154 jobannoncer matcher din søgning 154 jobannoncer fundet

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.

To inspektører til Miljøstyrelsens Kemikalieinspektion i Slagelse søges – en til kontrol på PFAS-området og en til kontrol på kosmetikområdet (faste stillinger)

Vil du arbejde med kontrol og håndhævelse inden for kemikalieområdet? Har du lyst til at indgå i et juridisk og kemisk-fagligt miljø af professionelle inspektører og håndhævelsesjurister, hvor vi lægger vægt på en målrettet kontrol og proportionel håndhævelse?

Så er et job som inspektør i Kemikalieinspektionen med fokus på hhv. PFAS eller kosmetik måske noget for dig.

Du vil hos Kemikalieinspektionen få en arbejdsplads med høj fleksibilitet, gode kolleger og med plads til læring og udvikling. Vi kan fx tilbyde mulighed for hjemmearbejde i op til to dage ugentligt.

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.

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.

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.

Skal du være vores nye lægesekretær?

Skal du være vores nye sekretær?

Vi søger en lægesekretær på 25-30 timer om ugen, fordelt på 5 dage.

Patientkontakt er kernen i dit arbejde sammen med dine to kolleger i sekretariatet. Du er fagligt nysgerrig og arbejder med en grundighed og følger opgaverne til dørs. Du trives med både administrative og praktiske opgaver. Du opsøger selv gode løsninger og er hjælpsom.

Vi værdsætter en alsidig og udfordrende hverdag med høj faglighed og plads til et godt grin i vores fælles frokostpause.

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.

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.

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.

Application Technologist

Tetra Pak Filtration Solutions is searching for an Application Technologist in the field of membrane filtration of milk and whey products, with the focus on optimizing the environment footprint and applications.

As an Application Technologist, your responsibilities will be:

• Planning, execution and documentation of technology and application testing at customers site and in our development center.
• Data collection from full scale systems in operation, with focus on optimizing system performance and membrane selection.

We offer you an equal opportunity employment experience that values diversity and inclusion Market competitive compensation and benefits with flexible working arrangements.

Laborant til meget velfungerende peptidkemi laboratorie

Som laborant i vores peptid laboratorie er dit og kollegernes fokus at skabe grundlaget for udvikling af nye lægemidler. Du giver dit vigtige bidrag ved at bruge størstedelen af din tid med at arbejde hands-on i vores state-of-the-art laboratorie.

Du får et meget alsidigt job med ekstraordinært gode muligheder for at lære nyt og udvikle dig. Du kommer til at udføre alle typer af opgaver fra betjening af robotter og forskellige instrumenter til vedligehold og procesoptimering. Du kommer også til at arbejde med databehandling og dokumentation.