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QA Assistant, GS-5, QAC
This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.
The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.
Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Global Regulatory Specialist, Plant Health (temporary position)
As Regulatory Affairs Specialist you will be part of the Global Regulatory Affairs team, with around 18 team members across the globe. You will work closely with stakeholders in the Plant Health industry and support the execution on regulatory strategies globally.
You will interact with cross-functional product and project groups and maintain close interaction with stakeholders in biotechnology, other parts of R&D, sales, marketing and with strategic customers and authorities.
Farm Sustainability Manager - Aarhus
Do you have insights in agrobiology, biodiversity and a beating heart for nature and dairy?
In this role you will be the center of knowledge sharing among our farmer owners and a lighthouse for inspiring to sustainable actions focusing on crop nutrition, soil, natural areas and biodiversity.
You will facilitate meetings to inspire farmer-owners to investigate and make climate actions and become a relevant part of the strategy at farm level.
Project Manager PMO - Medical Devices
We are looking for an experienced Project Manager to join our Technology and Innovation PMO organisation.
You will lead multidisciplinary teams of engineers and specialists, applying your project management, people leadership, and technical skills to develop new products, variants or upgrades.
Application Food Technologist
Trives du med at udvikle nye applikationer og teste produkter og er vant til at præsentere resultater for interne som eksterne kunder fra mange nationaliteter, så er dette job måske lige noget for dig?
Du vil få et bredt ansvarsområde med varetagelse af opgaver i forbindelse med udvikling og dokumentation af nye metoder og applikationer samt vedligeholdelse og opdatering af eksisterende applikationer inden for kødsegmentet. Derudover skal du bl.a.:
- supportere salgsafdelingen
- foretage og dokumentere div. tests og analyser
- supportere inden for innovative tiltag
Produkttilpasser & -udvikler
Har du erfaring med produktudvikling inden for fødevarer? Brænder du for at arbejde med smage og konsistenser? Vil du optimere og udvikle nogle af Danskernes foretrukne hverdagsbrands?
Du skal med afsæt i produktchefens brief optimere eksisterende produkter og udvikle nye til Stryhns Gruppens produktportefølje, som produceres på vores 5 danske fabrikker. Dit hovedfokus bliver på vores postejfabrik i Roskilde.
GoodLife Foods i Nyborg søger medarbejdere til produktion og pakning af vores Daloon forårsruller
Vi har travlt hos GoodLife Foods. Så travlt, at vi skal have styrket vores produktion med engagerede produktionsmedarbejdere.
GoodLife Foods producerer og sælger et bredt sortiment af forskellige sunde forårsruller, som er produceret med friske råvarer heriblandt de kendte Daloon forårsruller.
Stillingerne omfatter følgende arbejdsopgaver:
- Primært maskinelle processer, drift af rullemaskiner hvor vi fremstiller forårsrullerne
- Vores pakkeri, hvor avancerede pakkeanlæg skal passes
Kundeservicekonsulent til Nomeco HealthCare Logistics – barselsvikariat
Brænder du for kundeservice, lægemidler og logistik? Vil du være en del af en stor international virksomhed, som arbejder med sundhedslogistik?
I Nomeco HealthCare Logistics søger vi en serviceminded kundeservicekonsulent til vores SygehusService-team. Der er tale om et barselsvikariat på fuld tid, der løber indtil maj 2025.
SygehusService sidder i Sydhavnen. Herfra vil du, sammen med gode kolleger, hver dag gå forrest for at yde den bedste service til alle landets sygehusapoteker og andre sygehuskunder.
Sales Manager
Are you ready to drive sales in the world's first and only partner within three innovative solutions for freezing, cooling and heating?
Your primary responsibility is to drive growth in the Scandinavian markets across the entire product range, leveraging networking skills to establish fruitful relationships and expand the client base within the food industry.
You will use the initial learning period to lay a solid foundation for future success, including understanding the product range, market dynamics, and internal processes. After some time, you will have autonomy over own budget and have significant influence in crafting the sales strategy, ensuring alignment with company goals.
Laborant QC Sampleflow
Har du laboratorieerfaring og kunne du tænke dig at tage det næste skridt i din karriere?
Du får ansvar for og stor medbestemmelse over dine opgaver så de fleste dage vil gå stærkt, og opgaverne bliver ofte andre end dem, du havde planlagt og forventet.
Du vil opleve en dynamisk og udfordrende hverdag i QC, med mange spændende opgaver og en åbenhed over for nye idéer.
Project Manager
Do you have experience in driving technical projects and want to be part of a company on an exciting growth track?
You will contribute to projects ranging from new equipment lines to the replacement of existing equipment and systems. As a Project Manager, you will lead projects or be responsible for and execute work packages or tracks, depending on project size.
Project Coordinator
Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?
As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.
Operators for Drug Product Manufacturing
Would you like to be part of an international pharmaceutical company in rapid growth, which offers good development opportunities and set shifts?
This project is in the early phase of establishment and in the beginning, you will help design and establish processes for the upcoming production.
Main tasks:
- Participate in running and validation of equipment on site
- Assist during installation of equipment on site and carry out qualification tests afterwards
Clinical Supply IRT/RTSM Specialist
Come help us deliver high-quality clinical trial supply to trials all over the world
We are looking for an IRT/RTSM specialist to help us ensure timely setup of IRT/RTSM systems to support the delivery of trial supply for Ferring clinical programs globally.
In this role you are expected to not only collaborate closely with cross-functional teams but also contribute to a knowledge-sharing mindset and promote a collaborative and innovative work environment. You must have a flair for respectful communication with a range of stakeholders such as Clinical Operations, IT and Quality Assurance.
Operations Data Coordinator for Drug Substance Production
The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.
You will be part of a team with a great sense of humor and a high willingness to support where needed.
QA Specialist for Environmental Support
In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).
This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.
2 Regulatory and Marketing Compliance Managers
Har du interesse for og meget gerne erfaring med Regulatory Affairs – og helt optimalt med Marketing Compliance – og vil du gerne arbejde mere målrettet med Marketing Compliance?
Dine arbejdsopgaver bliver bl.a.:
- Compliance review af marketingaktiviteter og -materialer for den farmaceutiske industri og anmeldelser til Etisk Nævn for Lægemiddelindustrien
- Oversættelser af regulatoriske og medicinske dokumenter (dansk/engelsk)
- Andre regulatoriske opgaver svarende til opgaverne i et dansk datterselskab: gennemgang og opdatering af produktinformation, regulatorisk review af artwork m.v.
Senior Process Specialist
Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.
You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.
Scientist for Biomarker Assays
Are you eager to use your scientific skills and expertise in preclinical research?
As our new scientist, your tasks will include:
- Coordination and support of biomarker experiments, including supervision of lab technicians.
- Perform data analysis, interpretation, review, and reporting of study results.
- Development of new biochemical- and immunoassays and troubleshooting of existing assays.