gentemot våra svenska kunder på områdena livsmedelsproduktion, riskbedömning, egenkontroll och matsvinn i det digitala köket.
Bayer A/S, Copenhagen
Do you want to work with global regulatory strategies, a large and diverse product portfolio and interact with all the different Nordic authorities? Then you might be our new Nordic Regulatory Affairs and Pharmacovigilance Officer at Bayer Animal Health.
We are looking for a Regulatory and Pharmacovigilance Officer for a permanent position within Regulatory Affairs. The position is based in our Danish office in Copenhagen, Ørestad.
With reference to the Nordic Head of Regulatory Affairs you will be responsible for obtaining and maintaining marketing authorisations for your own product portfolio in all the Nordic countries. You will be in continuous contact with our global regulatory department in Germany, the local Bayer Nordic Animal Health organisation and the Nordic authorities.
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to join us in a challenging position as Lead Clinical Trial Manager in the Clinical Pharmacology Execution team within Global Clinical Operations?
You can expect to be working towards achieving the highest standards of current practice to fulfill the company’s needs for clinical data acceptable worldwide.
Your essential tasks will be:
- Plan, deliver and manage the clinical pharmacology trials from start-up to closure, in close collaboration with Translational Medicine
- Lead the clinical trial team to coordinate and manage all trial related activities
- Select and manage Phase 1 Units and other collaborators internationally
- Develop the operational plan and risk management plan for the conduct of the clinical trials
PharmaRelations ApS søger for Edwards Lifesciences
PharmaRelations søger på vegne af Edward Lifesciences en Account Manager til at varetage salget og markedsbearbejdningen af markedet for Critical Care i hele Danmark.
Du vil få en nøglerolle med at etablere og udbygge Edwards' stilling på markedet for perioperativ behandling/critical care.
- Etablere og udbygge relationer med kundegruppen som er ledende anæstesiologer, kirurger, intensiv og opvågningsafsnit samt indkøbere og hospitalsledelsen
- Vækste produkter og markedsandele i Edwards Critical Care portfolio
- Udvikle Business-, Account- og Actionplaner for området
Chr. Hansen A/S, Hørsholm
Vil du være med til at producere oste af høj kvalitet?
Helt overordnet er dit mål at være med til at udvikle så gode og ensartede oste, som det overhovedet er muligt. Du kommer til at arbejde med de fleste ostetyper og med kollegaer og kunder fra hele verden. Vores forsøg skal gøre os klogere på, hvordan Chr. Hansens ingredienser virker bedst muligt i forskellige oste og til forskellige kunder.
Dine primære arbejdsopgaver i stillingen bliver at:
- Medvirke til produktion af alle typer af oste i vores professionelle forsøgsmejeri (10-150 L skala)
- Gennemføre mælkeforberedelse inkl. standardisering og fremstilling af proteinkoncentrat m.v.
Chr. Hansen A/S, Hørsholm
In our Stability & Technology department you will reinforce the existing team of 7 competent and engaged colleagues working in a creative environment. The department cooperates with customers, colleagues, universities and research institutes both nationally and internationally.
This is an outstanding and unique scientific position where your responsibilities will count:
- Set the standards for formulation technology of bacterial cultures at Chr. Hansen
- Formulating and stabilizing bacterial cultures for multiple applications
- Conducting downstream processing studies, validation activities, and characterization activities of biologic products
We work in cross-functional projects, therefore responsibility, engagement and team playing are core values for you – as it is for us
We are looking for a Principal Scientist with a strong research background in psychiatric disorders and molecular biology training to join the Lundbeck Research Neuroscience organization in the department for Signal Transduction. As part of the larger Lundbeck R&D organization, we are focused on utilizing molecular and cellular neuroscience to establish the pharmacodynamic mechanisms of drug candidates at the cellular level and to continuously develop our understanding of disease biology and therapeutic entry points.
Your job and key responsibilities
- With your in-depth understanding of psychiatric disorders and with your firm grasp of genetics, molecular and cellular biology you will contribute with scientific leadership and key experimental data to guide and ensure the progression of drug discovery projects.
Do you have profound experience with regulatory CMC for biopharmaceuticals? Would you like to share your experience and be part of building up expertise within biopharmaceuticals across Lundbeck? Then you might be the new colleague we are looking for.
Lundbeck has traditionally worked with small molecules, but we are now also aiming to develop the competences necessary to be a key player in development of biopharmaceuticals (such as monoclonal antibodies). You will have a key role in this new strategy.
In your new job, you will be:
- Responsible for all Regulatory CMC activities on biopharmaceuticals development Projects
- Responsible for developing the Regulatory CMC strategy for assigned Projects
Statens Serum Institut, København
Er du dygtig til organisering og analyse af –omics data? Har du lyst til at være en del af forskningen på Statens Serum Institut? Så er du måske vores nye medarbejder.
