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We are looking to add a new CMC Biologics Project Manager 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 pre-IND stage through validation and launch. As CMC Biologics Project Manager, you will lead the development of drug substance for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.
Your job and key responsibilities:
Be an active player in the development and execution of the project specific CMC strategy and operational plans taking all the CMC development phases towards successful BLA into consideration
Arla Foods, Vojens
Vil du være med til at drive udviklingen og optimeringen af Arlas mejeri i Høgelund ved Vojens? Har du god erfaring med projektledelse og fortrolig med LEAN-principperne?
Som projektleder er du ansvarlig for både at optimere den daglige drift og håndtere det løbende udviklings- og forbedringsarbejde af anlæg, processer og produktkvalitet blandt andet ved hjælp af LEAN-værktøjer. Du kommer til at indgå i et bredt samarbejde med dygtige kolleger på alle niveauer af organisationen herunder også markedsorienteret fokus med kunder og vores Product Management.
Dine vigtigste opgaver inkluderer:
- projektledelse af udviklings- og forbedringsprojekter fra ide til implementering af nye maskiner, produkter og emballager
- opsøge nye leverandører samt indkøb og forhandling af leverandørkontrakter
We are looking for a highly motivated research assistant to join the discovery of new innovative treatments for brain disorders. The Department of Molecular Screening is responsible for molecular pharmacology and screening support for Lundbeck’s drug discovery projects. Techniques represented in the Department include molecular pharmacology, electrophysiology and various cell-based and biochemical assays to profile small molecules and biologics.
You will be part of a team providing molecular pharmacology and screening support for research projects aiming for new drug candidates for psychiatric and neurological diseases. You will be responsible for planning and executing studies and reporting these to project teams.
SOS International a/s, Frederiksberg
Vil du være en del af en spændende, international arbejdsplads, hvor du har mulighed for at hjælpe og gøre en forskel for skandinaviske patienter over hele verden?
SOS International assisterer skandinaviske rejsende overalt i verden på vegne af forsikringsselskaber. Det sker via vores døgnåbne alarmcentral 24 timer i døgnet – 365 dage om året.
Vi søger en kollega til Transport Centeret med specialefunktion som SAS Medical Assistance. Stillingens primære formål er at godkende og planlægge medicinske transporter for SAS samt andre flyselskaber, som SAS har kontrakt med. Dette gøres ved medicinsk at vurdere de sager, som kunderne/forsikringsselskaberne sender til SAS og derefter bestille/arrangere transporten med det nødvendige udstyr og assistance.
3Shape A/S, Copenhagen
Are you ready to pursue your scientific career within digital health working with 3D scanners as well as software medical devices in a global setting? Then 3Shape offers a unique opportunity to work as a Scientific Manager in the center of Copenhagen at Kongens Nytorv.
The main purpose of the job is to develop and maintain our clinical evidence documentation as well as to facilitate post market activities in order to support our products with regards to safety and clinical performance as well as claims. You will be cooperating with multiple stakeholders internally as well as externally.
Job responsibilities include:
- Preparation and maintenance of Clinical Evaluation Reports (CERs)
- Ensure that the clinical evidence requirements and the CERs for our products comply with current and future global medical device guidance and regulations
3Shape A/S, Copenhagen
Are you ready to continue your regulatory career within digital health working with 3D scanners as well as software medical devices in a global setting? Then 3Shape offers a unique opportunity to work as our new Regulatory Affairs Specialist in the center of Copenhagen at Kongens Nytorv. This opportunity will help you develop within future disruptive health technologies together with the entire organization and with exposure to senior management.
As a Regulatory Affairs Specialist, you will join our Global Regulatory Affairs team based in Copenhagen. We are currently a team of nine Regulatory Affairs Specialists/Coordinators and one Scientific Manager with diverse backgrounds. Six additional colleagues are expected to join the team in 2018. You will interact with a wide range of stakeholders and especially with R&D, Product Management, Global Sales offices, and external consultants worldwide.
