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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 Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Senior Technical Writer - Regulatory (CMC)
You will join the Technical Writing team within Global Regulatory Affairs. We are responsible for global regulatory CMC writing of regulatory documents in applications for new approvals, worldwide market expansions, and product lifecycle activities. We work with a variety of pharmaceutical products, including small molecules, peptides, biologicals, recombinant products, and gene therapy.
Stepping into an informal and collaborative environment, you will have close interfaces with many different disciplines, including Global Pharmaceutical R&D, manufacturing sites, Product Supply, Quality Assurance, Ferring affiliates, and development sites around the world.
Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)
Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!
As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.
Kontorelev til Contract Management & Compliance
Er du klar til at kickstarte din karriere som kontorelev i en engageret og udviklingsorienteret afdeling?
Chemical/Process Engineer for CMC Chemical Development
Are you motivated by joining an expanding area within chemical manufacturing, which is strategically important for shaping the future of Novo Nordisk?
Associate Director in RA CMC & Devices
Would you like to be part of an area where we bring treatments to patients?
Senior Research Scientist
Would you like to be part of a team that plays a significant role in the innovative pipeline of creating new medications through the implementation of advanced technologies?
Er du vores nye serviceassistent i Aalborg? (cleaning staff)
Vi søger dig, der kan arbejde morgentimer fredag-mandag ca. 6 timer pr. dag.
Procesteknolog/Tekniker til kultiveringsteam
Er du uddannet procesteknolog, tekniker eller lignende, og har du erfaring fra procesanlæg og produktion under GMP?
QA Professional, Team Facility and Equipment
Are you eager to play an important role in ensuring the quality and safety of products for clinical trials?
General IT Project Manager
Do you see yourself as a project manager within the area of in information modelling and IT?
IT System Manager
Are you ready for a unique opportunity to shape the validation direction for Laboratories of the Future in Novo Nordisk?
Analytical Project Manager
Are you ready to apply your project management experience in an exciting organization, where you will get challenged, grow, and expand your capabilities to the fullest?
Automatiktekniker til Klinisk Pakkeproduktion
Har du lyst til at arbejde med Novo Nordisks nye spændende lægemiddelprodukter?
Program Director for M&A Business Integrations
Novo Nordisk is expanding its manufacturing network through acquisitions of new production technology platforms.
QA Assistent
Kunne du tænke dig at være med til at sikre kvaliteten af lægemiddelprodukter til kliniske forsøg?
Global Regulatory CMC & Device Lead
We are rapidly expanding our product and project pipeline in Novo Nordisk and are looking for an experienced Global Regulatory CMC &...