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11 jobannoncer matcher din søgning 11 jobannoncer fundet
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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.
Clinical Site Manager
Are you looking to make a significant impact on ensuring oversight of our outsourced clinical studies in Ferring Pharmaceuticals? Do you thrive in a global role that requires cross-functional collaboration?
In this role you will solidify the implementation of the Clinical Site Manager role. This role was recently introduced as being responsible for providing sponsor oversight of clinical site monitoring (outsourced to a CRO) and establishing strong relationships with clinical sites to ensure delivery of high-quality and timely clinical trials.
In this role you will be working closely with counterparts in the US and stakeholders at our International PharmaScience Center (IPC) in Copenhagen.
Senior Specialist, Visual Inspection
Er du interesseret i at blive en del af en nystartet fabrik under hurtig udvikling? Har du erfaring med visuel inspektion inden for lægemiddelindustrien? Hvis ja, så er der en fremragende mulighed for at blive en del af vores eventyr hos Bavarian Nordic.
Vi er på udkig efter en specialist i visuel inspektion til at indgå i vores back office team inden for produktionssupport. Du vil spille en central rolle i håndteringen af vores proces for visuel inspektion.
Senior QA Specialist
As a member of our professional QA team, you'll be responsible for ensuring that our release and quality systems meet regulatory and industry standards. Working alongside a team of 8 QA Specialists and 2 student workers, you'll report directly to the QA Manager.
Your responsibilities will include:
- Reviewing and approving batch documentation, raw materials, process solutions, API intermediates, and final API
- Releasing materials and APIs
Sterile Filtration Professional
Do you have in depth experience within Sterile Filtration of drug product, and a service mindset to support global manufacturing of Injectable Finished Product?
Senior Utility Professional
Would you like to make an impact on aseptic pharma production with your clean utility and cooling, ventilation, and raw steaming expertise?
Supporter for Quality Control Laboratory
Do you want to be a part of the quality control of products in the Biotech and Rare Disease Quality Control (QC) portfolio?
GMP Professional
Are you passionate about having a central role in a dynamic department with tasks that involve close collaboration with many stakeholders on a daily basis?
Health & Safety Specialist
Are you ambitious about promoting health, safety (HS), and prevention throughout the entire value chain, coupled with a talent for...
Manager in R&D Quality
Are you looking for a dynamic and challenging management role within Clinical Compliance in R&D Quality, where you can use your skills...
Senior GCP Advisor Specialist
Looking for a dynamic and challenging role within clinical process management?
