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40 jobannoncer matcher din søgning 40 jobannoncer fundet
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(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.
Senior QA Specialist
You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.
We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.
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.
Regulatory Affairs Clinical Specialist
Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.
Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.
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.
Area Manager EMEA
Vil du være en del af en spændende vækstrejse inden for innovative probiotika?
Som Area Manager vil du være en nøgleperson i vores mission om at levere førsteklasses probiotiske løsninger til vores kunder.
Din rolle vil omfatte at identificere salgsmuligheder, udvikle salgsstrategier og opbygge stærke forretningsrelationer samt præsentere skræddersyede løsninger til vores B2B-kunder i udvalgte lande inden for EMEA.
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.
Experienced GMP Partner
Are you passionate about compliance, structure, and continuous improvements?
Manager of Safety Surveillance Early Development
Do you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk?
Senior International Medical Manager
Are you a Medical Doctor with an interest in clinical development of pharmaceutical drugs, medical devices and digital health?
Senior Regulatory Affairs CMC Professional
Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area?
Senior Regulatory Affairs Professional
Do you want to play a key role in accelerating the development of our patient-focused products?
Scientific Publications Manager
If you have a great interest in scientific communication and enjoy interacting with global key opinion leaders in a dynamic working environment, then please read on!
Clinical Pharmacology Specialist
Are you passionate about clinical pharmacology and drug development?
