17 jobs voor clinical support engineer gevonden

Clinical Pharmacology and Pharmacometrics (CPP) is an integrated part of the Global Development organization within Johnson & Johnson Innovative Medicines.We work in cross disciplinary compound development teams and apply clinical pharmacology principles and pharmacometrics methodologies across the R&D portfolio to enable optimal decision making in drug development at the earliest time point and in the most efficient manner.CPP Summer Internships are available for Pharm.

The Production Quality Assurance (PQA) Engineer manages quality activities within the Production Line to guarantee deployment of production quality strategy..1.

Your responsibilities include ensuring timely support for clinical and commercial readiness while maintaining the highest quality and safety standards.BedrijfsomschrijvingOur client is on a mission to revolutionize healthcare by combatting life threatening diseases with groundbreaking biotechnology.Situated in the vibrant heart of New Jersey, their global influence extends far and wide as they pioneer advanced cell therapies across various technology platforms.

Global Planview Adaptive.Work Administrator.Summary.The Global Planview Adaptive.

Onze klant, Legend Biotech, gevestigd in Zwijnaarde, is een wereldwijd biotechnologiebedrijf dat de innovatieve CAR T celtheraptie naar Gent brengt.Het Legend Biotech team maakt hiermee dagdagelijks het verschil in het leven van vele patiënten die lijden aan kanker en andere levensbedreigende ziektes..

The MSAT Scientist is a member of the Analytical Science and Technology (AST) team in the Recombinant Mammalian Drug Substance (DS) function within the global Manufacturing Science, Analytics and Technology (MSAT) organization and is based in Sanofi Geel biopharmaceutical manufacturing site..The Recombinant Mammalian DS platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network.

We, at Sanofi, are there beside people in need, as a health journey partner+100,000 employees, representing 142 nationalities90 countries where Sanofi is present, providing healthcare solutions in 170 countries69 manufacturing sites in 32 countries21 Research and Development sites comprising medicines, clinical research and vaccinesJobomschrijvingThe MSAT Scientist is a member of the Analytical Science and Technology (AST) team in the Recombinant Mammalian Drug Substance (DS) function within the global Manufacturing Science, Analytics and Technology (MSAT) organization and is based in Sanofi Geel biopharmaceutical manufacturing site The Recombinant Mammalian DS platform function within global MSAT is the owner of Life Cycle Management of mammalian cell culture based DS Processes within Sanofi biologics manufacturing network.We deliver innovative, robust, and cost effective next generation processes, enable launch of new products, and provide commercial manufacturing/Quality Control support.

As a CAR T Operations Supervisor, you are responsible for the daily production process of personalized cell therapy, both for clinical and commercial purposes, in a sterile c.GMP environment.

Our client, Legend Biotech, based in Zwijnaarde, is a global biotechnology company bringing the innovative CAR T cell therapy to Ghent.With this, the Legend Biotech team makes a daily difference in the lives of many patients suffering from cancer and other life threatening diseases..

The CAR T Operations Supervisor is an exempt level position working within Technical Operations team, responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile c.GMP environment.

Onze klant, Legend Biotech, gevestigd in Zwijnaarde, is een wereldwijd biotechnologiebedrijf dat de innovatieve CAR T celtheraptie naar Gent brengt.Het Legend Biotech team maakt hiermee dagdagelijks het verschil in het leven van vele patiënten die lijden aan kanker en andere levensbedreigende ziektes..

Join our client’s team and play a crucial role in their cutting edge biotechnology advancements..As a CAR T Operations Technician, you'll be responsible for conducting essential CAR T process operations while ensuring compliance with safety policies and quality standards.

As CAR T Operations Expert, you will be part of the manufacturing operations team responsible for production of CAR T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (c.GMP) cleanroom environment.

The ProgramThe Johnson & Johnson Supply Chain internship offers you the opportunity to get a first glimpse ofyour potential future career and to apply your academic knowledge in a real life supply chaincontext.Our internship is a great way to get noticed within the world of J&J.As an intern you will be part of a team and get to experience the daily challenges we face in Johnson & Johnson Supply Chain.

As a laboratory technician, you are responsible for examining the blood samples, entering the data and processing and analyzing it.BedrijfsomschrijvingThe company is a global biotechnology firm dedicated to treating, and one day curing, life threatening diseases.Headquartered in Somerset, New Jersey, they are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T cell, T cell receptor (TCR T), and natural killer (NK) cell based immunotherapy.

As a laboratory technician, you are responsible for examining the blood samples, entering the data and processing and analyzing it.Client DetailsThe company is a global biotechnology firm dedicated to treating, and one day curing, life threatening diseases.They are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T cell, T cell receptor (TCR T), and natural killer (NK) cell based immunotherapy.

YOUR MISSION.As QA/RA Manager, your primary mission will be to support XEOS in quality and regulatory affairs matters and become our in house expert in navigating regulatory complexities and in maintaining our quality management system By ensuring compliance and strategic direction, you will play an important role in advancing our mission of bringing groundbreaking medical technologies to the operation room..