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Energisk laborantvikar til spændende QC-opgaver

Som laborantvikar vil du indgå i et team af engagerede og dygtige kolleger, der varetager kvalitetskontrol af råvarer, mellemprodukter og færdigvarer samt analyseudvikling og analyse af stabilitetsforsøg, samt diverse praktiske og administrative opgaver.

Du vil komme til at arbejde med kemiske analyser under anvendelse af interne instrukser. Det anvendte udstyr er primært HPLC, spektrofotometre, Mastersizer, ICP-MS samt en del mindre udstyr. Der arbejdes efter GMP og med et højt kvalitetsniveau.

Laborant QC Sampleflow

Har du laboratorieerfaring og kunne du tænke dig at tage det næste skridt i din karriere?

Du får ansvar for og stor medbestemmelse over dine opgaver så de fleste dage vil gå stærkt, og opgaverne bliver ofte andre end dem, du havde planlagt og forventet.

Du vil opleve en dynamisk og udfordrende hverdag i QC, med mange spændende opgaver og en åbenhed over for nye idéer.

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.

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.

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.

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.

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.

QA Ext. Manufacturing Specialist

Would you like to work in one of the most interesting, complex, and dynamic areas in Bavarian Nordic? Are you ready to engage, support, and mobilize colleagues in a growing international business environment where we focus on saving lives every day?

As a QA Specialist, you will be responsible for daily support, QA oversight, and GMP guidance to Contract Manufacturing Organizations (CMOs) to ensure that our products are manufactured according to current GMP and our marketing authorizations.

Laborant til analyse af mellemvarer og færdigvarer

Vi søger en laborant eller tilsvarende til vores kvalitetslaboratorium, hvor det primære ansvar vil være analyser af mellemvarer og færdigvarer samt vedligehold af laboratoriedriften. Du vil i samarbejde med kollegaer og teamleder, bidrage til laboratoriets leverancer, der primært er fokuseret mod driften. Vi arbejder med forskellige kemiske analysemetoder, hvor HPLC er det primære analysesystem.

Du vil komme ind i et dynamisk laboratorie, hvor dag-til-dag ændringer må forventes at komme; samtidig vil der være rutineopgaver, da der er tale om et driftslaboratorie.

Tekniker til et af verdens førende halvleder- og fabrikationslaboratorier

Laboratoriet er et af Europas største, og her får du en helt unik mulighed for at blive en del af et dynamisk og internationalt miljø bestående af forskere, ingeniører og specialister, der forsøger at skabe helt nye og banebrydende teknologier.

Dette forskningsprogram er fordelt på 7 laboratorier på tværs af 3 kontinenter.

Som tekniker kommer du til at spille en afgørende rolle ift. at sikre at laboratoriet er operationelt, og at udstyr altid fungerer efter hensigten.

Lab Maintenance Technician

We are looking for a Lab Maintenance Technician for our client’s brand-new semiconductor and fabrication laboratory in Copenhagen.

The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.

As a Lab Maintenance Technician, you will play a crucial role in making sure that the Lab is operational, and that equipment always is performing accordingly.

R&D laboranter til kemisk analyselaboratorie

Er du interesseret i at tage nye udfordringer op? Kunne du tænke dig at indgå i et dynamisk team, der lægger vægt på kvalitet, professionalisme og et positivt mindset?

Du vil bl.a. forberede prøver til kemisk analyse ved at følge etablerede protokoller, som kan omfatte prøvehomogenisering, formaling, vejning og fortynding.

Vi tilbyder et arbejdsmiljø, der fokuser på samarbejde og inklusion, hvor medarbejderne opfordres til at dele ideer, samarbejde om projekter og bidrage til virksomhedens succes.

Senior Research Technician

Do you want to work with data and HPLC analysis?

You will spend most of your time on HPLC analysis in our modern laboratory, which is designed to provide the best technologies and optimal working conditions.

Collaborating cross-functionally with our research scientists on both daily operations and projects, you will:

• Perform analytical method development in close collaboration with the responsible scientists
• Support formulation development studies with analyses

Equipment Professional – Wash and Sterilization, Freeze dryer

Kunne du tænke dig at blive en del af et stærkt team og arbejde på en nybygget fabrik, med udstyr til sterilisation, frysetørring, fyldning, inspektion og pakning? Du vil komme til at understøtte den nuværende udstyrsansvarlige, som vil sørge for den nødvendige oplæring.

Du vil blive en del Technical Support og vil være tilknyttet området for autoklaver, vaskemaskiner og vores frysetørrer. Her vil du være med til at sikre proces, procedurer, GMP, og generelle forbedringer på udstyret.

Erfaren QA-Specialist – til frigivelse af produkter

Stillingen byder på et bredt udsnit af QA-opgaver og flere kan komme til, så du får gode muligheder for at videreudvikle dine QA-kompetencer.

Opgaverne:

• Selvstændig frigivelse af PKC’s produkter og behandling af afvigelser og håndtering af ændringssager
• Sparringspartner for QA-gruppen, QC-gruppen og produktionen

Du får ansvar for og stor medbestemmelse over dine opgaver. Der er tid til fordybelse, men der er også dage, hvor det går rigtig stærkt, og opgaverne blev andre end dem, du havde planlagt og forventet.

(Senior) Drug Substance Specialist

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Single Use Systems Professionals

Som Single Use Systems Professional arbejder du med at forbedre Drug Substance produktionens Single Use systemer. Det kan eks. være i forbindelse med en eksisterende item, der ikke fungerer optimalt eller udgår. Du skal derfor søge efter brugbare erstatninger på markedet og kommunikere med leverandørerne og i samarbejde med processpecialisterne designe nye løsninger.

Du bliver en del af en afdeling på i alt 14 kolleger og i dette team er der 7, hvor alderen ligger omkring 30-45 år. Som ny medarbejder bliver du sidemandsoplært og kommer til at følge interne kurser. Du får også en Buddy fra teamet, som du kan støtte dig til.

Kemiker til QC med GMP-erfaring

Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.

Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.