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37 jobannoncer matcher din søgning 37 jobannoncer fundet
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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.
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
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.
Senior Engineer Device Manufacturing
Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?
Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.
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.
QA Tekniker
Vil du være en del af QA Operations Support i en virksomhed med en unik indvirkning på det globale sundhedsvæsen?
Grib denne mulighed for at blive en del af vores hurtigt voksende virksomhed, som er klar til at investere i dig. Hos os vil du ikke blot få muligheden for at påvirke produktionen af vores produkter – du får også mulighed for at udvikle dig i vores QA Operations Support Team, hvor vi ekspanderer for at kunne følge med og fortsat at kunne levere den ønskede høje kvalitet.
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.
Together with the rest of the team, you will be responsible for the daily support of our production lines. You will learn our processes in detail and gain a good overview of the documentation used in production.
Lead Automation Engineer til Pharmadivisionen
Har du en god procesforståelse og erfaring med at arbejde i pharmabranchen, kan du måske se dig selv som Lead Automation Engineer i Pharmadivisionen.
Vi søger to nye kollegaer med en stærk automationsfaglig erfaring og kendskab til at arbejde med sterile processer. Du bliver en del af afdelingen: C&Q/Automation – en nyere afdeling som vi er godt i gang med at opbygge. På nuværende tidspunkt består den af syv dedikerede medarbejdere, der arbejder med commissioning, automation og test af anlæg. Her vil du indtage en central rolle som specialist på automationsområdet, og du vil få rig mulighed for at være med til at udvikle C&Q/Automation-afdelingen.
Senior Commissioning & Qualification Engineer
Vi søger en Commissioning & Qualification Engineer, der elsker at blive udfordret inden for sit fag, og som deler vores passion for at arbejde med pharma.
Du vil komme til at arbejde med projekter inden for idriftsættelse, test og fejlfinding på anlæg - hovedsageligt på projekter i pharmasektoren. Stillingen berører stort set alle aspekter inden for idriftsættelse, og det er vigtigt for os, at du har en solid erfaring med maskin- og processtyring samt praktisk idriftsættelse.
Du får rig mulighed for at være med til at præge udviklingen af afdelingen, hvor vi gør en stor indsats for at skabe et godt sammenhold i en travl hverdag.
GMP Material Scientist
Are you motivated by challenges and thrive in a fast-paced environment?
Statistical Specialist
Are you a highly experienced statistician looking for an opportunity to use your statistical knowledge and quality mindset to bring clinical projects to registration and market?
Corporate Vice President (CVP) Clinical Reporting within Development
Are you a seasoned leader with experience from a large, complex, and international pharmaceutical company?
Formulation Professional
Do you have in depth experience within formulation of drug product, and a service mindset to support global manufacturing of Injectable Finished Product?
Senior Regulatory Affairs Professional
Are you able to cut through complexity and drive regulatory strategies for high-impact projects?
Associate Director in RA CMC & Devices
Would you like to be part of an area where we bring treatments to patients?
GCP Advisor Specialist
Do you dream of using your GCP knowledge, clinical research experience and perhaps GCP audit experience and last but not least your quality...
Senior Director in Data Orchestration
Can you make a difference in drug development through data?
Senior Manager
Are you an empathetic and empowering leader ready to bring your leadership career to the next level?
Associate Regulatory Professional for CTA Management
Are you adept at planning, coordination, problem-solving, and collaboration across the organization?