Vi genererer forskellige typer af data fra vores kohorte-studier, primært multiplex protein, metabolomics, epi-genetiske og genetiske data, der gennem kombination med registerdata og biologisk/farmakologisk/medicinsk/biokemisk viden fører til opdagelse af nye biomarkører for medfødte sygdomme.
Vi søger en dygtig biostatistiker/bioinformatiker eller lignende, der sammen med vores eksperter indenfor biokemi, farmakologi og medicin, vil hjælp os med at udnytte det fulde potentiale af vores data og videreudvikle forskningen i afdelingen.
LEO Pharma, Ballerup
Biopharmaceutical Processes is looking for a Senior Scientist to work on late stage biologics projects (mainly mAbs) where you will be responsible for the drug substance part in the CMC team. You will review process changes and help prepare regulatory documentation in close collaboration with internal and external stakeholders. In addition, there will be opportunities to participate in projects in discovery / early stage as well as supporting established commercial biological products.
You will be working across in-house laboratory activities, guidance of external partners and CMOs for the manufacturing supply and tech transfer to external (CMOs) of drug substance. Review and write sections of Module 3 documentation, review and contribute to protocol and report writing.
The Regulatory Submission Management & Telematics Department is responsible for the critical operational activities relating to compilation and submission of marketing authorisation applications, regulatory data management and implementation of labelling and manufacturing changes in the production area.
Lundbeck Regulatory Information System (RIMS – ArisGlobal Register) is used for tracking information regarding Lundbeck's registered drug products globally. The system is used throughout the organisation in relation to e.g. life cycle management and release of products.
As Regulatory Data Manager, your main responsibility areas will be:
- Data entry
- Data quality activities
- Daily support and problem resolution for end users
LEO Pharma, Ballerup
Do you have solid experience within in vivo pharmacology, and are you looking for a job with major responsibilities, impact and exciting scientific challenges? Then our job as Principal Scientist is just right for you. In the department of In Vivo Biology and Safety, your primary role will be to enable progression of our drug discovery projects by generating the right in vivo pharmacology data.
The major focus of this position will be to evaluate the in vivo effect of novel therapeutic agents for inflammatory skin diseases. Your primary tasks will be:
- Define and plan the in vivo pharmacology deliverables for drug discovery Projects
- Design, monitor, interpret and communicate data from in vivo pharmacology studies, conducted either at LEO Pharma or by external CROs, in compliance with 3R principles
AGC Biologics A/S, Søborg
Are you passionate about leadership within a pharmaceutical company in rapid grow? Join a dynamic and international company where everyone is responsible for delivering right on time as one team!
As the Team Leader for the Downstream/Purification team you will be the direct leader of 11 technicians and two scientists. It will be your responsibility to people manage these people on an operational level in accordance with production schedule. People management, planning- and coordination of work, conducting mid- and end year appraisals, hiring people, secure prober training are in place, conducting board meetings, process confirmation on the shop floor and optimization of work processes in general will be some of the tasks that you will be responsible for.
Albright Life Sciences A/S recruiting on the behalf of AJ Vaccines in Copenhagen
Would you like to challenge yourself and daily see the value and impact of your deliverables through building key customer relations and sales through distributors delivering high quality vaccines that fulfil a global public health mission? Then come join the Sales & Marketing Team as Regional Sales Manager.
Your main responsibility will be to build customer relations and sales through distributors operating in a tender-based and special permit market while supporting, training, motivating and developing them and their sales teams to meet strategic growth- and revenue goals.
Our Sales and Marketing Department currently employs 10 people. Our activities cover all aspects of Sales, Marketing and also includes Shipping. Travelling: 50-60 days yearly is expected.
VAR2 Pharmaceuticals ApS, Copenhagen
If you like to work in the international biotech business and become a significant contributor to the building of a young Danish company, this might be the job for you!
You will join a group of ambitious scientists that work hard to bring innovative new cancer therapies and diagnostic methods to clinical testing within the next couple of years. To succeed with our ambitions, we are now looking for a new colleague that can help us create the necessary infrastructure and progress development projects and other important activities according to our plans.
As Project Coordinator you will work closely with the management team and project groups. In this role you will primarily work with project management tools to support the entire organisation in both the planning and execution of the development projects as well as implementation and follow-up of management tasks and processes.
GCP-enheden i København søger en GCP-koordinator 1. april 2019 i et et-årigt vikariat til monitorering af kliniske lægemiddelforsøg på Region Hovedstadens og Region Sjællands hospitaler.
Har du lyst til et job, hvor du
- tilrettelægger og udfører den lovpligtige monitorering af offentlige kliniske lægemiddelforsøg inden for alle specialer og med mange samarbejdspartnere.