Agilent Technologies Denmark, Glostrup
- Are you interested in making a difference in the field of cancer diagnostics with Agilent?
- Then we have the job for you!
- You will join a team of high skilled, enthusiastic colleagues in a dynamic company. The position is permanent and has a lot to offer.
We are looking for an experienced Quality Assurance Specialistto join a market leading Medical Device company Dako - Agilent technologies in a global support role. You will be an integral part of the Quality Assurance-Systems Engineering department and will have an opportunity to work with the field service global organization.
This is a unique opportunity to work in the field of medical technologies, where knowledge sharing and professional respect are combined to make it both fun and meaningful to go to work.
Sandoz A/S, Copenhagen
Do you want to work for a Global Pharmaceutical company where you will get recognized for your hard work and commitment? Look no further, apply today for Commercial Manager OTC. The Nordic OTC business is an important contributor of Sandoz future growth strategy, and is expected to grow significantly in the years to come.
The purpose of the Commercial Manager role is to lead the commercial sales activities towards pharmacy chain customers in Denmark, Sweden and Norway. In addition the Commercial Manager will also be sales manager for a field based sales force visiting pharmacies in Denmark. The Commercial Manager reports to Franchise Head OTC Nordics, and is end-to-end responsible for all commercial activities regarding the OTC portfolio in Denmark, Sweden and Norway.
Genmab A/S, Copenhagen
Genmab is an international biotechnology company specializing in the creation and development of differentiated human antibody therapeutics for the treatment of cancer.
Genmab is now searching for an experienced Clinical Development Coordinator to be part of global development at our Headquarters in Copenhagen. The work environment at Genmab is within a global setting and characterized by people empowerment, new challenges and devoted and talented colleagues.
In this newly established position your key responsibilities will be to:
- Work closely with and support the Head of Operations R&D and CPH based development function heads
- Produce and refine presentation materials
- Plan and structure meeting calendar
Join a team of highly-skilled Regulatory Affairs Professionals for 12 months.
ALK offers an exciting opportunity to work in their Global Regulatory Affairs (GRA) department with lots of interdisciplinary collaboration both internally and externally. GRA counts approximately 50 people and we are located in Hørsholm.
As Regulatory Affairs Professional you will be given a range of responsibilities within both regulatory Clinical, Non-Clinical and Procedural activities in ALK. You will work closely together with the top motivated team members of the RA-team. The team consists of 9 people including the manager of the team.
Agilent Technologies Denmark, Glostrup
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek – so they can do what they do best: improve the world around us.
Are you interested in working in the Medical Device industry and aiding in the treatment of cancer? Do you have a structured and proactive approach to work? Do you have great communication skills and drive?
You will be a part of a team responsible for the following activities:
- Customer complaint handling and surveillance
- Facilitate quality investigations and root cause analysis
- Facilitate critical product quality issues activities (NCR, DEV, CAPA)
BioPorto A/S, Hellerup
BioPorto Diagnostics A/S is an in-vitro diagnostics company that provides healthcare professionals in clinical and research settings a range of diagnostic tests and antibodies. Our pioneering product portfolio includes assays for underserved disease states such as NGAL for acute kidney injury.
We sell our products in more than 80 countries through diverse sales channels and partners. BioPorto has its headquarters in Copenhagen, Denmark and is listed on the Nasdaq Copenhagen stock exchange.
All our colleagues are committed and dedicated to commercializing the company’s diagnostic portfolio. If you aspire to be part of this organization, we are eager to hear from you.
Novozymes A/S, Bagsværd
Do words like quality, food safety, food defense, vulnerability assessment, management systems, standards, certifications, audits and data analysis catch your attention? If yes, then you might be our new colleague in the Quality Compliance Department, which is part of the Global Quality area.
You will be key in continuously improving Novozymes’ food and feed quality system in close collaboration with other quality colleagues in the food industry. With your in-depth knowledge of food certifications, you will play a key role in implementing new requirements from food standards globally.
