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11 jobannoncer matcher din søgning 11 jobannoncer fundet
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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.
GMP Material Scientist
Are you motivated by challenges and thrive in a fast-paced environment?
Associate Director in RA CMC & Devices
Would you like to be part of an area where we bring treatments to patients?
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?
QA Assistent
Kunne du tænke dig at være med til at sikre kvaliteten af lægemiddelprodukter til kliniske forsøg?
Scientist - Mammalian Cell Cultivation
Do you have experience with mammalian cell cultivation at a pilot scale or motivated to learn?
QA Manager in CMC QA
Are you interested in leading a team of dedicated and specialized QA Employees, making a significant impact in leadership?
Senior QA Professional with CMO expertise
Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA?