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QC-medarbejder med passion for IT
Du vil være QC’s nøgleperson i LIMS-projektgruppen hvor vi skal implementere LabVantage som vores LIMS-system.
Du vil være ansvarlig for at implementere og understøtte designet af vores LIMS-system ved at oprette og vedligeholde de mesterdata, som udgør rygraden i vores LIMS.
Hos os får du en chance for at være en del af et dedikeret og talentfuldt team i en organisation, hvor professionalisme møder passion. Vi vægter dog også en god portion humor i dagligdagen.
Manufacturing Associate - Operator
We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.
We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.
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.
SAP Master Data Specialist
Do you want to be a part of Process Support in a company with a unique impact on global healthcare?
You will be coordinating SAP production master data activities throughout the organization in order to achieve safe and predictable product implementation, maintenance, and decommissioning.
Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop and grow your own skills.
Senior Vice President, Global Chief Medical Office
We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).
In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.
Manager Virus Production
Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?
Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.
Coordinator til produktsikkerhed
Sætter du pris på sikre produkter, og vil du gerne være med til at garantere, at de varer, der bliver solgt til dig og mig ude i butikkerne, er i orden og lever op til lovgivningen?
Dine opgaver:
- Med afsæt i Schous testdatabase, at opstille testkrav til produkter, validere leverandørens testrapporter og udarbejde overensstemmelseserklæringer og udarbejde interne sales check.
- Kontrollere produktmærkningskrav og produktvejledninger.
- I samarbejde med specialister og indkøbere at medvirke til produktrisikovurderinger.
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
Senior Specialist til QC hos Xellia Pharmaceuticals
Drømmer du om mere ansvar, med forskelligartede opgaver, og har du en passion for mikrobiologi? Vil du spille en central rolle i Xellias produktionen af livsvigtig antibiotika?
Som senior specialist vil du blive faglig ansvarlig for vores count release-laboratorie, som bl.a. udfører TVC- og LAL-analyser. Derudover vil du indgå i tæt samarbejde med vores sterile produktioner angående EM, hvor de nye Annex 1-krav stiller øgede krav til vores compliance, som du vil spille en vigtig rolle i.
Professional, Visual Inspection
Kunne du tænke dig at være med i et spændende eventyr hos en fabrik i rivende udvikling? Har du erfaring med GMP i lægemiddelindustrien?
Du vil blive en del af Production Support og vil være tilknyttet visuel inspektionsprocessen, hvor du vil være med til at sikre proces, procedurer, GMP og generelle forbedringer på vores proces.
Application Specialist – Beverages
Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?
You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.
Biocompatibility Specialist
We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.
This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.
Laborant til mikrobiologisk team
Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?
Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.
Training Partner
Are you passionate about designing high impact training to improve ways of working?
The role will focus on re-designing the training related to onboarding our professionals working directly with our operation, our Operators, and our Laboratory Technicians.
You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words.
Technician, EMA Solids Support Team
Welcome to Solid Support Team 13 skilled process engineers and technicians responsible for quality, introducing new products, throughput, and optimizing the products.
In this role you’ll make an impact by:
- Responsible technician for the MG-coating line, ensuring smooth and efficient coating processes for granulating with MnTACN
- Coordinate the steering system changes, bridging the gap between process engineers, technicians, and programmers to optimize operational efficiency.
Technical Specialist, Product Quality, Nourish (Maternity cover, 12 months)
Are you an enthusiastic, motivated and detail-oriented professional with a desire to work in a team of colleagues with great technical competencies within production, regulation and processes?
Your core responsibilities:
- Handling deviations for products manufactured at our factories.
- Handling of product quality related complaints.
- Coordinate and implement customer-specific requirements. Maintenance of master data in various IT systems, including SAP.
QC Laboratory Technician
Har du lyst til en hverdag fyldt med spændende opgaver, fokus på høj produktkvalitet og med en stor grad af ansvar? Synes du, det er sjovt at arbejde med ingredienser til en bred vifte af fødevarer?
Primære arbejdsopgaver:
- Analyser af råvarer, mellemvarer og færdigvarer, herunder kemiske og sensoriske analyser
- Frigivelse af råvarer, mellemvarer og færdigvarer
- Udarbejdelse af analysecertifikater til vores kunder
Procesoperatør
Er du klar til at gøre en stor forskel i en dansk virksomhed med stærk global tilstedeværelse?
Du vil få ansvaret for at overvåge hele fremstillingsprocessen fra modtagelse af råvarer til fremstilling af det færdige produkt.
Dine primære opgaver som procesoperatør vil derfor være:
- overvågning og betjening af anlæggene, herunder optimering, justering, fejlfinding og prøvetagning af færdigvarer
- analyse af produkter for at sikre høj kvalitet
Trives du i et dynamisk miljø med højt tempo? Så er det muligvis dig, vi leder efter til denne spændende stilling.
Project Manager
Trives du med at arbejde sammen med dedikerede og erfarne kollegaer, der brænder for at udvikle og producere medicinske hjælpemidler til børn og unge med funktionsnedsættelse?
Kan du samtidig se dig selv som projektleder i en specialiseret verden, hvor innovativt design, teknik og brugervenlighed skal gå op i en højere enhed, så er det dig, vi søger i vores R&D-afdeling i Gedved ved Horsens.
Project Manager - Sustaining Engineering & PMO
We are looking for an experienced Project Manager to join our PMO, Technology and Innovation. You will lead sustaining engineering projects with multidisciplinary teams of engineers and specialists.
You will apply your project management, people leadership, and technical skills to qualify and implement changes to existing products e.g., material changes or quality updates. Together with your team you create clear ambitious plans and ensure projects are delivered on time with agreed quality, scope and cost.