Are you the next Zymer in our team? Consider a career with Novozymes and let’s realize your potential together.
Motiveres du af at sikre både simplificering og branding på store komplekse produktionsanlæg og enkeltmaskiner til chokolade-, bageri- og konfektureindustrien?
Som produktingeniør bliver du ansvarlig for, i samarbejde med f.eks. indkøb, marketing, salg, R&D og de produktansvarlige, at forbedre både design og dokumentation på tværs af vores produktserier. Du er med til at udvælge områder/delkomponenter med størst indflydelse og skal kunne præsentere og vurdere business casen i de ændringer, du indarbejder.
Opgaverne kan spænde fra udvælgelse af komponenter, der skal udskiftes til endelig implementering i design og standarddokumentation. Hertil kommer at støtte de produktansvarlige i, at vores standardpakker bliver optimalt stykket sammen ift. ensretning, optioner og komponentudskiftning.
This position reports to the Group Manager, of one of our dairy teams but will work across application groups, including sweet dairy, cheese, frozen desserts, beverage & bars and bakery.
The focus of this position will be to conduct applied research and product development with probiotic bacteria with an emphasis on customer support. You will work closely with other Innovation scientists on a project by project basis, but is also expected to be able to carry out experiments independently.
- Conduct applied research and product development with probiotic bacteria with an emphasis on cell count stability in a wide range of food and beverage systems.
- Solid understanding of the clinical trial data for each probiotic strain. Presentation of these data to Application, Sales and Customers.
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.
Vil du være med til at opbygge et ensartet kvalitetssystem, som skal strømline indkøbsprocessen for 8 forretningsenheder? Kan du samle input fra interessenter på tværs af værdikæden, finde frem til best practice og udforme procedurer, som skaber strategisk værdi og giver mening ude i forretningen?
Som specialist spiller du en aktiv rolle i at opbygge vores nye kvalitetssystem, der skal sikre ensartede processer. Derfor kommer du omkring alt fra leverandørstyring, specifikationsgodkendelse, reklamationsbehandling, IT-systemer og udførelse af interne og leverandøraudits.
Du får ansvar for flere underprojekter inklusive driftsmæssige og administrative opgaver, mens du:
- evaluerer og godkender leverandører
- foretager risikovurderinger
- udarbejder rapporter omkring leverandørperformance
AJ Vaccines A/S, København
Til QA Compliance søger vi en QA Senior Specialist, som vil indgå i et team med yderst kompetente kollegaer og som brænder for at vedligeholde og udvikle vores GMP kvalitetssystem. Som vores nye kollega får du muligheden for at arbejde med forskellige arbejdsopgaver indenfor compliance sammen med engagerede og motiverede kollegaer.
Med direkte reference til Head of QA Compliance vil dine arbejdsopgaver være indenfor nedenstående områder:
- At udarbejde, vurdere og godkende GMP-instruktioner
- At opbygge og vedligeholde kvalitetssystem, herunder udarbejde QA’s politikker, procedurer og instruktioner
- At deltage i selvinspektioner og egne inspektioner, herunder planlægning, udførelse og rapportering
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.
Glycom Manufacturing A/S, Esbjerg
Glycom Manufacturing i Esbjerg søger en barselsvikar for vores HS-manager fra 1. april 2018 og til 1. maj 2019. Med reference til underdirektøren får du ansvar for at drive og videreudvikle virksomhedens arbejdsmiljø og sikkerhedskultur. Du får ansvaret for at drive vores arbejdsmiljøorganisationsarbejde og sikre et godt samarbejde.
Du vil få til opgave at udarbejde operationelle procedurer og instruktioner og implementere disse. Din opgave vil også være at uddanne vores medarbejdere inden for arbejdsmiljø, sikkerhed og beredskab – herunder afholdelse af beredskabsøvelser og sikre løbende udvikling af beredskabsplanen.
- Den daglige sikkerhedsledelse
- Fremme en god rapporteringskultur
- Drive vores observationskortmøder