12 jobannoncer matcher din søgning 12 jobannoncer fundet

Supporter til produktionsforbedringer og drift

Vil du være med til at bekæmpe kræft?

Brænder du for at lave forbedringer af processer og produktionsfaciliteter, samtidig med, at produktionen holdes kørende?

Dine opgaver vil være at stå for store og små procesforbedringer. Det kan være mindre tilretninger af SOP’er eller store forandringer som fundamentalt ændrer vores måde at arbejde på.

Vi tilbyder masser af ansvar og indflydelse på dine arbejdsopgaver.

Akademiker til daglig support og procesforbedringer

Vil du være med til at bekæmpe kræft? Brænder du for at lave forbedringer der sikrer høj kvalitet? Er du klar til at gøre en forskel for dine kolleger og forbedre produktionsfaciliteterne til gavn for Agilents kunder?

Dit hovedansvar vil være at sikre GMP-niveauet i produktionen. Du vil i den forbindelse skulle afklare GMP-spørgsmål samt udarbejde Non-Conformance Reports (NCRs).

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.

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.

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.

Entrepreneurial Immunologist for Applied Research

Would you like to be part of an exciting journey of generating scientific insights on the health effects of human milk oligosaccharides (HMOs), in addition to further improving infant formulas by bringing them closer to breastmilk?

As our senior immunologist, you will be a key member of the Applied HMOs team by leading our immunology platform. Your primary role will be to ensure a strong platform both by running existing in vitro assays and by establishing novel experimental immunological workflows. You will work closely with our commercial team and will also be involved in meetings with customers.

QA Assistant

Motiveres du af en stilling, hvor du har fokus på systemer og kvalitet? Og vil du arbejde med fremstilling af pakkematerialer til den farmaceutiske industri?

Du vil få daglig sparring med operatører, specialister og ingeniører i vores produktionsenhed i Horsens – som årligt producerer ca. 2,5 milliarder enheder.

Vi tilbyder en spændende stilling med mulighed for at sætte dit personlige præg på måden, tingene fremadrettet skal gøres på.

Clinical Trial Assistant

Are you looking for the possibility to unfold your competences within clinical operations even further? Do you thrive in an innovative environment working alongside dedicated clinical research professionals? Are you a self-driven team player, who enjoys a varied and influential day at work?

Pharmacosmos A/S is a progressive and innovative pharmaceutical company with headquarters in Holbæk, Denmark. We are on an exciting journey of global growth inventing new and innovative treatments, and right now we are expanding our team with a Clinical Trial Assistant.

Specialist, Regulatory Affairs (Temporary Position)

As Regulatory Affairs Specialist, you will be responsible for lifecycle management of products manufactured at Orifarm’s own manufacturing sites. Therefore, you will collaborate closely with colleagues across functions, such as chemists, formulation specialists and co-workers within Quality, Supply Chain, Manufacturing and Sales.

Further, your main responsibilities include to:

• Gather information and documentation for variation applications
• Update dossier sections

Creative Assistant

Are you inspired to contribute your expertise to a global leading Flavors Organization? Are you passionate in working in a dynamic team with creative and empowered people?

Your Focus will be:

• Always following correct compounding procedures
• Prepare compounded flavors for evaluation, including preparation and running of difference testing if project requires.
• Coordinate with QC to obtain specifications of all experimental recipes within 24 hours of completion of evaluation.