- vejleder og underviser forskere og projektpersonale i ICH-GCP og national lovgivning på området.
- deltager i nationalt samarbejde om monitorering og udvikling af nye tiltag i forhold til kvalitetssikring af offentlige lægemiddelforsøg
- deltager i udvikling og vedligeholdelse af procedurer for vores arbejdsfunktioner
Y-mAbs Therapeutics A/S, Hørsholm
A new position is now open! Y-mAbs Therapeutics A/S (Y-mAbs) is looking for a CMC Project Manager. You will primarily focus on CMC activities associated with our late stage biologic development programs, and you will work with close interfaces to other functional groups within Y-mAbs. A good understanding of the outsourcing process, from quotations and contract negotiations to follow-up and troubleshooting with our CMC partners is a key competence as all manufacturing is outsourced.
It is key that you have in depth expertise within one of the following areas:
- Specific knowledge about drug product development in late stage development programs including commercial launch
- Formulation development of biologics – knowledge about sub-cutaneous formulations will be an advantage
- Solid experience in working with CMO/CRO's and international regulatory bodies like FDA and EMA
We are looking to add a new Senior Specialist with strong experience within upstream process development and manufacturing to our CMC Biologics team. The team is responsible for the strategic and technical leadership of pharmaceutical development activities in support of our biologics pipeline – spanning from pre-IND stage through process validation and launch.
As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.
LEO Pharma, Ballerup
Are you passionate about creating a compliant environment while optimising business performance?? Do you want to ensure compliance in our collaborations with healthcare professionals (HCPs) and healthcare organisations (HCOs)?
As Senior Healthcare Compliance Specialist you are a highly valued partner to the business supporting the global LEO Pharma organisation in HCP/HCO engagements. Your knowledge of and advice on the internal policies and applicable laws, regulations and ethical standards for engaging HCPs/HCOs is a cornerstone in securing that the business is compliant in collaborating with HCPs and HCOs.
Unique Human Capital recruiting on behalf of Orphazyme A/S in Copenhagen
Make a difference in a progressive and innovative biopharmaceutical company
Orphazyme is a very ambitious and visionary company. The company has had a good and well-paced growth during several years meaning that they are very much in control of their business and have well driven processes.
As Head of Clinical Operations at Orphazyme you will have the overall responsibility for the delivery of the clinical trial pipeline. You will be accountable for managing the clinical operations resources ensuring efficient and effective allocation enabling delivery of the trials.
The Head of Clinical Operations position is based in the Department of Clinical Development. The department is responsible for formulating, overseeing and directing clinical development activities, typically with the assistance of CROs.
Aureum A/S, Copenhagen
On 1 January 2018, the act on the medicinal cannabis pilot programme entered into force. Hence, a special development scheme for the cultivation and manufacturing of medicinal cannabis was introduced. The Danish Medicines Agency regularly issues cannabis cultivation- and production licenses with the purpose of supplying cannabis intermediate products to the pilot programme.
As Quality Professional you will be responsible for ensuring manufacturing of oils are in compliance with European GMP. Your job will cover a wide range of responsibilities, among other tasks:
- Assisting in designing the company’s Quality Management System.
- Authoring, reviewing and approval of SOP’s, Forms and Templates.
- Support in qualification and validation activities in relation to implementation and maintenance of manufacturing equipment and facility – including utilities and QC equipment.
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.
LEO Pharma, Ballerup
LEO Pharma has embarked on a very ambitious journey to become the world’s preferred dermatology care partner – and that is why we need you. If you can assure quality for clinical trials in order to safeguard subjects’ safety and well-being, you are the one we are looking for.
You will be GCP Lead auditor and will plan, perform, report internal and external audits 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 GCP auditor you will perform audits of clinical sites, laboratories and CRO’s located worldwide and be able to travel minimum 40 days per year worldwide.
Radiometer Medical ApS, Brønshøj
Har du minimum 3 års erfaring fra pharma eller life science indenfor labeling? Forstår du vigtigheden af compliance og den krævende regulatoriske verden? Kan du levere den præcise labeltekst, der er brug for?
Så kan du være vores nye labelspecialist, der supporterer Radiometers mange afdelinger i Danmark og udlandet og på den måde bidrager til Radiometers mission om at hjælpe sundhedspersonale til at træffe diagnostiske beslutninger, der redder liv.
Forvent en travl hverdag med mange henvendelser, hvor du fungerer som sparringpartner i forhold til den grafiske udarbejdelse af de påkrævede labels. Nogle af dine kerneområder er, at
- udarbejde og opdatere labels
- udarbejde projektplaner gerne i MS projekt
- oprette ECO (Engineering Change Orders) og sende til godkendelse