171 jobannoncer matcher din søgning 171 jobannoncer fundet

Nyuddannet proces, - eller industrioperatør til fermentering i medicinalproduktion hos Xellia

Er du teamplayer af natur og parat til nye udfordringer?

Som operatør vil dine primære arbejds- og ansvarsområder være:

• fyldning, sterilisering, podning, fermentering og høst
• overvågning og betjening af procesanlæg
• overvågning og betjening af forsyningsanlæg, herunder vandanlæg og nedbrydningsanlæg

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.

Formulation Scientist

Are you looking to use and grow your experience in formulation development in a broad role with independent responsibilities? Do you want to drive formulation projects and contribute to the strategic development of future products?

In this role, your overall focus will be formulation development of drug products. Your responsibilities will cover formulations used for toxicology and clinical studies through the development phases and all the way to the commercial drug product.

Site QEHS

Brænder du for at arbejder med QEHS, kan du godt lide at arbejde i et overskueligt team – så er du måske vores nye Site QEHS på vores site i Aabenraa? Du vil være tovholder på at implementere og opretholde kvalitets- og EHS standarder.

Dine ansvarsområder bliver udvikling og implementering af QEHS-strategier, -politikker og -mål i overensstemmelse med virksomhedens overordnede mål.

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

Scientific Consultant (project position) – DTU Health Tech

DTU Health Tech is seeking a formulation chemist to contribute to an exciting local depot formulation technology, CarboCell, e.g. for delivery of antibiotics aimed at local infection treatment.

This role is a unique blend of scientific research and commercial venture, involving work on patented technologies and a strategy for sustained release of small molecule-based therapies.

You will play a key role in evolving our research into a successful spin-out company.

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.

Glostrup Apotek Magistrel Produktion søger tablettekniker til job med høj grad af variation

Vi kan tilbyde en sjov, spændende og unik arbejdsplads. Har du lyst til hands-on produktion af en stor variation af tablet-produkter og med udpræget indflydelse på eget arbejde, har vi jobbet til dig.

Du kommer til at indgå i et team, hvor du primært skal være med til alle aspekter af tabletfremstilling herunder afvejning, fremstilling af granulater, opstilling af tabletmaskiner og komprimering.

Arbejdstiden vil ligge i tidsrummet mandag til fredag kl. 8-16 med fleksibel arbejdstid.

Operatører til AJ Vaccines søges

Er du omhyggelig, ansvarsfuld og har solid GMP-erfaring fra et produktionslignende miljø? Så er denne mulighed hos AJ Vaccines helt sikkert noget for dig!

Som operatør hos os kan du se frem til at indgå i en lang række forskellige produktionsprocesser. Afhængig af din tilknytning til virksomheden, vil du bl.a.:

• Administrere batchjournaler, inkl. udprintning og etiketproduktion.
• Udføre prøveudtagning og håndtere prøveafsendelse.
• Koordinere med håndværkere ved maskinproblemer.

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.

Experienced Scientist for validating QC methods in Novonesis

Do you want to work in an environment where great collaboration is valued as highly as scientific excellence?

Working as Scientist in our team, you will be responsible for validating and optimizing analytical methods for Human Health products in our QC labs. You will work closely with other scientists and laboratory technicians to plan and implement efficient microbiological methods.

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.

Lab Quality Coordinator, GCLP Laboratory

As Documentation Coordinator at the laboratory in Lund at MinervaX, you will play a central role in the establishment of a GCLP laboratory for clinical samples from MinervaX’s prophylactic vaccine targeting Group B Streptococcus (GBS). The GLCP laboratory is established to move into phase III clinical trials. You will be responsible for the writing, coordination, storage, and maintenance of documentation in the whole laboratory area.

This is a unique opportunity to join the journey into building a GLCP compliant laboratory. As this is a new position you can develop this role according to your own ambitions and will be primary person on documentation support.