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16 jobannoncer matcher din søgning 16 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
QA-assistent med GMP-erfaring
Vi søger vi en erfaren og selvstændig QA-assistent, der har lysten til at være en del af udviklingen af en nystartet state-of-the-art-bioethanol-produktionsvirksomhed.
Dine primære arbejdsopgaver vil være:
- Vedligeholdelse af QMS-system, instruktioner, vejledninger osv.
- Review af batchdokumentation.
Du tilbydes en attraktiv og konkurrencedygtig lønpakke med pension og sundhedsforsikring.
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.
QA Specialist
You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.
You will have the opportunity to:
- Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
- Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.
Medical Scientific Liaison Renal Acute
Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company.
Development PKPD Specialist
Are you a scientist with flair for mathematical modelling and knowledge of pharmacology, biology or physiology?
Upstream Support Specialist
Would you like be responsible for providing technical assistance within process design and process documentation?
Recovery and Purification Supporter
Are you someone who excels in a dynamic and fast-paced setting where teamwork is essential for success?
Senior Director in Data Orchestration
Can you make a difference in drug development through data?
Miljøsupporter
Brænder du for at skabe gode realtioner med mennesker på tværs af faggrupper?
Product Specialist - Oral Solid Dosage Forms
Are you passionate about providing expert product knowledge and setting the direction for future tablet production to the benefit of our patients?
QA Assistent
Kunne du tænke dig at være med til at sikre kvaliteten af lægemiddelprodukter til kliniske forsøg?
Senior Cultivation Process Supporter for API Production
Are you passionate about driving the cultivation process within API Production?
Product Responsible
Are you ready to harness your skills in design control and to take up responsibility for some of the largest products in the market?
Quality Assurance Analyst - Pharmaceuticals and Hormonal Contraceptives, Supply Chain Management Unit (SCMU), Copenhagen
The Quality Assurance Analyst position is within the Product Quality Assurance Team in the UNFPA Supply Chain Management Unit (SCMU).
