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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.

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.

Konsulent til Team Rådgivning og Forhandling – vil du med på holdet?

Vi leder efter en ny kollega, som skal understøtte og rådgive vores medlemmer, og som har lyst til at blive en del af et sekretariat, der ser det som sin vigtigste opgave at styrke farmakonomernes rolle og hjælpe dem på bedste vis.

Din primære opgave vil være medlemsrådgivning og sagsbehandling - telefonisk og via mail. Det er en opgave som alle konsulenter deltager i løsningen af. Det er derfor vigtigt, at du trives med den direkte kontakt med medlemmerne.

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.

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.

PhD Formulation Innovation Scientist

Do you want to help us revolutionize an industry & build your experience with technologies intended to improve the bioavailability of BSC class II & IV drugs?

As our new formulation Scientist, you will specialize in the delivery of cannabinoids; you will play a vital role in our organization, being part of our early-phase development. You have a scientific and innovative mind-set and understand how to translate knowledge into new technological achievement in relation to delivery.

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.

Specialist til proces og teknologi

Vil du være med til at udvikle vores fabrik i Aulum?

Vi søger lige nu en engageret og selvstændig proces-/kemiingeniør eller tilsvarende til vores fabrik i Aulum, Midtjylland.

Hovedopgaven er produktionsprocesser og -optimeringer samt at udvikle produkter af høj standard, som matcher vores kunders efterspørgsel.

Du bliver del af en virksomhed, hvor der lægges mærke til din indsats, og hvor der er rig mulighed for faglig og personlig udvikling.

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.

Medical/Pharma Quality Assistant

Vi søger en engageret og ansvarsbevidst kvalitetsassistent til vores team hos Jetpak Danmark A/S. I denne rolle vil du arbejde tæt sammen med terminalchefen for at opretholde og forbedre vores kvalitets- og ledelsessystemer, specifikt inden for håndtering, pakning og distribution af medicin på vores GDP-certificerede lager i Kolding.

Hos Jetpak kan du forvente et inspirerende arbejdsmiljø med dygtige kolleger, frihed under ansvar og mulighed for at være fleksibel. Vi tilbyder kontorplads på vores Road hovedkontor i Kolding, og arbejdstiden er typisk fra kl. 8 – 16, med plads til fleksibilitet.

Veterinær til Husdyr Innovation

Er du dyrlæge, og brænder du for at gøre en forskel for dansk griseproduktion?

Som dyrlæge i afdelingen Husdyr, Gris, bliver du en vigtig kollega indenfor innovation og udvikling vedrørende grisens sygdomme, sundhed, smittebeskyttelse, velfærd m.m. Du bliver ansvarlig for projekter lige fra planlægning til den praktiske gennemførelse og afrapportering.

Afhængigt af hvor du bor, vil du have kontorplads enten i Agro Food Park i Skejby eller på Axelborg i København.