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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 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.
MS&T Program Manager
We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.
As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.
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?
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?
Associate Aseptic Manager
Are you ready to take on a challenging role in managing our new production lines?
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 Professional for Environmental Monitoring
Are you experienced in environmental monitoring in production area?
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?
Product Stability Scientist
Are you passionate about working with solid dose products and other emerging technologies?
Senior QMS Professional
Are you ready to make a difference for people living with diabetes and be part of the tablet production in Emerging Technologies (ET).
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...
Recovery and Purification Supporter
Are you someone who excels in a dynamic and fast-paced setting where teamwork is essential for success?