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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.

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.

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.

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.

Sommervikar til laboratoriet

Tican Fresh Meat A/S, Thisted, søger en sommerferievikar til laboratoriet, gerne med opstart hurtigst muligt.

Du behøver ikke være uddannet laborant eller have erfaring inden for laboratoriearbejde – du får en meget grundig oplæring.

Jobbet indebærer at forberede trikinanalyser, hjælpe med fremstilling af substrater samt diverse ad hoc-opgaver.

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

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.

Sundhedsvidenskabelige specialister til arbejdet med HTA-forordningen (genopslag)

Har du lyst til at være med til at sætte den danske retning for implementering af HTA-forordningen, så er det måske dig vi søger i Lægemiddelstyrelsen til to nyoprettede stillinger!

Din dagligdag i denne stilling vil være både dynamisk, udfordrende og præget af meningsfulde opgaver. Du får chancen for at sætte dit præg på både det danske og europæiske arbejde med HTA forordningen. Et arbejde, der kommer til at få stor betydning for de danske HTA-organisationer, virksomheder og patienter.

Vi mener, at der skal være en god balance mellem arbejde og fritid, derfor tilbyder vi en stilling på 37 timer med mulighed for at arbejde hjemmefra.

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.

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.

Project Manager

Som Project Manager på fabrikken i Hobro vil dit job være opdelt i en projektlederrolle, og en rolle der dækker daglige driftsopgaver.

Du både deltager i og leder selvstændigt større projekter relateret til fabrikkens anlæg og udstyr - fx lokaleombygning, installation af ventilationsanlæg, dokumentation etc. Du skal planlægge og udføre projekter fra start til slut, herunder sikre at tidsplaner og budgetter overholdes, være primær kontakt til myndigheder og eksterne samarbejdspartnere samt udføre, lede og koordinere arbejdet i projekt teamet, så projekterne kommer godt i mål.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Quality & Compliance Manager

Are you passionate about quality and decency, and do you want to hold a key position in a growing sound international company focused on sustainability? Then you should read on.

You will be a part of the global supply chain organization in Middelfart and report to COO. The area of responsibility is material quality, compliance, and risk management, and you will be the driver of creating a culture of continual improvement by identifying opportunities for efficiency and innovation within the quality and compliance area with a focus on sustainability and the global ESG agenda.